1. Structural Biology and Molecular Biophysics

Inhibition of the proton-activated chloride channel PAC by PIP2

  1. Ljubica Mihaljević
  2. Zheng Ruan
  3. James Osei-Owusu
  4. Wei Lü  Is a corresponding author
  5. Zhaozhu Qiu  Is a corresponding author
  1. Department of Physiology, Johns Hopkins University School of Medicine, United States
  2. Department of Structural Biology, Van Andel Institute, United States
  3. Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, United States
https://doi.org/10.7554/eLife.83935
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Cite this article
  1. Ljubica Mihaljević
  2. Zheng Ruan
  3. James Osei-Owusu
  4. Wei Lü
  5. Zhaozhu Qiu
(2023)
Inhibition of the proton-activated chloride channel PAC by PIP2
eLife 12:e83935.
https://doi.org/10.7554/eLife.83935
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Abstract

Proton-activated chloride (PAC) channel is a ubiquitously expressed pH-sensing ion channel, encoded by PACC1 (TMEM206). PAC regulates endosomal acidification and macropinosome shrinkage by releasing chloride from the organelle lumens. It is also found at the cell surface, where it is activated under pathological conditions related to acidosis and contributes to acid-induced cell death. However, the pharmacology of the PAC channel is poorly understood. Here, we report that phosphatidylinositol (4,5)-bisphosphate (PIP2) potently inhibits PAC channel activity. We solved the cryo-electron microscopy structure of PAC with PIP2 at pH 4.0 and identified its putative binding site, which, surprisingly, locates on the extracellular side of the transmembrane domain (TMD). While the overall conformation resembles the previously resolved PAC structure in the desensitized state, the TMD undergoes remodeling upon PIP2-binding. Structural and electrophysiological analyses suggest that PIP2 inhibits the PAC channel by stabilizing the channel in a desensitized-like conformation. Our findings identify PIP2 as a new pharmacological tool for the PAC channel and lay the foundation for future drug discovery targeting this channel.

Editor's evaluation

The recently identified Proton-Activated Chloride (PAC) channel is ubiquitously expressed and has important roles in intracellular organelles and its function in the plasma membrane is associated with human pathologies. Combining electrophysiology, site-directed mutagenesis, lipid pharmacology, and single particle cryo-electron microscopy, this valuable study provides solid evidence to identify a site on the extracellular half of the transmembrane domain of PAC channels that could be occupied by PIP2 and related lipids to promote channel desensitization. These findings are relevant because pharmacological information for this important ion channel is absent.

https://doi.org/10.7554/eLife.83935.sa0

Introduction

Proton-activated chloride channel PAC (also known as acid-sensitive outwardly rectifying anion channel or ASOR) is an evolutionarily conserved membrane protein with ubiquitous expression across different tissues. Since the recent discovery of its molecular identity (Yang et al., 2019; Ullrich et al., 2019), PAC has been implicated in important biological functions, such as endosomal trafficking and macropinocytosis (Osei-Owusu et al., 2021; Zeziulia et al., 2022). In the endosome, low luminal pH activates PAC to mediate chloride efflux from the lumen. Thereby, PAC actively regulates luminal acidification by depleting the counter ion, chloride, and preventing proton accumulation in the endosome (Osei-Owusu et al., 2021). During macropinocytosis PAC mediates the shrinkage of macropinosomes by releasing chloride into the cytoplasm (Zeziulia et al., 2022). In addition to localizing to the intracellular organelles, PAC also traffics to the plasma membrane, where it is involved in several pathological conditions associated with acidosis. For example, upon ischemic stroke, PAC is activated by drops in tissue pH, allowing the entry of chloride into the cells. This subsequently causes cellular swelling and contributes to acid-induced brain injury (Osei-Owusu et al., 2020; Yang et al., 2019).

PAC is a homotrimer that forms a chloride-selective pore in the membrane, and it senses changes in pH via its large extracellular domain (ECD) (Deng et al., 2021; Osei-Owusu et al., 2022a; Ruan et al., 2020; Wang et al., 2022). PAC channel is closed at neutral pH and becomes activated when the pH drops below 5.5 (Yang et al., 2019). The proton binding to the ECD is directly coupled with the channel opening in the transmembrane domain (TMD) (Osei-Owusu et al., 2022a). After prolonged exposure to pH 4.6 or below, the PAC channel slowly desensitizes (Osei-Owusu et al., 2022b). The desensitization of PAC is pH-dependentthat is, under more acidic conditions, desensitization is stronger (Osei-Owusu et al., 2022b). This is regulated by several key residues localized at the ECD–TMD (Osei-Owusu et al., 2022b). For example, the E94R mutant displays fast desensitization even at pH 5.0, when the wild-type channel does not exhibit obvious current decay (Osei-Owusu et al., 2022b). In addition to the resting and desensitized structures (Ruan et al., 2020), an open conformation of PAC was recently reported (Wang et al., 2022). The transition between closed, open and desensitized PAC channel conformations involves major structural rearrangements inside the lipid bilayer (Ruan et al., 2020; Wang et al., 2022). It is now widely accepted that the membrane shapes ion channel function and structure. Lipid composition and the thickness of the membrane can directly control or fine-tune the gating of certain ion channels (Rosenhouse-Dantsker et al., 2012). However, whether the PAC channel is regulated by lipids is unknown.

The most common and best-studied lipid regulator of ion channel function is phosphatidylinositol (4,5)-bisphosphate (PIP2). PIP2 is a negatively charged phospholipid, predominantly found in the inner leaflet of the plasma membrane (Suh and Hille, 2008), with few reports that a small amount can localize to the outer leaflet as well (Gulshan et al., 2016; Yoneda et al., 2020). Although it accounts for less than 1% of the total phospholipids in the plasma membrane, it is a principal signaling molecule and an essential cofactor for ion channel function (Hansen, 2015; Suh and Hille, 2008). PIP2 binds to ion channels directly and modulates their function by facilitating channel opening, preventing current rundown/desensitization, or inhibiting channel activity (Gada and Logothetis, 2022; Suh and Hille, 2008). At least 10 different ion channel families are dependent on PIP2 for their activity (Gada and Logothetis, 2022; Suh and Hille, 2008). A handful of ion channles are negatively regulated by PIP2 (Gada and Logothetis, 2022; Suh and Hille, 2008), one of which is TMEM16B− the only chloride channel that is reported to be inhibited in the presence of PIP2 to this date (Ta et al., 2017).

Major breakthroughs have been made in recent years to characterize the structure and function of the PAC channel in biology and disease, but its regulation by endogenous molecules remains largely unexplored. PAC recently emerged as a target of interest for acidosis-related diseases, and much progress has been made to identify natural and synthetic compounds that can inhibit PAC channel (Figueroa, 2020; Okada et al., 2021; Sato-Numata et al., 2016). DIDS (4,4-diisothiocyanatostilbene-2,2-disulfonic acid), a broad-spectrum chloride channel blocker, with a half-maximal inhibition (IC50) of 2.9 µM in HEK293 cells (Okada et al., 2021) is the most commonly used PAC inhibitor. To date, arachidonic acid (IC50 of 8.9 µM; Okada et al., 2021) and pregnenolone sulfate (IC50 of 10 µM; Figueroa, 2020) are the only reported potential biological inhibitors of the acid-induced chloride currents (ICl,H) mediated by PAC, yet their mechanism and binding sites are not fully characterized. Here, we show that PIP2 potently inhibits PAC and present the first structure of PAC channel with an inhibitor. Furthermore, we elucidate the molecular mechanism by which PIP2 inhibits PAC by stabilizing a desensitized-like conformation of the channel.

Results

PIP2 inhibits PAC channel activity

Considering the widespread influence of PIP2 on ion channel function, we hypothesized that PIP2 could potentially regulate the PAC channel. To test whether PIP2 modulates PAC activity, we applied a soluble version of PIP2 lipid, dioctanoyl phosphatidylinositol 4,5 bisphosphate (diC8-PIP2), to HEK293 cells, which endogenously express the acid-induced chloride currents. Whole-cell ICl,H were detected in real-time, by perfusing the cells with an acidic solution at pH 5.0, followed by an application of 10 µM diC8-PIP2. Immediately upon adding PIP2, there was a rapid drop in ICl,H, followed by a steady decline (Figure 1A). Furthermore, this effect was reversible by washing out the soluble lipid from the cell membrane with a pH 5.0 solution (Figure 1A). Approximately 37% of the initial current amplitude was detectable after PIP2 perfusion for 150 s (Figure 1B and C). This short timescale of PIP2 action on PAC activity indicates that its effect is most likely direct. Further supporting this, PIP2 inhibited ICl,H in a dose-dependent manner, with half-maximal inhibition, IC50, of 4.9 µM (Figure 1D).

Figure 1 with 1 supplement see all
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PIP2 inhibits the PAC channel activity.

(A) Representative whole-cell current trace at + 100 mV (2 s/sweep) showing inhibition of endogenous PAC currents by bath perfusion of soluble diC8-PIP2 at 10 μM concentration. (B) PAC current densities before and after application of PIP2 for 150 s. Statistical significance was determined using a two-tailed Student’s paired t-test. (C) Representative I/V curve of pH 5-induced PAC currents before and after PIP2 treatment. (D) Dose-dependent inhibition of pH 5-induced PAC currents by PIP2 yielded a half-maximal inhibition, IC50, of 4.91 μM with a Hill slope of 1.57. Bars are reported as mean ± SEM.

Figure 1—source data 1

Data and statistics plotted in Figure 1.

https://cdn.elifesciences.org/articles/83935/elife-83935-fig1-data1-v2.xlsx

At neutral pH, the PAC channel is in its resting/closed state, and it is activated/open when the pH drops below 5.5 at room temperature (Yang et al., 2019). To examine if PIP2 exerts its effect on the PAC channel in its closed or open state, we pre-treated the cells with soluble PIP2 at pH 7.3, and then activated the channel with acid. ICl,H amplitude at pH 5.0 did not show any significant difference before and after perfusion of PIP2 at the neutral pH (Figure 1—figure supplement 1A, B). This result suggests that PIP2 may not act on the resting state of PAC and is only effective once the channel undergoes proton-induced activation or the subsequent desensitization.

Phosphates and the acyl chain synergistically contribute to PIP2-mediated PAC inhibition

To test if there is a preference among different phosphatidylinositol lipids, we used soluble (diC8) versions of lipids at 10 µM concentration and compared their inhibitory effects on pH 5.0-induced endogenous PAC currents. PI(3)P (phosphatidylinositol 3-phosphate) with a single phosphate on its inositol headgroup, inhibited PAC significantly less than either bisphosphonates, PI(4,5)P2 or PI(3,5)P2 (phosphatidylinositol (3,5)-bisphosphate) (Figure 2A). The additional phosphate on PIP3 (phosphatidylinositol (3,4,5)-trisphosphate) yielded the IC50 of 3 µM (Figure 2B). Therefore, to reach potent inhibition, a minimum of two phosphates on the inositol headgroup are required. This is additionally supported by a modest inhibitory effect of PI (phosphatidylinositol) that does not have any active headgroup phosphates (Figure 2C). Interestingly, IP3 (inositol 1,4,5-trisphosphate), a triple-phosphorylated inositol headgroup without an acyl chain, displayed a similarly modest inhibition on PAC as PI (Figure 2D). Phosphates on the headgroup are therefore necessary, but not sufficient for PAC inhibition, indicating that the lipid chain contributes to inhibitory properties of PIP2 as well. diC8-diacyl-glycerol (DAG), the lipid chain without inositol head, had no inhibitory effect on PAC (Figure 2D). Acyl chain alone is therefore not sufficient to inhibit PAC.

Figure 2
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Phosphates and acyl chain length synergistically contribute to PAC inhibition by PIP2.

(A) Percent inhibition of pH 5-induced PAC currents by different diC8-phosphatidylinositol lipids at 10 μM concentration: PI(3)P, PI(4,5)P2, PI(3,5)P2, and PI(3,4,5)P3. Statistical significance was determined using ordinary one-way ANOVA with the Dunnett post hoc test. Bars are reported as mean ± SEM. (B) Dose-dependent inhibition of PAC currents by PIP3. Bars are reported as mean ± SEM. (C) Dose-dependent inhibition of PAC currents by phosphatidylinositol (PI). Bars are reported as mean ± SEM. (D) Percent inhibition of pH 5-induced PAC currents by phosphatidylinositol lipids of different acyl chain length 10 μM concentration: Diacylglycerol (DAG), diC8-PI, IP3(1,4,5), diC6-PI(3,5)P2 and diC18:0-20:4-PI(4,5)P2. Statistical significance was assessed using ordinary one-way ANOVA with the Dunnett post hoc test. Bars are reported as mean ± SEM.

Figure 2—source data 1

Data and statistics plotted in Figure 2.

https://cdn.elifesciences.org/articles/83935/elife-83935-fig2-data1-v2.xlsx

Next, we examined the inhibitory effect of phosphatidylinositol lipids with varying chain lengths. PIP2 with two carbons less on its acyl chain, diC6-PIP2, was significantly less potent than diC8-PIP2 in inhibiting ICl,H (Figure 2D). On the other hand, full-length diC18:0-20:0 -PIP2, displayed a potent inhibition on the PAC channel, comparable to that of diC8-PIP2 (Figure 2D). Based on these results, we conclude that an acyl chain with a minimum of 8 carbons is required for potent inhibition of PAC by PIP2. Together, the number of phosphates on the inositol headgroup and lipid chain length synergistically contribute to the inhibitory potency of PIP2 to the PAC channel.

Cryo-EM structure reveals the PIP2 binding site on the PAC channel

PIP2 often binds to motifs on the intracellular side of ion channels, which contain positively charged residues that directly interact with the negatively charged phosphates on its inositol head. Indeed, the desensitized structure of PAC that we determined previously, a cluster of lipid-like density is present in the cytoplasmic fenestration area (Ruan et al., 2020). The C-terminus of TM2 has several positively charged residues, including K325, K329, K333, R335, K336, R337, K340, R341, R342, that we focused on initially and studied for their impact on PIP2 sensitivity (Figure 3—figure supplement 1A). Mutating single or triple lysine and arginine residues to alanine or making a 10-residue deletion at the C-terminal domain did not affect PIP2-mediated inhibition on pH 5.0-induced PAC currents (Figure 3—figure supplement 1B). In addition, when diC8-PIP2 was applied to the cells through an intracellular solution in the patch pipette, at a physiological concentration of 10 µM, there was no detectable change in the endogenous PAC current amplitude (Figure 3—figure supplement 1C). Similarly, ICl,H remained intact when endogenous PIP2 was depleted from the inner membrane leaflet using 100 μg/ml Poly-L-Lysine (PLL) in the patch pipette (Figure 3—figure supplement 1D). These results are surprising because endogenous PIP2 is known to be almost exclusively localized to the inner leaflet of the plasma membrane. Thus, the effect we observed with the perfusion of exogenous PIP2 may occur via inhibition of the PAC channel through a potentially unconventional mechanism.

To reveal the mechanism underlying PIP2 inhibition, we solved the cryo-EM structure of PAC in nanodiscs with 0.5 mM diC8-PIP2 at pH 4.0 to an overall resolution of 2.70 Å (Figure 3A, Supplementary file 1). The structure adopts a conformation similar to the previously reported desensitized state at low pH (Ruan et al., 2020). However, a strong branched lipid density is observed on the cryo-EM map of the PAC channel in the outer membrane leaflet, between TM1 and TM2 of adjacent subunits (Figure 3A, Figure 3—figure supplement 2, Figure 3—figure supplement 3). We suspected that the density may represent a bound PIP2 molecule, although we cannot rule out the possibility that this density may represent other types of lipids, such as phosphatidic acid. When trying to fit a diC8-PIP2 molecule into this density (Figure 3B), we found that the phosphatidyl group is reasonably well defined, with its phosphate group forming a salt bridge interaction with R93 and its two acyl tails interacting with a number of hydrophobic residues on both transmembrane helices, including W304 (Figure 3C). In contrast, the hydrophilic head group, such as inositol-4,5-bisphosphate (Ins(4,5)P2) moiety of PIP2, is not resolved and therefore not modeled. The absence of the head group may be explained by its intrinsic flexibility and/or, if it is Ins(4,5)P2, its susceptibility to radiation damage due to the negative charges it carries. Nevertheless, the local biochemical environment of the site is consistent with PIP2 binding, in which the hypothetical location of Ins(4,5)P2 is surrounded by several positively charged residues, including K97, K106, and K294 (Figure 3C). The putative PIP2 binding site is also in accordance with our observation that a higher number of negatively charged phosphates, as well as the presence of an acyl chain, contribute to stronger channel inhibition by PIP2 (Figure 2). Moreover, small, but notable, conformational changes are observed in the transmembrane helices (TM1 and TM2) upon adding PIP2, which supports the binding of PIP2 to PAC. Specifically, TM1 tilts inside by 3 Å which causes a concerted rotation motion of TM2 (Figure 3B). The pore radius profile is similar to the desensitized state of PAC without PIP2, with the smallest radius of 0.43 Å (Figure 3D). Therefore, the PIP2-bound conformation also represents a non-conductive state (Figure 3A–C).

Figure 3 with 4 supplements see all
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PIP2 binds directly to the PAC channel.

(A) Cryo-EM structure of PAC channel at pH 4.0 with bound PIP2. One subunit is shown in red with TM1 and TM2 labeled. The density corresponding to putative PIP2 is colored green. (B) The structural model of PAC channel at pH 4.0 with bound PIP2 in side view (left) and bottom-up view (right). For comparison, the PAC channel at pH 4.5 without PIP2 (PDBID: 7SQH) is shown in cyan for the bottom-up view (right). (C) A close-up view of the PIP2 binding site. (Left) Cartoon representation of the PIP2 binding site. Important residues relevant to the study of the putative PIP2 binding site, including R93, K97, H98, K106, K294, and W304, are shown in stick. Cryo-EM densities for PIP2 and the nearby residues are shown in a semi-transparent surface. The Ins(4,5)P2 group is not resolved in the Cryo-EM map and thus not modeled in the deposited structure. (Right) Surface representation of the PIP2 binding site colored with electrostatic potential. Unit in kcal/mol/e-. A full PIP2 molecule, including the hypothetically positioned Ins(4,5)P2 group, is shown in the right panel. (D) The pore profile of PAC at pH 4.0 with PIP2 (PDBID: 8FBL) and at pH 4.5 without PIP2 (PDBID: 7SQH). The smallest radius along the pore axis is 0.43 Å, suggesting that both structures are impermeable to chloride ions. (E) Mutating PIP2-binding residues to alanine significantly decreases diC8-PIP2-mediated inhibition on pH 5-induced PAC currents. The constructs were expressed in PAC KO HEK293 cells for recordings. Statistical significance was assessed using one-way ANOVA with the Dunnett post hoc test. Bars are reported as mean ± SEM. (F) Multiple sequence alignment of several PAC orthologs. Key residues that form the PIP2 binding site are labeled using green dots. Binding site residues that are not conserved in zebrafish PAC (PAC_DANRE) are indicated by red triangles. (G) Percent inhibition (mean ± SEM) of hPAC or fPAC current at pH 5.0 by 10 μM diC8-PIP2. Zebrafish PAC (fPAC) shows significantly less inhibition by PIP2 compared to human PAC. Statistical significance was determined using a two-tailed Student’s unpaired t-test. (H) Mutating zebrafish PAC residues to the corresponding human PAC residues, M94R, N98K and Q295K, significantly increases the inhibition by PIP2 in comparison to the wild-type zebrafish PAC. Statistical significance was determined using a two-tailed Student’s unpaired t-test. Bars are reported as mean ± SEM.

Figure 3—source data 1

Data and statistics plotted in Figure 3.

https://cdn.elifesciences.org/articles/83935/elife-83935-fig3-data1-v2.xlsx

To validate our structural model and the putative PIP2 binding site, we carried out site-directed mutagenesis and patch-clamp electrophysiological experiments. When overexpressed in PAC knockout (KO) HEK293 cells, mutation of any residues R93, K97, K106, K294, and W304 to alanine significantly relieved the inhibition by PIP2 on pH 5.0-induced PAC currents, confirming that this was indeed its binding site on the channel (Figure 3E). We also examined an adjacent residue, H98, which is not at a distance from the binding site that would allow direct interaction with PIP2. As expected, H98A mutant was still sensitive to PIP2 inhibition (Figure 3E), suggesting that PIP2 specifically recognizes the binding pocket observed in our structure. None of the mutations we tested affected the PAC channel activity, as indicated by the normal current densities and very small desensitization at pH 5.0 (Figure 3—figure supplement 1E, F). Moreover, the PIP2 binding site is unlikely to exist in the resting and activated states of PAC because the TMD, particularly TM1, undergoes significant conformational changes relative to the desensitized state, and therefore a PIP2 molecule cannot be accommodated in these states (Figure 3—figure supplement 4).

Putative PAC PIP2-binding residues are conserved amongst higher vertebrates. On the contrary, in zebrafish (Danio rerio), several PIP2-binding site residues are different, including M94, N98, and Q295 (Figure 3F). Interestingly, the zebrafish PAC channel (fPAC) was significantly less inhibited by PIP2 compared to the human PAC (hPAC) when overexpressed in PAC KO HEK293 cells (Figure 3G). To test if the reduced PIP2 sensitivity of zebrafish PAC is due to these amino acid differences, we used site-directed mutagenesis to convert zebrafish residues to the corresponding ones of the human PAC channel. Interestingly, zebrafish triple mutant M94R, N98K, Q295K (fPAC numbering) showed a significant increase in PIP2 inhibition when compared to the wild-type channel (Figure 3H, Figure 3—figure supplement 1G). This further substantiates our finding that the PIP2 binding site on the PAC channel is located in the outer membrane leaflet.

PIP2-mediated PAC inhibition correlates with the degree of channel desensitization

Since PIP2-bound PAC structure resembles the desensitized state and the PAC channel exhibits apparent desensitization at pH 4.0 (Osei-Owusu et al., 2022b) we sought to examine how pH may influence PIP2-mediated PAC inhibition by applying diC8-PIP2 at pH 4.0 when the currents stabilized after the initial fast desensitization (Figure 4A and B). The percentage of PAC inhibition by PIP2 increased significantly at pH 4.0 compared with pH 5.0 (Figure 4C). These results suggest that PIP2 inhibition is more effective when the PAC channel is already poised toward the desensitized state under more acidic conditions.

Figure 4
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PIP2-mediated PAC inhibition correlates with the degree of channel desensitization.

(A, B) Representative current traces at + 100 mV (5 s/sweep) of endogenous PAC currents at pH 4.0 and 5.0 treated with 10 μM diC8-PIP2. diC8-PIP2 was applied after desensitized current reached a plateau. (C) Percent inhibition (mean ± SEM) of PAC currents at pH 4.0 and 5.0, 100 s after perfusion of 10 μM diC8-PIP2. Statistical significance was determined using a two-tailed Student’s unpaired t-test. (D, E) Representative current traces at + 100 mV (5 s/sweep) of overexpressing PAC WT and E94R at pH 5.0 treated with 10 μM diC8-PIP2. (F) Percent inhibition (mean ± SEM) of PAC WT and E94R currents at pH 5.0, 100 s after perfusion of 10 μM diC8-PIP2. Statistical significance was determined using a two-tailed Student’s unpaired t-test.

Figure 4—source data 1

Data and statistics plotted in Figure 4.

https://cdn.elifesciences.org/articles/83935/elife-83935-fig4-data1-v2.xlsx

We recently showed that reversing the charge of E94 residue to E94R induces PAC desensitization, even at pH 5.0 (Figure 4D and E; Osei-Owusu et al., 2022b). Structurally, E94 is located in TM1, facing the opposite side of the PIP2 binding pocket. Therefore, the E94 mutation is unlikely to affect PIP2 binding directly, representing an ideal candidate to test if there is a correlation between PIP2 inhibition and channel desensitization. Indeed, we found that PIP2 exerted a much higher degree of inhibition on the E94R mutant than the WT PAC channel (Figure 4F). Because E94 is distal to the PIP2 binding site, these effects are most likely due to the altered conformational dynamics toward desensitization. It is also important to note that the desensitization of PIP2-binding mutants was not altered (Figure 3—figure supplement 1F). Together with its pH-dependency, our data suggest that PIP2 inhibition is more effective when the PAC channel is more prone to becoming desensitized.

Discussion

PAC is a novel chloride channel, and its pharmacology is still poorly studied. Here, we showed that PIP2 binds to and potently inhibits the PAC channel with an IC50 of ~4.9 µM. This value is comparable to the EC50 of other well-studied PIP2-activated ion channels, such as TMEM16A chloride channel (~3.95 µM) and Kir inward rectifying potassium channels (~4.6 µM) (Le et al., 2019; Lopes et al., 2002). Additionally, half-maximal inhibition of PIP2 binding to PAC seems to be an order of magnitude lower than the IC50 (~46 µM) of TMEM16B− the only other chloride channel known to be inhibited by PIP2 prior to this study (Ta et al., 2017), although we noticed that this study also reported a relatively high EC50 (~53 µM) for TMEM16A (Ta et al., 2017). It is worth noting that the Hill coefficient of PIP2-mediated inhibition is estimated to be 1.57, suggesting that a cooperative mode of binding for PIP2 (Figure 1D). Our structural analysis further showed that the PIP2 binding site in PAC is located on the extracellular side of the TMD, unlike other ion channels known to be regulated by PIP2, which bind PIP2 on the intracellular side of the TMD.

Our data indicate that the degree of PIP2-mediated PAC inhibition correlates with channel desensitization. The prevalence of desensitized PAC state at pH 4.0 (Figure 4A) and in the E94R mutant (Figure 4F) facilitates the inhibitory effect of PIP2 on PAC. PIP2-mediated PAC inhibition under these conditions is more effective likely because the desensitized conformation becomes more prevalent, and the binding sites become more accessible. In contrast, under less acidic conditions most of the channels adopt the open/resting states, resulting in less inhibition by PIP2. Together, our results suggest that PIP2 achieves its inhibitory effect by altering the free energy landscape to favor the desensitized state of the PAC channel (Figure 5).

Figure 5
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A proposed model of PAC inhibition by PIP2.

PAC channel adopts resting/open/desensitized states depending on the acidity of the environment. PIP2 selectively binds and stabilizes the desensitized conformation of PAC on the extracellular side of the membrane, altering the conformational/free energy landscape of the channel. As a result, in the presence of PIP2, a significant portion of PAC will be restricted in the desensitized conformation, leading to channel inhibition.

Furthermore, we characterized pharmacological properties that contribute to phosphatidylinositol inhibitory potency on PAC. PIP3 displayed the strongest inhibition of PAC, while IP3 had a negligible effect (Figure 2). A higher number of phosphates and a longer acyl chain increase the inhibitory potency of the lipid. This indicates that the negative charge on the inositol head, as well as acyl chain insertion into the membrane, synergistically contribute to the lipid binding and stabilization of the desensitized channel state.

PIP2 is primarily localized in the cytosolic side of the plasma membrane. However, a few studies report that a small portion of PIP2 can be detected on the extracellular side (Gulshan et al., 2016; Yoneda et al., 2020). In RAW264.7 macrophages and baby hamster kidney (BHK) fibroblasts, ATP-binding cassette transporter A1 (ABCA1) facilitates the redistribution of PIP2 from the inner to the outer leaflet of the plasma membrane (Gulshan et al., 2016). Furthermore, in freshly isolated mouse bone marrow cells, PIP2 is localized on the cell surface (Yoneda et al., 2020). Binding of PI, and potentially PIP2, in the outer membrane leaflet has previously been observed in the structure of Na+/H+ exchanger (NHA2), mediating its activity through stabilization of dimer interface, a mechanism distinct from the one described here. Furthermore, the binding of PIP2 to NHA2 is yet to be confirmed in a physiological context (Matsuoka et al., 2022).

The PIP2-binding pocket on the extracellular side of the PAC channel is physiologically unusual. It is therefore unlikely, albeit not impossible, that inhibition of PAC by PIP2 occurs in a physiological setting. Considering the recent discovery of PAC and its wide tissue distribution, we speculate that PIP2 could be negatively regulating PAC in the outer leaflet of the plasma membrane in specialized cells, or under certain conditions that are currently unknown to us. For example, the PAC channel localizes to endosomes and macropinosomes of macrophages. The inner membrane of these intracellular organelles is topologically equivalent to the outer leaflet of the plasma membrane. Some pathogens enter the cells via endocytosis or macropinocytosis and escape degradation in these compartments via fusion of their membrane with the membrane of the organelle. The envelope of some pathogens is enriched in PIP2, such as in the human immunodeficiency virus (HIV; Mücksch et al., 2019). Therefore, we speculate that PIP2 could potentially be found in the inner membrane of endosomes during fusion with pathogenic membranes, where it inhibits PAC activity and modulates lumen acidification. However, it is also possible that PIP2-binding site on PAC potentially acts as a proxy for another ligand that has yet to be determined.

In conclusion, to our knowledge, PIP2 is the first PAC channel modulator with a characterized binding site and mechanism of action. Although its physiological significance remains elusive, the novel extracellular PIP2-binding pocket for targeted inhibition of PAC can be exploited for the design of PAC inhibitors that do not have to be cell-permeable. Furthermore, we describe pharmacological properties necessary for PAC inhibition, which include a stable insertion into the membrane and a negative charge that interacts with the positively charged cluster of residues on the pocket. These insights provide a useful tool for the future design of potential therapeutics for acidosis-related diseases implicating the PAC channel.

Materials and methods

Key resources table
Reagent type (species) or resourceDesignationSource or referenceIdentifiersAdditional information
Gene (Homo sapiens)hPACdoi:10.1126/science.aav9739NP_060722/Q9 H813
Gene (Danio rerio)fPACdoi:10.1126/science.aav9739NP_001278691/Q7SY31
Recombinant DNA reagentpEGC-hPAC
(plasmid)		doi:10.1038/s41586-020-2875-7
Recombinant DNA reagentpIRES2-EGFP-hPAC (plasmid)doi:10.1126/science.aav9739
Recombinant DNA reagentpIRES2-EGFP-fPAC (plasmid)This paperIn the cell culture section of Materials and methods in this paper
Recombinant DNA reagentpEGC-hPACdoi:10.1038/s41586-020-2875-7
Cell line (Homo sapiens)HEK293TATCCCat#:CRL-3216
Cell line (Homo-sapiens)tsA-201Sigma AldrichCat#: 85120602Cell line (Homo-sapiens)
Cell line (Homo sapiens)PACC1 KO HEK293Tdoi:10.1126/science.aav9739
Chemical compound, drug08:0 PI (1,2-dioctanoyl-sn-glycero-3-phospho-(1'-myo-inositol) (ammonium salt))Avanti Polar LipidsCat#:850181 P
Chemical compound, drug08:0 PI(4,5)P2 (1,2-dioctanoyl-sn-glycero-3-phospho-(1'-myo-inositol-4',5'-bisphosphate) (ammonium salt))Avanti Polar LipidsCat#:850185 P
Chemical compound, drug08:0 PI(3,5)P2 (1,2-dioctanoyl-sn-glycero-3-phospho-(1'-myo-inositol-3',5'-bisphosphate) (ammonium salt))Avanti Polar LipidsCat#:850184 P
Chemical compound, drug08:0 PI(3)P (1,2-dioctanoyl-sn-glycero-3-(phosphoinositol-3-phosphate) (ammonium salt))Avanti Polar LipidsCat#:850187 P
Chemical compound, drug06:0 PI(3,5)P2 (1,2-dihexanoyl-sn-glycero-3-phospho-(1'-myo-inositol-3',5'-bisphosphate) (ammonium salt))Avanti Polar LipidsCat#:850174 P
Chemical compound, drug18:0-20:0- PI(4,5)P2 (1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1'-myo-inositol-4',5'-bisphosphate)) (ammonium salt)Avanti Polar LipidsCat#:850165 P
Chemical compound, drugIP3(1,4,5) (D-myo-inositol-1,4,5-triphosphate (ammonium salt))Avanti Polar LipidsCat#:850115 P
Chemical compound, drug08:0 DG (1,2-dioctanoyl-sn-glycerol)Avanti Polar LipidsCat#:800800O
Chemical compound, drugPoly-L-Lysine (PLL)Sigma-AldrichCat#:26124-78-7
Commercial assay or kitLipofectamine 2000InvitrogenCat#:11668–019
Commercial assay or kitQuikChange II XL site-directed mutagenesisAgilent TechnologiesCat#:200522
Software, algorithmClampfit 10.7Molecular devices
Software, algorithmGraphPad Prism 9GraphPad
Software, algorithmClustal Omegahttps://www.ebi.ac.uk/Tools/msa/clustalo/
Software, algorithmReliondoi:10.7554/eLife.42166
Software, algorithmCryosparcdoi:10.1038/nmeth.4169
Software, algorithmMotionCor2doi:10.1038/nmeth.4193
Software, algorithmChimeraXdoi:10.1002/pro.3943
Software, algorithmCTFFIND4doi:10.1016/j.jsb.2015.08.008

Cell culture

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HEK293T cells were purchased from ATCC, routinely maintained in the lab without further authentication, and tested negative for mycoplasma. HEK293T cells endogenously expressing PAC channel, or PAC KO HEK293T cells, generated previously using CRISPR technology (Yang et al., 2019) were maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin (P/S) at 37 °C in humidified 95% CO2 incubator. All PAC mutants mentioned in this manuscript were expressed and recorded in the PAC KO HEK2935 cell line. PAC KO cells were transfected with 500–800 ng/ml of plasmid DNA using Lipofectamine 2000 (Life Technologies according to the manufacturer’s instructions. Cells were seeded on 12 mm diameter Poly-L-lysine Sigma-Aldrich) coated glass coverslips and were recorded within 24 hr after seeding/transfection.

Constructs and mutagenesis

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Human PAC isoform 2 coding sequence (NP_060722), previously subcloned into pIRES2-EGFP vector (Clontech) using XhoI and EcoRI restriction enzyme sites (Yang et al., 2019), was used for whole-cell patch-clamp recording experiments. Zebrafish PAC coding sequence (NP_001278691) was subcloned into pIRES2-EGFP vector (Clontech) using NheI and EcoRI restriction enzyme sites. Mutations were introduced using sense and antisense oligos with 15 base pairs of homology on each side of the mutated site. Site-directed mutagenesis was carried out using QuikChange II XL site-directed mutagenesis kit (Agilent Technologies) according to the manufacturer’s instructions. All constructs were confirmed by sequencing the entire open reading frame using Sanger sequencing.

Sequence alignments

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PAC multiple protein sequence alignments were created using Clustal Omega software (EMBL-EBI). Protein sequences from the following vertebrate species were obtained from UniProt (ID): human PAC (Q9H813), rat PAC (Q66H28), mouse PAC (Q9D771), frog PAC (Q0V9Z3), zebrafish PAC (Q7SY31), bovine PAC (Q2KHV2), orangutan PAC (Q5RDP8), chicken PAC (E1C5B3), and green anole PAC (G1KFB8).

Lipids and chemicals

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All lipids used in this paper were ordered from Avanti Polar Lipids, and dissolved in water or DMSO, depending on the chain length, to make stock solutions. If not stated otherwise, lipids were added at 10 µM concentration directly to the extracellular solution. Please refer to the table for the list of all the lipids used in this paper. Poly-L-Lysine (PLL) (Sigma-Aldrich) was added to the intracellular solution at 100 μg/ml.

Electrophysiology

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Whole-cell patch-clamp experiments were performed using the extracellular recording solution (ECS) containing (in mM): 145 NaCl, 2 MgCl2, 2 KCl, 1.5 CaCl2, 10 HEPES, 10 glucose. The osmolarity of the ECS solution was 300–310 mOsm/kg and the pH was titrated to 7.3 using NaOH. Acidic extracellular solutions contained the same ionic composition, except 5 mM sodium citrate was used as a buffer instead of HEPES, and the pH was adjusted using citric acid. ECS solutions were applied 100–200 µm away from the recording cell, using a gravity perfusion system with a small tip. Recording patch pipettes, made of borosilicate glass (Sutter Instruments), were pulled with a Model P-1000 multi-step puller (Sutter Instruments). The patch pipettes had a resistance of 2–4 MΩ when filled with an intracellular solution (ICS) containing (in mM): 135 CsCl, 2 CaCl2, 1 MgCl2, 5 EGTA, 4 MgATP, 10 HEPES. The osmolarity of the ICS solution was 280–290 mOsm/kg and pH was titrated to 7.2 using CsOH. ICl, H recordings were acquired using voltage ramp pulses from –100 to + 100 mV. The time interval between two ramp pulses was 2 or 5 s at a speed of 1 mV/ms and the holding potential was 0 mV. All recordings were performed with a MultiClamp 700B amplifier and 1550B digitizer (Molecular Devices) at room temperature. Signals were filtered at 2 kHz, digitized at 10 kHz, and the series resistance was compensated for at least 80% (Yang et al., 2019).

Data analysis

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Electrophysiology data were analyzed using Clampfit 10.7. Statistical analysis was performed using GraphPad Prism 9 software. Comparison between two groups was carried out using an unpaired two-tailed Student’s t test unless stated otherwise. Multiple group comparisons were performed using ordinary one-way analysis of variance (ANOVA). The significance level was set at p<0.05. All numerical data are shown as mean ± SEM. For the time-constant experiments, the currents were fit using a one-phase decay equation: Y=(Y0 - Plateau)*exp(-K*X)+Plateau, where Y0 was the time-point of adding PIP2 to the cells. For the IC50 values, the normalized data was fitted to the following sigmoidal 4PL equation, where X is log (concentration): Span = Top - Bottom; Y=Bottom + (Top-Bottom)/(1+10^((LogIC50-X)*HillSlope)) (Ruan et al., 2020).

Protein expression and purification

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The pEGC-hPAC plasmid containing the human PAC gene, a Strep-tag II tag, a thrombin cleavage site, an eGFP, and an 8xHis tag, was used for expressing PAC protein in mammalian cells using BacMam system (Goehring et al., 2014, Ruan et al., 2020). The bacmid was produced by transforming the DH10Bac cells with pEGC-hPAC plasmid. Positive white clones were selected from a Luria Broth (LB) plate with kanamycin (50 μg/mL), tetracycline (10 μg/mL), gentamicin (7 μg/mL), Bluo-gal (100 μg/mL Bluo-gal), and IPTG (40 μg/mL). Bacmid DNA was purified from LB cultures of the white colonies using the alkaline lysis method. The bacmid was then transfected into adherent Sf9 cells grown in Sf-900 II media (Gibco) using Cellfectin II reagent by following the manufacturer’s recommended protocol. After 5 days, the media of Sf9 cell culture was filtered and stored as the P1 virus. Subsequently, the P2 virus was made by infecting suspension Sf9 cells grown in Sf-900 II media with P1 virus at a 1:5000 ratio (v/v). After 5 days, the media containing P2 virus was harvested, filtered, and stored at 4 °C with 1% fetal bovine serum (FBS). Mammalian cells (tsA-201 cell line) grown in FreeStyle 293 media (Gibco) supplemented with 1% FBS was used for protein expression. When suspension cells reached 3.5x10^6 cells/ml density, 10% (v/v) P2 virus was added to tsA-201 cells, and cells were allowed to grow for 8–12 hr at 37 °C. To boost protein expression, 5 mM sodium butyrate was added to the cell culture, and cells were allowed to grow for another 60 hr at 30 °C. The mammalian cells expressing PAC were then spun down at 6000 rpm for 15 min, and the pellet is stored at –80 °C until protein purification.

The cell pellet was resuspended in ice-cold TBS buffer (20 mM Tris pH 8 and 150 mM NaCl) with a protease inhibitor cocktail (1  mM PMSF, 0.8  μM aprotinin, 2  μg/ml leupeptin, 2  mM pepstatin A) and lysed by sonication. The debris was removed by centrifugation at 4000 rpm for 10 min at 4 °C. The supernatant underwent ultracentrifugation at 40,000 rpm for 1 hr and the cell membrane was collected. The membrane was solubilized in TBS buffer with 1% glyco-diosgenin (GDN) detergent (Anatrace) and the protease inhibitor cocktail for 1 hr at 4 °C with gentle rotation. The sample was clarified by ultracentrifugation at 40,000 rpm for 1 hr. The supernatant was subjected to immobilized metal affinity chromatography (IMAC) with talon resin (Takara Bio USA). The bound protein was washed with TBS buffer containing 0.02% GDN and 20 mM imidazole and eluted with TBS buffer containing 0.02% GDN and 250 mM imidazole. The PAC protein was then concentrated to 1 ml using a 100 kDa concentrator. The sample was then mixed with soybean lipid extract (Anatrace) and His-tag free membrane scaffold protein 1E3D1 (Denisov et al., 2007) at a 1:200:3 molar ratio. The GDN detergent was removed through three rounds of biobeads (Bio-Rad) incubation at 4 °C. To remove ‘empty’ nanodiscs, the sample was filtered to remove biobeads and incubated with talon resin at 4 °C for another 1 hr. The volume of the sample was expanded to 25 ml by adding TBS buffer such that the imidazole concentration was at 10 mM. The resin was washed with TBS buffer containing 10 mM imidazole, and the protein was eluted with TBS buffer containing 250 mM imidazole. PAC-nanodisc protein was then concentrated to 500 μL using an Amicon Ultra-15 concentrator (100 kDa cutoff). Thrombin (0.03 mg/ml) was added to cleave GFP from the PAC protein at 4 °C overnight. PAC-nanodisc was further purified by size-exclusion chromatography (SEC) using TBS buffer. The peak fractions were concentrated to 5 mg/ml before making cryo-EM grids.

Cryo-EM grid preparation

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Purified human PAC protein in nanodiscs was first mixed with 1 mM diC8-PI(4,5)P2 (Avanti) on ice for 1 hr. The pH of the protein sample was adjusted to 4.0 by adding an acidic acid buffer (1 M, pH 3.5) at a 1:20 ratio (v/v). We also added 0.5 mM fluorinated octyl maltoside (Anatrace) to improve sample quality. An FEI Vitrobot Mark III was used for plunge-freezing. Specifically, a 3 μl aliquot of the protein sample was applied to a glow-discharged Quantifoil holey carbon grid (Au 300 2/1 mesh) (Electron Microscopy Sciences), blotted for 2 s, vitrified in liquid ethane, and transferred to liquid nitrogen for storage. The temperature and humidity of the chamber was kept at 18 °C and 100% throughout the grid preparation.

Cryo-EM data collection

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The cryo-EM grids were initially screened in an FEI Talos Arctica transmission electron microscope equipped with a K2 summit camera. High-resolution data collection was facilitated by the Pacific Northwest Center for Cryo-EM (PNCC) using an FEI Titan Krios transmission electron microscope equipped with a BioQuantum energy filter (20 eV slit width) and a K3 camera with a nominal magnification of 105,000. SerialEM was used for automated data collection in super-resolution mode with a pixel size of 0.413 Å (Mastronarde, 2005). The raw movie stack contained a total of 52 frames with a total dose of 50 e–/Å2. The nominal defocus value was allowed to vary between –0.6 and –2.4 μ m.

Cryo-EM data processing

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The cryo-EM data processing workflow is summarized in Figure 3—figure supplement 2. Specifically, the raw movies were motion corrected using relion 3.1 and binned to the physical pixel size at 0.826 Å (Zivanov et al., 2018). The defocus parameters of motion-corrected micrographs were estimated using ctffind 4.1.10 (Rohou and Grigorieff, 2015). Particle picking was performed using both gautomatch_v0.56 and topaz v0.2.5 (Bepler et al., 2019). Particles picked by each program were independently subjected to 2D classification (relion 3.1) or heterogeneous refinement with C1 symmetry (cryosparc v3.0) to get rid of junk particles (Punjani et al., 2017; Zivanov et al., 2018). Good particles with clear features were pooled together and refined in relion 3.1. 3D refinement with a solvent mask and C3 symmetry, resulting in a 4.4 Å map. We noticed that the size of nanodiscs could be heterogeneous, which may negatively affect particle alignment. Therefore, we created a loose mask of the protein based on the atomic model and performed signal subtraction to remove the nanodisc signal. The process allowed us to obtain a reconstruction at 4.2 Å resolution. To sort out the conformational heterogeneity of the dataset, we performed 3D classification without image alignment in relion 3.1. The best class of the job was selected and refined to 3.6 Å resolution. We then performed several rounds of CTF refinement and Bayesian polishing (Zivanov et al., 2019), and the map was eventually refined to 3.17 Å. We noticed an improvement in the map quality when the box size of the images was expanded from 240 pixels to 300 pixels at this stage. To further improve map reconstruction, we first split the original consensus particles after 2D and heterogeneous refinement into 6 portions. We combined each portion with the best particles that gave rise to the 3.17 Å reconstruction and performed another round of 3D classification. This procedure was effective in attracting good particles from the initial consensus map particles. After combining the best class and removing duplicates, we identified 84 k particles that could be refined to 3.07 Å in relion after iterative CTF refinement and Bayesian Polishing. We then exported the particles to cryosparc and conducted CTF refinement followed by local refinement. We also supplied a mask to get rid of nanodisc signal during the refinement. In the end, we obtained a 2.71 Å reconstruction as judged by gold-standard Fourier shell correlation. This map is deposited in the EMDB under the accession EMD-28535. We noticed that the intracellular side of TMD is very heterogeneous, which may limit the quality of the final reconstruction. As the last step of our data analysis, we refined the particles by using a mask that excludes signals of the intracellular region of PAC. This additional step allowed us to obtain a reconstruction of PAC ECD and the extracellular region of TMD at 2.70 Å (Figure 3—figure supplement 2). Although the nominal resolution of this map is comparable to the full protein map, we noticed improved map quality, especially the lipid density. Postprocessing of the maps, including local map sharpening and resolution estimation is performed using Phenix (Terwilliger et al., 2018). This map is deposited in the EMDB under the accession EMD-28964.

Model building, validation, and analysis

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The atomic model was generated by first docking the structural model of human PAC at pH 4.5 (PDBID: 7SQH) into the cryo-EM map (Wang et al., 2022). The diC8-PI(4,5)P2 molecule was manually placed into the cryo-EM density. The Grade Web Server (Bepler et al., 2019) was used to generate a restraint file for flexible fitting of the diC8-PI(4,5)P2 molecule. Subsequently, the model underwent real space refinement in phenix and manual adjustment to fix Ramachandran outliers, rotamer outliers, and clashes (Adams et al., 2010). We manually removed the phosphatidylinositol 4,5-bisphosphate group from the atomic model due to the limited support from the cryo-EM density. The final model was validated by the molprobity in phenix to obtain validation statistics (Williams et al., 2018). The cryo-EM map and atomic model were visualized using UCSF ChimeraX (Pettersen et al., 2021). The pore profile of the PAC channel was calculated using the HOLE 2.0 program (Smart et al., 1996).

Data availability

The cryo-EM density maps have been deposited in the EMDB (Electron Microscopy Data Bank) under accession numbers EMD-28535 and EMD-28964. The atomic models have been deposited in the Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCS-PDB) under accession numbers 8EQ4 and 8FBL.

The following data sets were generated
    1. Mihaljevic L
    2. Ruan Z
    3. Osei-Owusu J
    4. Lu W
    5. Qiu Z
    (2022) Electron Microscopy Data Bank
    ID EMD-28535. Cryo-EM structure of PAC channel with PIP2.
    https://www.ebi.ac.uk/emdb/EMD-28535
    1. Mihaljevic L
    2. Ruan Z
    3. Osei-Owusu J
    4. Lu W
    5. Qiu Z
    (2022) Electron Microscopy Data Bank
    ID EMD-28964. Cryo-EM structure of PAC channel with PIP2.
    https://www.ebi.ac.uk/emdb/EMD-28964
    1. Mihaljevic L
    2. Ruan Z
    3. Osei-Owusu J
    4. Lu W
    5. Qiu Z
    (2022) RCSB Protein Data Bank
    ID 8EQ4. Cryo-EM structure of PAC channel with PIP2.
    https://www.rcsb.org/structure/8EQ4
    1. Mihaljevic L
    2. Ruan Z
    3. Osei-Owusu J
    4. Lu W
    5. Qiu Z
    (2022) RCSB Protein Data Bank
    ID 8FBL. Cryo-EM structure of PAC channel with PIP2.
    https://www.rcsb.org/structure/8FBL

References

Decision letter

  1. Andrés Jara-Oseguera
    Reviewing Editor; The University of Texas at Austin, United States
  2. Richard W Aldrich
    Senior Editor; The University of Texas at Austin, United States
  3. Andrés Jara-Oseguera
    Reviewer; The University of Texas at Austin, United States
  4. Valeria Kalienkova
    Reviewer; University of Groningen, Netherlands

Our editorial process produces two outputs: (i) public reviews designed to be posted alongside the preprint for the benefit of readers; (ii) feedback on the manuscript for the authors, including requests for revisions, shown below. We also include an acceptance summary that explains what the editors found interesting or important about the work.

Decision letter after peer review:

Thank you for submitting your article "Inhibition of the proton-activated chloride channel PAC by PIP2" for consideration by eLife. Your article has been reviewed by 3 peer reviewers, including Andrés Jara-Oseguera as Reviewing Editor and Reviewer #1, and the evaluation has been overseen by Richard Aldrich as the Senior Editor. The following individual involved in the review of your submission has agreed to reveal their identity: Valeria Kalienkova (Reviewer #2).

The reviewers have discussed their reviews with one another, and the Reviewing Editor has drafted this to help you prepare a revised submission. All three reviewers agreed that the findings in the manuscript are interesting and important, but they also raised a series of concerns, the two major ones concerning whether the inhibition of PAC channels by PIP2 is physiologically relevant, and whether the lipid bound to the channel in the structure is indeed PIP2. Each of the concerns discussed by the reviewers are summarized below.

Essential revisions:

1. Since the authors show that PIP2 rather acts on an activated/desensitized state of the channel, the authors should discuss the state of the PIP2 binding site in different states of the channel – resting, activated and desensitized. Is it unavailable to PIP2 in resting state? Related to this, do previously solved desensitized structures have any defined lipid densities in that region? If this is not the case, this might be worth mentioning to further strengthen the point that the density observed in this new structure might indeed be a specifically-bound PIP2 molecule.

2. For Figure 3C (PIP2 binding site), please include the cryo-EM density for the lipid, the fitted PIP2 molecule, and the density for the side-chains that are interacting with the lipid. The experimental evidence identifying PIP2 as the bound lipid should be discussed more extensively, and it should be clearly acknowledged in the paper if there are alternative explanations for the observations: does the density uniquely identify the lipid as PIP2, or could other lipids be fitted, including potential lipid contaminants such as phosphatidic acid? The authors need to clarify whether their experimentally resolved data supports the positioning of bound PIP2 in the PAC structure (Figure 3A-C) or does not (the main text and figure legends, Figure S4).

Please also clarify if the longer acyl chains are proposed to contribute to tighter binding of the lipid and orientation of the headgroup into the pocket. This is important because the headgroup does not seem to bind very tightly and is hence not very well resolved. Is the pocket big enough to accommodate PIP3? Does the higher number of phosphates simply help to attract the headgroup towards this pocket? Finally, note the pKA of inositol phosphates (Kooijman et al. 2009, PMID: 19725516); they will be partially protonated at pH 4.

3. The authors need to address the subcellular localization of PI(4,5)P2 and why their findings are surprising. Although they cite previous studies that have identified PI(4,5)P2 on the outer leaflet of the plasma membrane, it is a minor component of total PIP2 (see Yoneda et al. 2020, Figure 1). The localization and function of cellular PIP2 has been extensively studied (reviewed in Schink et al. 2016, PMID 27576122) and few roles for extracellular/lumenal PIP2 have been described to date. It is unlikely (albeit possible) that a native regulatory mechanism for PIP2 exists in this context, and the conclusions of the paper should reflect this fact.

4. While the unsharpened map looks symmetric, the sharpened one does not – what is the reason for this discrepancy? Please indicate in Materials and methods if C3 symmetry was applied throughout the refinement for the 4.2 A map. The authors might consider trying other sharpening tools which take into account different b-factors across the map (deepEMhancer, local deblur, sharpening tools in Phenix etc). Please include the reasoning for the final mask excluding part of the transport domain in data processing section of Materials and methods, and display the mask in the processing workflow in figure S3. Regarding figure S3, please indicate what is displayed in color, and what are the transparent outlines – are those depictions of the maps at different contour? Or are the transparent outlines masks used for sharpening? If it is the latter, the final mask also includes nanodisc density.

5. Application of PIP2 in Figure 4A-C produces an immediate drop of current that appears independent from the decay curves ascribed to desensitization. The brackets on those figures indicate that inhibition was measured 75-100 seconds after application, thus incorporating a mix of both processes. This measurement needs to be consistent across experiments and should be explained more clearly. Also, the rate of desensitization before and after PIP2 does not seem to change after the rapid current decay upon first exposure to PIP2 – this seems inconsistent with the proposed mechanism of inhibition by PIP2 in which the lipid increases the rate of desensitization. Please show the fits for the one-phase decay equations. The drop of current visible after PIP2 application suggests that such a model is inappropriate. These discrepancies need to be appropriately addressed. In the discussion, "PIP2 could only slowly shift the equilibrium toward the desensitized state" is not supported by the data in Figure 4.

6. Experiments with the PAC KO cell line should be included showing that the increase in current caused by low pH, and its inhibition by applied PIP2 are only observed in cells that were transfected with WT PAC channels.

7. It must be clarified whether the PAC KO cell line was used for all experiments with mutants.

8. Table S1, map resolution range: is 246 A a typo? This seems unusually low.

9. Although not necessary, it would strengthen the manuscript if measurements of the desensitization rate for key mutants in Figure 3E were included.

10. In the introduction, a citation is needed for the statement "TMEM16A is known to require PIP2 for channel opening."

11. No significant difference is reported between the IC50 of PIP2 and PIP3. The text "the additional phosphate on PIP3 further lowered the IC50…" is not supported by the data.

12. In Figure 2(D), diC18:1-PI(4,5)P2 is incorrectly described as natural.

13. Also in Figure 2(D), poor solubility is used to justify using diC18:1-PI(4,5)P2 at higher concentration. This doesn't make sense; higher concentrations reduce solubility. The authors should consider addressing this discrepancy.

14. In the discussion, "the desensitized conformation becomes more prevalent and accessible" should be changed to reflect that the binding site becomes more accessible.

15. In the discussion, ABCA1 is proposed as a shuttle for PIP2 in cells expressing PAC channels. Do these proteins co-express?

16. The manuscript states that PAC/ASOR is the first Cl- channel to be inhibited by PIP2. TMEM16B is inhibited by PIP2, reported first in the following manuscript: Ta et al. 2017, PMID 28616863.

17. Please review the methods section for grammar and capitalization errors.

Reviewer #1 (Recommendations for the authors):

1) Experiments with the PAC KO cell line should be included showing that the increase in current caused by low pH, and its inhibition by applied PIP2 are only observed in cells that were transfected with WT PAC channels.

2) It must be clarified whether the PAC KO cell line was used for all experiments with mutants.

3) Including measurements of the desensitization rate for key mutants included in Figure 3E would strengthen the conclusions for a direct interaction between PIP2 and the proposed site on the channel.

4) A more critical discussion should be included that examines what other types of lipids could be occupying the density that is assigned to PIP2 in the study.

Reviewer #2 (Recommendations for the authors):

1. Since the authors show that PIP2 rather acts on an activated/desensitized state of the channel, it would be interesting to show the PIP2 binding site in different states of the channel – resting, activated and desensitized. Is it unavailable to PIP2 in resting state? Related to this, do previously solved desensitized structures have any defined lipid densities in that region? If this is not the case, this might be worth mentioning to further strengthen the point that the density observed in this new structure might indeed be a specifically-bound PIP2 molecule.

2. Description of the PIP2-binding site, page 7 bottom line: this could benefit from figure with a close-up of PIP2 binding site, with the corresponding cryo-EM density, and the fitted PIP2 molecule. Page 8, end of the first paragraph, I feel the explanation could be expanded further: do the longer acyl chains help tighter binding of the lipid and orientation of the headgroup into the pocket? Is this important because the headgroup does not bind very tightly and is hence not very well resolved? Is the pocket big enough to accommodate PIP3? Does the higher number of phosphates simply help to attract the headgroup towards this pocket?

3. While the unsharpened map looks symmetric, the sharpened one does not, what is the reason for this discrepancy? Perhaps also worth indicating in Materials and methods if from the point of 3D refinement which gave the 4.2 A map C3 symmetry was applied throughout. The authors might consider trying other sharpening tools which take into account different b-factors across the map (deepEMhancer, local deblur, sharpening tools in Phenix etc). It would also be valuable to include the reasoning for the final mask excluding part of the transport domain in data processing section of Materials and methods, and to display the mask in the processing workflow in figure S3. Regarding figure S3, please indicate what is displayed in color, and what are the transparent outlines – are those depictions of the maps at different contour? Or are the transparent outlines masks used for sharpening? If it is the latter, the final mask also includes nanodisc density, contrary to

4. While not absolutely necessary, it could be helpful to mention for those unfamiliar with this protein family that it is also referred to as ASOR.

5. Table S1, map resolution range: is 246 A a typo? This seems unusually low.

Reviewer #3 (Recommendations for the authors):

1) The authors need to address the subcellular localization of PI(4,5)P2 and why their findings are surprising. Although they cite previous studies that have identified PI(4,5)P2 on the outer leaflet of the plasma membrane, it is a minor component of total PIP2 (see Yoneda et al. 2020, Figure 1). The localization and function of cellular PIP2 has been extensively studied (reviewed in Schink et al. 2016, PMID 27576122) and few roles for extracellular/lumenal PIP2 have been described to date. It is unlikely (albeit possible) that a native regulatory mechanism for PIP2 exists in this context, and the conclusions of the paper should reflect this fact.

2) The density of PAC with PIP2 (Figure S4) does not support the placement of the PIP2 headgroup. The authors acknowledge this fact with the following points in the Results section: "it is by no means unambiguous due to the limited local map resolution" and "the phosphatidyl group is reasonably well defined… in contrast, the inositol 4,5-bisphosphate moiety is not resolved". Confusingly, the authors also state that the deposited model does not contain the inositol headgroup (Figure 3A) but the attached validation files indicate that it has been (Molecule 3, PIO "Ligand of interest"). The authors need to decide whether their experimentally resolved data supports the positioning of bound PIP2 in the PAC structure (Figure 3A-C) or does not (the main text and figure legends, Figure S4). In doing so, the authors should consider the possibility of contaminating ligands from the other lipids (e.g. phosphatidic acid) in their preparation. Furthermore, in absence of supporting data, Figure 3C should be excluded from the manuscript. While it is apparent that the modeled basic residues are important for PAC inhibition by PIP2 (Figure 3E) and the authors are careful to note that the model is used to highlight the local biochemical (electrostatic) environment, the presentation of the figure (e.g. distance lines for electrostatic interactions) suggests more certainty than is warranted. Finally, note the pKA of inositol phosphates (Kooijman et al. 2009, PMID: 19725516); they will be partially protonated at pH 4.

https://doi.org/10.7554/eLife.83935.sa1

Author response

Essential revisions:

1. Since the authors show that PIP2 rather acts on an activated/desensitized state of the channel, the authors should discuss the state of the PIP2 binding site in different states of the channel – resting, activated and desensitized. Is it unavailable to PIP2 in resting state? Related to this, do previously solved desensitized structures have any defined lipid densities in that region? If this is not the case, this might be worth mentioning to further strengthen the point that the density observed in this new structure might indeed be a specifically-bound PIP2 molecule.

The residues that form the PIP2 binding site are part of the structural region that shows major conformational differences between the desensitized state and the resting/activated states (Figure S5). In particular, the rotational movement of TM1 annihilates the PIP2 binding pocket in the resting and activated states of PAC (Figure S5). Therefore, it’s unlikely that PIP2 binds to PAC in these states. We thank the reviewer for raising such a good point and we now generate a new figure to further demonstrate this point (Figure S5).

Our previous structure in the desensitized state doesn't contain such a lipid density (Ruan et al., Nature, 2020). The recent high-resolution structure of PAC appears to contain a branched lipid density in the area in two of the subunits but not the third one. We are unsure about the reason as the map is supposed to be refined using C3 symmetry. The map deposited in the EMDB (EMD-25385) looks distorted and doesn’t appear to be a raw cryo-EM map generated directly by gold-standard 3D refinement. We are unsure how to best interpret the map (Wang et al., Sci Adv, 2022). Therefore, we decide not to discuss this part in our manuscript.

2. For Figure 3C (PIP2 binding site), please include the cryo-EM density for the lipid, the fitted PIP2 molecule, and the density for the side-chains that are interacting with the lipid. The experimental evidence identifying PIP2 as the bound lipid should be discussed more extensively, and it should be clearly acknowledged in the paper if there are alternative explanations for the observations: does the density uniquely identify the lipid as PIP2, or could other lipids be fitted, including potential lipid contaminants such as phosphatidic acid? The authors need to clarify whether their experimentally resolved data supports the positioning of bound PIP2 in the PAC structure (Figure 3A-C) or does not (the main text and figure legends, Figure S4).

Please also clarify if the longer acyl chains are proposed to contribute to tighter binding of the lipid and orientation of the headgroup into the pocket. This is important because the headgroup does not seem to bind very tightly and is hence not very well resolved. Is the pocket big enough to accommodate PIP3? Does the higher number of phosphates simply help to attract the headgroup towards this pocket? Finally, note the pKA of inositol phosphates (Kooijman et al. 2009, PMID: 19725516); they will be partially protonated at pH 4.

We have revised Figure 3C to show the density of the lipid and important residues nearby. We also mentioned the possibilities of other lipids in the text. In our initial manuscript, we already acknowledged the fact that the assignment of PIP2 into the density is not unambiguous based on the cryo-EM map alone. However, the biochemical environment of the binding pocket, as well as the subsequent mutagenesis data support such a PIP2 binding site. We now re-wrote the paragraph to make this even clearer.

We propose that lipid chain of at least 8 carbons is necessary for PAC inhibition due to insertion into the membrane, which potentially makes the PIP2 headgroup accessible to the positively charged pocket on PAC. Lipid with a shorter chain, diC6-PIP2, didn’t inhibit PAC and the lipid with a chain longer than 8 carbons, diC18:0-20:4-PIP2, didn’t further increase the inhibition (when compared to diC8-PIP2), suggesting that C7 and C8 carbon of the acyl chain establish critical interactions with the protein. Additionally, our structural model showed that the acyl chain of PIP2 tightly packs against W304. The importance of the acyl chain for PIP2 binding is supported by the fact that the W304A mutant resulted in reduced PIP2 inhibition (Figure 3E).

The binding pocket is big enough to accommodate PIP3. In fact, we can place a phosphate group at the 3rd position of the inositol hydroxyl group in our current PDB model without creating any steric hindrance. Because the electrostatic environment surrounding the headgroup of PIP2 is positively charged (Figure 3C), we believe the attraction effect is a major factor that contributes to the recognition of PIP2.

We acknowledge the referenced literature (Kooijman et al. 2009, PMID: 19725516) that the phosphate group may be partially protonated at pH 4, but this study is unable to reliably estimate the pKa2 of PI(4,5)P2 and the pKa1 is not studied. Moreover, in Figure 7 of the paper, no major difference is observed in the charge status of PI(4,5)P2 at pH 4-5, suggesting that the ionization status of PIP2 doesn’t change in the experimental condition investigated in our study. In a more recent review of PI(4,5)P2, it was suggested that at pH 4-5, both of the phosphomonoester groups are mono-protonated (Luís Borges-Araújo and Fabio Fernandes 2020, PMID: 32858905). Therefore, a net charge of -2 is present in the head group of PI(4,5)P2 under our experimental conditions, which allowed the molecule to interact favorably with the positively charged binding pocket (Figure 3C).

3. The authors need to address the subcellular localization of PI(4,5)P2 and why their findings are surprising. Although they cite previous studies that have identified PI(4,5)P2 on the outer leaflet of the plasma membrane, it is a minor component of total PIP2 (see Yoneda et al. 2020, Figure 1). The localization and function of cellular PIP2 has been extensively studied (reviewed in Schink et al. 2016, PMID 27576122) and few roles for extracellular/lumenal PIP2 have been described to date. It is unlikely (albeit possible) that a native regulatory mechanism for PIP2 exists in this context, and the conclusions of the paper should reflect this fact.

Thank you for this insight, we agree that PIP2 predominantly localizes to the inner leaflets of the cell membrane. We have further clarified in the Discussion section of our paper that the physiological relevance (if any exists) of PIP2 inhibition of the PAC channel is unclear. Nevertheless, the novel lipid-binding pocket is a relevant discovery that can be exploited for targeted inhibition of the PAC channel.

4. While the unsharpened map looks symmetric, the sharpened one does not – what is the reason for this discrepancy? Please indicate in Materials and methods if C3 symmetry was applied throughout the refinement for the 4.2 A map. The authors might consider trying other sharpening tools which take into account different b-factors across the map (deepEMhancer, local deblur, sharpening tools in Phenix etc). Please include the reasoning for the final mask excluding part of the transport domain in data processing section of Materials and methods, and display the mask in the processing workflow in figure S3. Regarding figure S3, please indicate what is displayed in color, and what are the transparent outlines – are those depictions of the maps at different contour? Or are the transparent outlines masks used for sharpening? If it is the latter, the final mask also includes nanodisc density.

We thank the reviewer for pointing this out. We now carefully performed local anisotropic sharpening in Phenix and ensured that the output is symmetric. We also tried the deepEMhancer and local deblur. Upon visual inspection of the output, we found that the map produced by Phenix showed the best features in terms of the residue side chain and lipid density. Therefore, we deposit the Phenix map in EMDB.

We did apply C3 symmetry to obtain the initial 4.2 Å map. This is now clearly indicated in the Materials and methods.

Our final data processing procedure includes a step to exclude part of the map by using a mask. This is because substantial heterogeneity is present in the intracellular side of the transmembrane domain,. As we are primarily interested in the PIP2 binding site, which is located in the ECD-TMD interface, we decide to exclude signals in the intracellular region of the transmembrane domain for final refinement. This will allow us to improve the density for the PIP2 binding site and facilitate model building. We deposited this reconstruction as well as the full PAC map without using such a mask in EMDB in this revision.

The transparent outline is a non-sharpened map at a low contour level with the aim to show the nanodisc density. This will allow the readers to distinguish different regions of the PAC structure (ECD and TMD) easily. It is not a mask for refinement. We modified the figure S3 legend to better describe this. As the reviewer suggested, we also showed the mask used in the last step of refinement in Figure S3. This mask excluded the intracellular portion of PAC TMD.

5. Application of PIP2 in Figure 4A-C produces an immediate drop of current that appears independent from the decay curves ascribed to desensitization. The brackets on those figures indicate that inhibition was measured 75-100 seconds after application, thus incorporating a mix of both processes. This measurement needs to be consistent across experiments and should be explained more clearly. Also, the rate of desensitization before and after PIP2 does not seem to change after the rapid current decay upon first exposure to PIP2 – this seems inconsistent with the proposed mechanism of inhibition by PIP2 in which the lipid increases the rate of desensitization. Please show the fits for the one-phase decay equations. The drop of current visible after PIP2 application suggests that such a model is inappropriate. These discrepancies need to be appropriately addressed. In the discussion, "PIP2 could only slowly shift the equilibrium toward the desensitized state" is not supported by the data in Figure 4.

The reviewer raises a good point. Although the immediate drop in current is a consequence of recording resolution (5s/sweep), we have concluded that using one or two-phase decay equations are indeed not appropriate models to fit the PAC inhibition kinetics by PIP2. We, therefore, decided to exclude the kinetics from the manuscript and revised our proposed model appropriately. Furthermore, we wanted to clarify that the inhibition has been consistently quantified at 100s point after the application of PIP2, even though the start of PIP2 application had a variable time-point due to variability in desensitization current reaching a plateau. This is now clarified in the text.

6. Experiments with the PAC KO cell line should be included showing that the increase in current caused by low pH, and its inhibition by applied PIP2 are only observed in cells that were transfected with WT PAC channels.

We are thankful to the reviewer for pointing this out, however, we and others have shown repeatedly (Yang et al., 2019; PMID: 31023925, Osei-Owusu et al., 2022 PMID: 35878032; Osei-Owusu et al., 2021 PMID: 33503418; Ullrich et al., 2019; PMID: 31318332) that the chloride current elicited by low pH is absent in the PAC KO cells. In other words, there is no acid-induced chloride current (hence no current to be inhibited by PIP2) to be observed in PAC KO cells. Therefore, the currents recorded in this manuscript are PAC-specific and we believe that additional experiments are not necessary.

7. It must be clarified whether the PAC KO cell line was used for all experiments with mutants.

Thank you for this comment, we clarified further in the Materials and methods of our manuscript that all PAC mutants in the manuscript have been expressed and recorded in the PAC KO HEK293T cell line we reported previously.

8. Table S1, map resolution range: is 246 A a typo? This seems unusually low.

We thank the reviewers for pointing this out. This is indeed a typo and we have fixed this in Table S1.

9. Although not necessary, it would strengthen the manuscript if measurements of the desensitization rate for key mutants in Figure 3E were included.

Reviewer raised a good point. We quantified the amount of desensitization between the WT and the mutants at pH 5.0 (which showed no significant difference) and included it in the supplementary Figure 2F.

10. In the introduction, a citation is needed for the statement "TMEM16A is known to require PIP2 for channel opening."

We are thankful to the reviewer for this remark, we changed this sentence to include the new literature and added the appropriate citations.

11. No significant difference is reported between the IC50 of PIP2 and PIP3. The text "the additional phosphate on PIP3 further lowered the IC50…" is not supported by the data.

Thank you for pointing this out, we have made the following change: "The additional phosphate on PIP3 yielded the IC50 of 3μM " as supported by the data in the Figure 2B.

12. In Figure 2(D), diC18:1-PI(4,5)P2 is incorrectly described as natural.

Thank you for raising this point. We used a full-length diC18:0-20:0-PI(4,5)P2 instead.

13. Also in Figure 2(D), poor solubility is used to justify using diC18:1-PI(4,5)P2 at higher concentration. This doesn't make sense; higher concentrations reduce solubility. The authors should consider addressing this discrepancy.

We agree with the reviewer and we have addressed this discrepancy by performing a new experiment with 10M diC18:0-20:0-PI(4,5)P2. We have found that at this concentration full-length PIP2 potently inhibits the PAC channel.

14. In the discussion, "the desensitized conformation becomes more prevalent and accessible" should be changed to reflect that the binding site becomes more accessible.

Thank you for this comment, we have made the appropriate change in the discussion to reflect this.

15. In the discussion, ABCA1 is proposed as a shuttle for PIP2 in cells expressing PAC channels. Do these proteins co-express?

We are thankful to the reviewer for raising this point. PAC shows a broad expression across different tissues (Yang et al., 2019; PMID: 31023925; Ullrich et al., 2019; PMID: 31318332) and so does ABCA1 (Fagerberg et al., 2014; PMID 24309898), therefore the coincidence of co-expression between these two proteins is high.

16. The manuscript states that PAC/ASOR is the first Cl- channel to be inhibited by PIP2. TMEM16B is inhibited by PIP2, reported first in the following manuscript: Ta et al. 2017, PMID 28616863.

We are thankful to the reviewer for this insight, and we have made the changes in our manuscript to reflect this literature.

17. Please review the methods section for grammar and capitalization errors.

We have addressed this.

Reviewer #1 (Recommendations for the authors):

1) Experiments with the PAC KO cell line should be included showing that the increase in current caused by low pH, and its inhibition by applied PIP2 are only observed in cells that were transfected with WT PAC channels.

We are thankful to the reviewer for pointing this out, however, we and others have shown repeatedly (Yang et al., 2019; PMID: 31023925, Osei-Owusu et al., 2022 PMID: 35878032; Osei-Owusu et al., 2021 PMID: 33503418; Ullrich et al., 2019; PMID: 31318332) that the current elicited by low pH is absent in the PAC KO cells. In other words, there is no acid-induced chloride current (hence no current to be inhibited by PIP2) to be observed in PAC KO cells. Therefore, the currents recorded in this manuscript are PAC-specific and we believe that additional experiments are not necessary.

2) It must be clarified whether the PAC KO cell line was used for all experiments with mutants.

Thank you for this comment, we clarified further in the Materials and methods of our manuscript that all PAC mutants in the manuscript have been expressed and recorded in the PAC KO HEK293T cell line we reported previously.

3) Including measurements of the desensitization rate for key mutants included in Figure 3E would strengthen the conclusions for a direct interaction between PIP2 and the proposed site on the channel.

Reviewer raised a good point. We quantified the amount of desensitization between the WT and the mutants at pH 5.0 (which showed no significant difference) and included it in the supplementary Figure 2F.

4) A more critical discussion should be included that examines what other types of lipids could be occupying the density that is assigned to PIP2 in the study.

We are grateful to the reviewer for making this point. We of course cannot completely exclude the possibility that this density may represent other types of lipids, such as phosphatidic acid. We have now specifically mentioned this in the text.

Reviewer #2 (Recommendations for the authors):

1. Since the authors show that PIP2 rather acts on an activated/desensitized state of the channel, it would be interesting to show the PIP2 binding site in different states of the channel – resting, activated and desensitized. Is it unavailable to PIP2 in resting state? Related to this, do previously solved desensitized structures have any defined lipid densities in that region? If this is not the case, this might be worth mentioning to further strengthen the point that the density observed in this new structure might indeed be a specifically-bound PIP2 molecule.

The residues that form the PIP2 binding site are part of the structural region that shows major conformational differences between the desensitized state and the resting/activated states (Figure S5). In particular, the rotational movement of TM1 annihilates the PIP2 binding pocket in the resting and activated states of PAC (Figure S5). Therefore, it’s unlikely that PIP2 binds to PAC in these states. We thank the reviewer for raising such a good point and we now generate a new figure to further demonstrate this point (Figure S5).

Our previous structure in the desensitized state doesn't contain such a lipid density (Ruan et al., Nature, 2020). The recent high-resolution structure of PAC appears to contain a branched lipid density in the area in two of the subunits but not the third one. We are unsure about the reason as the map is supposed to be refined using C3 symmetry. The map deposited in the EMDB (EMD-25385) looks distorted and doesn’t appear to be a raw cryo-EM map generated directly by gold-standard 3D refinement. We are unsure how to best interpret the map (Wang et al., Sci Adv, 2022). Therefore, we decide not to discuss this part in our manuscript.

2. Description of the PIP2-binding site, page 7 bottom line: this could benefit from figure with a close-up of PIP2 binding site, with the corresponding cryo-EM density, and the fitted PIP2 molecule. Page 8, end of the first paragraph, I feel the explanation could be expanded further: do the longer acyl chains help tighter binding of the lipid and orientation of the headgroup into the pocket? Is this important because the headgroup does not bind very tightly and is hence not very well resolved? Is the pocket big enough to accommodate PIP3? Does the higher number of phosphates simply help to attract the headgroup towards this pocket?

We have revised Figure 3C to show the density of the lipid and important residues nearby. In our initial manuscript, we already acknowledged the fact that the assignment of PIP2 into the density is not unambiguous based on the cryo-EM map. However, the biochemical environment of the binding pocket, as well as the subsequent mutagenesis data support such a PIP2 binding site. We now re-wrote the paragraph to make this even clearer.

We propose that lipid chain of at least 8 carbons is necessary for PAC inhibition due to insertion into the membrane, which potentially makes the PIP2 headgroup accessible to the positively charged pocket on PAC. Lipid with a shorter chain, diC6-PIP2, didn’t inhibit PAC and the lipid with a chain longer than 8 carbons, diC18:0-20:4-PIP2, didn’t further increase the inhibition (when compared to diC8-PIP2), suggesting that C7 and C8 carbon of the acyl chain establish critical interactions with the protein. Additionally, our structural model showed that the acyl chain of PIP2 tightly packs again W304. The importance of the acyl chain for PIP2 binding is supported by the fact that the W304A mutant resulted in reduced PIP2 inhibition.

The binding pocket is big enough to accommodate PIP3. In fact, we can place a phosphate group at the 3rd position of the inositol hydroxyl group in our current PDB model without creating any steric hindrance. Because the electrostatic environment surrounding the headgroup of PIP2 is positively charged (Figure 3C), we believe the attraction effect is a major factor that contributes to the recognition of PIP2.

3. While the unsharpened map looks symmetric, the sharpened one does not, what is the reason for this discrepancy? Perhaps also worth indicating in Materials and methods if from the point of 3D refinement which gave the 4.2 A map C3 symmetry was applied throughout. The authors might consider trying other sharpening tools which take into account different b-factors across the map (deepEMhancer, local deblur, sharpening tools in Phenix etc). It would also be valuable to include the reasoning for the final mask excluding part of the transport domain in data processing section of Materials and methods, and to display the mask in the processing workflow in figure S3. Regarding figure S3, please indicate what is displayed in color, and what are the transparent outlines – are those depictions of the maps at different contour? Or are the transparent outlines masks used for sharpening? If it is the latter, the final mask also includes nanodisc density, contrary to

We thank the reviewer for pointing this out. We now carefully performed local anisotropic sharpening in Phenix and ensured that the output is symmetric. We also tried the deepEMhancer and local deblur. Upon visual inspection of the output, we found that the map produced by Phenix showed the best features in terms of the residue side chain and lipid density. Therefore, we deposit the Phenix map in EMDB.

We did apply C3 symmetry to obtain the initial 4.2 Å map. This is now clearly indicated in the Materials and methods.

Our final data processing procedure includes a step to exclude part of the map by using a mask. This is because substantial heterogeneity is present in the intracellular side of the transmembrane domain,. As we are primarily interested in the PIP2 binding site, which is located in the ECD-TMD interface., we decide to exclude signals in the intracellular region of the transmembrane domain for final refinement. This will allow us to improve the density for the PIP2 binding site and facilitate model building. We deposited this reconstruction as well as the full PAC map without using such a mask in EMDB in this revision.

The transparent outline is a non-sharpened map at a low contour level with the aim to show the nanodisc density. This will allow the readers to distinguish different regions of the PAC structure (ECD and TMD) easily. It is not a mask for refinement. We modified the figure S3 legend to better describe this. As the reviewer suggested, we also showed the mask used in the last step of refinement in Figure S3. This mask excluded the intracellular portion of PAC TMD.

4. While not absolutely necessary, it could be helpful to mention for those unfamiliar with this protein family that it is also referred to as ASOR.

Thank you for pointing this out, we have mentioned that this protein family is also referred to as ASOR in the introduction.

5. Table S1, map resolution range: is 246 A a typo? This seems unusually low.

We thank the reviewers for pointing this out. This is indeed a typo and we have fixed this in Table S1.

Reviewer #3 (Recommendations for the authors):

1) The authors need to address the subcellular localization of PI(4,5)P2 and why their findings are surprising. Although they cite previous studies that have identified PI(4,5)P2 on the outer leaflet of the plasma membrane, it is a minor component of total PIP2 (see Yoneda et al. 2020, Figure 1). The localization and function of cellular PIP2 has been extensively studied (reviewed in Schink et al. 2016, PMID 27576122) and few roles for extracellular/lumenal PIP2 have been described to date. It is unlikely (albeit possible) that a native regulatory mechanism for PIP2 exists in this context, and the conclusions of the paper should reflect this fact.

Thank you for this insight, we agree that PIP2 predominantly localizes to the inner leaflets of the cell membrane. We have further clarified in the Discussion section of our paper that the physiological relevance (if any exists) of PIP2 inhibition of the PAC channel is unclear. Nevertheless, the novel lipid-binding pocket is a relevant discovery that can be exploited for targeted inhibition of the PAC channel.

2) The density of PAC with PIP2 (Figure S4) does not support the placement of the PIP2 headgroup. The authors acknowledge this fact with the following points in the Results section: "it is by no means unambiguous due to the limited local map resolution" and "the phosphatidyl group is reasonably well defined… in contrast, the inositol 4,5-bisphosphate moiety is not resolved". Confusingly, the authors also state that the deposited model does not contain the inositol headgroup (Figure 3A) but the attached validation files indicate that it has been (Molecule 3, PIO "Ligand of interest"). The authors need to decide whether their experimentally resolved data supports the positioning of bound PIP2 in the PAC structure (Figure 3A-C) or does not (the main text and figure legends, Figure S4). In doing so, the authors should consider the possibility of contaminating ligands from the other lipids (e.g. phosphatidic acid) in their preparation. Furthermore, in absence of supporting data, Figure 3C should be excluded from the manuscript. While it is apparent that the modeled basic residues are important for PAC inhibition by PIP2 (Figure 3E) and the authors are careful to note that the model is used to highlight the local biochemical (electrostatic) environment, the presentation of the figure (e.g. distance lines for electrostatic interactions) suggests more certainty than is warranted. Finally, note the pKA of inositol phosphates (Kooijman et al. 2009, PMID: 19725516); they will be partially protonated at pH 4.

We have revised Figure 3C to show the density of the lipid and important residues nearby. In our initial manuscript, we already acknowledged the fact that the assignment of PIP2 into the density is not unambiguous based on the cryo-EM map. However, the biochemical environment of the binding pocket, as well as the subsequent mutagenesis data support such a PIP2 binding site. We now re-wrote the paragraph to make this even clearer.

We thank the reviewer for pointing out the issue of PIO in the deposited model. We used the wrong model containing the head group, which is intended to be used only for making illustrations, for validation. We have now uploaded a new validation report using the correct model.

We acknowledge the referenced literature (Kooijman et al. 2009, PMID: 19725516) that the phosphate group may be partially protonated at pH 4, but this study is unable to reliably estimate the pKa2 of PI(4,5)P2 and the pKa1 is not studied. Moreover, in Figure 7 of the paper, no major difference is observed in the charge status of PI(4,5)P2 at pH 4-5, suggesting that the ionization status of PIP2 doesn’t change in the experimental condition investigated in our study. In a more recent review of PI(4,5)P2, it was suggested that at pH 4-5, both of the phosphomonoester groups are mono-protonated (Luís Borges-Araújo and Fabio Fernandes 2020, PMID: 32858905). Therefore, a net charge of -2 is present in the head group of PI(4,5)P2 under our experimental conditions, which allowed the molecule to interact favorably with the positively charged binding pocket (Figure 3C).

https://doi.org/10.7554/eLife.83935.sa2

Article and author information

Author details

  1. Ljubica Mihaljević

    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, United States
    Contribution
    Conceptualization, Data curation, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing – original draft, Writing – review and editing
    Contributed equally with
    Zheng Ruan
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3697-7767

  2. Zheng Ruan

    Department of Structural Biology, Van Andel Institute, Grand Rapids, United States
    Contribution
    Conceptualization, Data curation, Software, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing – review and editing
    Contributed equally with
    Ljubica Mihaljević
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-4412-4916

  3. James Osei-Owusu

    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, United States
    Contribution
    Data curation, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared

  4. Wei Lü

    Department of Structural Biology, Van Andel Institute, Grand Rapids, United States
    Contribution
    Conceptualization, Resources, Supervision, Funding acquisition, Project administration, Writing – review and editing
    For correspondence
    wei.lu@vai.org
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3009-1025

  5. Zhaozhu Qiu

    1. Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, United States
    2. Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, United States
    Contribution
    Conceptualization, Resources, Supervision, Funding acquisition, Project administration, Writing – review and editing
    For correspondence
    zhaozhu@jhmi.edu
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-9122-6077

Funding

Boehringer Ingelheim Fonds (Graduate Student Fellowship)

  • Ljubica Mihaljević

National Institute of General Medical Sciences (T32 GM007445 Graduate Training Program)

  • Ljubica Mihaljević

American Heart Association (Postdoctoral Fellowship grant 20POST35120556)

  • Zheng Ruan

National Institutes of Health (grant K99NS128258)

  • Zheng Ruan

American Heart Association (Predoctoral Fellowship grant 18PRE34060025)

  • James Osei-Owusu

National Institutes of Health (grant R01NS112363)

  • Wei Lü

McKnight Foundation (McKnight Scholar Award)

  • Zhaozhu Qiu

Alfred P. Sloan Foundation (Sloan Research Fellowship)

  • Zhaozhu Qiu

Esther A. and Joseph Klingenstein Fund (Klingenstein-Simons Fellowship)

  • Zhaozhu Qiu

National Institutes of Health (grant R35GM124824)

  • Zhaozhu Qiu

National Institutes of Health (grant R01NS118014)

  • Zhaozhu Qiu

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We thank the Qiu lab for thoughtful discussions. We thank G Zhao and X Meng for support with preliminary cryo-EM grid screening at the David Van Andel Advanced Cryo-Electron Microscopy Suite. L.M. is supported by a Boehringer Ingelheim Fonds (BIF) and National Institute of General Medical Sciences, T32 GM007445 (to the BCMB graduate training program). Z.R. is supported by an American Heart Association (AHA) postdoctoral fellowship (grant 20POST35120556) and the National Institute of Health (NIH) (grant K99NS128258). J O.-O. is supported by an AHA predoctoral fellowship (grant 18PRE34060025). W.L. is supported by the NIH (grant R01NS112363). Z.Q. is supported by a McKnight Scholar Award, a Klingenstein-Simon Scholar Award, a Sloan Research Fellowship in Neuroscience, and NIH grants (R35GM124824 and R01NS118014). A portion of this research was supported by NIH grant U24GM129547 and performed at the PNCC at OHSU and accessed through EMSL (grid.436923.9), a DOE Office of Science User Facility sponsored by the Office of Biological and Environmental Research.

Senior Editor

  1. Richard W Aldrich, The University of Texas at Austin, United States

Reviewing Editor

  1. Andrés Jara-Oseguera, The University of Texas at Austin, United States

Reviewers

  1. Andrés Jara-Oseguera, The University of Texas at Austin, United States
  2. Valeria Kalienkova, University of Groningen, Netherlands

Version history

  1. Received: October 4, 2022
  2. Preprint posted: October 7, 2022 (view preprint)
  3. Accepted: December 18, 2022
  4. Accepted Manuscript published: January 12, 2023 (version 1)
  5. Version of Record published: January 25, 2023 (version 2)

Copyright

© 2023, Mihaljević, Ruan et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. Ljubica Mihaljević
  2. Zheng Ruan
  3. James Osei-Owusu
  4. Wei Lü
  5. Zhaozhu Qiu
(2023)
Inhibition of the proton-activated chloride channel PAC by PIP2
eLife 12:e83935.
https://doi.org/10.7554/eLife.83935

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    Xiaoxuan Lin, Patrick R Haller ... Tobin R Sosnick
    Research Article

    Prestin responds to transmembrane voltage fluctuations by changing its cross-sectional area, a process underlying the electromotility of outer hair cells and cochlear amplification. Prestin belongs to the SLC26 family of anion transporters yet is the only member capable of displaying electromotility. Prestin’s voltage-dependent conformational changes are driven by the putative displacement of residue R399 and a set of sparse charged residues within the transmembrane domain, following the binding of a Cl− anion at a conserved binding site formed by the amino termini of the TM3 and TM10 helices. However, a major conundrum arises as to how an anion that binds in proximity to a positive charge (R399), can promote the voltage sensitivity of prestin. Using hydrogen–deuterium exchange mass spectrometry, we find that prestin displays an unstable anion-binding site, where folding of the amino termini of TM3 and TM10 is coupled to Cl− binding. This event shortens the TM3–TM10 electrostatic gap, thereby connecting the two helices, resulting in reduced cross-sectional area. These folding events upon anion binding are absent in SLC26A9, a non-electromotile transporter closely related to prestin. Dynamics of prestin embedded in a lipid bilayer closely match that in detergent micelle, except for a destabilized lipid-facing helix TM6 that is critical to prestin’s mechanical expansion. We observe helix fraying at prestin’s anion-binding site but cooperative unfolding of multiple lipid-facing helices, features that may promote prestin’s fast electromechanical rearrangements. These results highlight a novel role of the folding equilibrium of the anion-binding site, and help define prestin’s unique voltage-sensing mechanism and electromotility.

    1. Biochemistry and Chemical Biology
    2. Structural Biology and Molecular Biophysics

    The neuronal calcium sensor NCS-1 regulates the phosphorylation state and activity of the Ga chaperone and GEF Ric-8A

    Daniel Muñoz-Reyes, Levi J McClelland ... Maria Jose Sanchez-Barrena
    Research Article

    The Neuronal Calcium Sensor 1, an EF-hand Ca2+ binding protein, and Ric-8A coregulate synapse number and probability of neurotransmitter release. Recently, the structures of Ric-8A bound to Ga have revealed how Ric-8A phosphorylation promotes Ga recognition and activity as a chaperone and guanine nucleotide exchange factor. However, the molecular mechanism by which NCS-1 regulates Ric-8A activity and its interaction with Ga subunits is not well understood. Given the interest in the NCS-1/Ric-8A complex as a therapeutic target in nervous system disorders, it is necessary to shed light on this molecular mechanism of action at atomic level. We have reconstituted NCS-1/Ric-8A complexes to conduct a multimodal approach and determine the sequence of Ca2+ signals and phosphorylation events that promote the interaction of Ric-8A with Ga. Our data show that the binding of NCS-1 and Ga to Ric-8A are mutually exclusive. Importantly, NCS-1 induces a structural rearrangement in Ric-8A that traps the protein in a conformational state that is inaccessible to Casein Kinase II-mediated phosphorylation, demonstrating one aspect of its negative regulation of Ric-8A-mediated G-protein signaling. Functional experiments indicate a loss of Ric-8A GEF activity towards Ga when complexed with NCS-1, and restoration of nucleotide exchange activity upon increasing Ca2+ concentration. Finally, the high-resolution crystallographic data reported here define the NCS-1/Ric-8A interface and will allow the development of therapeutic synapse function regulators with improved activity and selectivity.