TRIM5 proteins are restriction factors that block retroviral infections by binding viral capsids and preventing reverse transcription. Capsid recognition is mediated by C-terminal domains on TRIM5α (SPRY) or TRIMCyp (cyclophilin A), which interact weakly with capsids. Efficient capsid recognition also requires the conserved N-terminal tripartite motifs (TRIM), which mediate oligomerization and create avidity effects. To characterize how TRIM5 proteins recognize viral capsids, we developed methods for isolating native recombinant TRIM5 proteins and purifying stable HIV-1 capsids. Biochemical and EM analyses revealed that TRIM5 proteins assembled into hexagonal nets, both alone and on capsid surfaces. These nets comprised open hexameric rings, with the SPRY domains centered on the edges and the B-box and RING domains at the vertices. Thus, the principles of hexagonal TRIM5 assembly and capsid pattern recognition are conserved across primates, allowing TRIM5 assemblies to maintain the conformational plasticity necessary to recognize divergent and pleomorphic retroviral capsids.https://doi.org/10.7554/eLife.16269.001
After infecting a cell, a virus reproduces by forcing the cell to produce new copies of the virus, which then spread to other cells. However, cells have evolved ways to fight back against these infections. For example, many mammalian cells contain proteins called restriction factors that prevent the virus from multiplying. The TRIM5 proteins form one common set of restriction factors that act against a class of viruses called retroviruses.
HIV-1 and related retroviruses have a protein shell known as a capsid that surrounds the genetic material of the virus. The capsid contains several hundred repeating units, each of which consists of a hexagonal ring of six CA proteins. Although this basic pattern is maintained across different retroviruses, the overall shape of the capsids can vary considerably. For instance, HIV-1 capsids are shaped like a cone, but other retroviruses can form cylinders or spheres.
Soon after the retrovirus enters a mammalian cell, TRIM5 proteins bind to the capsid. This causes the capsid to be destroyed, which prevents viral replication. Previous research has shown that several TRIM5 proteins must link up with each other via a region of their structure called the B-box 2 domain in order to efficiently recognize capsids. How this assembly process occurs, and why it enables the TRIM5 proteins to recognize different capsids was not fully understood. Now, Li, Chandrasekaran et al. (and independently Wagner et al.) have investigated these questions.
Using biochemical analyses and electron microscopy, Li, Chandrasekaran et al. found that TRIM5 proteins can bind directly to the surface of HIV-1 capsids. Several TRIM5 proteins link together to form large hexagonal nets, in which the B-box domains of the proteins are found at the points where three TRIM5 proteins meet. This arrangement mimics the pattern present in the HIV-1 capsid, and just a few TRIM5 rings can cover most of the capsid.
Li, Chandrasekaran et al. then analysed TRIM5 proteins from several primates, including rhesus macaques, African green monkeys and chimpanzees. In all cases analyzed, the TRIM5 proteins assembled into hexagonal nets, although the individual units within the net did not have strictly regular shapes. These results suggest that TRIM5 proteins assemble a scaffold that can deform to match the pattern of the proteins in the capsid. Further work is now needed to understand how capsid recognition is linked to the processes that disable the virus.https://doi.org/10.7554/eLife.16269.002
Mammalian hosts have evolved a series of different innate immune strategies to combat retroviruses (reviewed in [Altfeld and Gale, 2015; Bieniasz, 2003, 2004; Fitzgerald et al., 2014; Harris et al., 2012; Neil and Bieniasz, 2009; Rustagi and Gale, 2014; Sparrer and Gack, 2015; van Montfoort et al., 2014; Yoo et al., 2014]). TRIM5α and the related TRIMCyp protein (collectively TRIM5) are restriction factors that recognize the capsid surfaces of incoming retroviral core particles, induce their dissociation, and inhibit reverse transcription (Sayah et al., 2004; Stremlau et al., 2004; 2006). The mechanistic basis for core inactivation is not yet well established, but current models invoke the involvement of proteasomes (Anderson et al., 2006; Campbell et al., 2008; Diaz-Griffero et al., 2007; Kutluay et al., 2013; Lukic et al., 2011; Rold and Aiken, 2008; Wu et al., 2006), autophagosomes (Mandell et al., 2014a; 2014b), and/or the establishment of a general antiviral state (Pertel et al., 2011).
Like other members of the tripartite motif (TRIM) family (Reymond et al., 2001), TRIM5 proteins comprise a RING E3 ubiquitin (Ub) ligase domain (Meroni and Diez-Roux, 2005; Yamauchi et al., 2008), an L1 linker, a B-box 2 self-assembly domain (Diaz-Griffero et al., 2009; Javanbakht et al., 2005; Li and Sodroski, 2008), an antiparallel dimeric coiled-coil, and an L2 linker that folds back on the coiled-coil (Goldstone et al., 2014; Li et al., 2014; Sanchez et al., 2014; Weinert et al., 2015) (Figure 1A). TRIM5 proteins also contain one of two different C-terminal viral core recognition domains, a B30.2/SPRY domain in TRIM5α (hereafter termed SPRY) or a cyclophilin A (CypA) domain in TRIMCyp (Brennan et al., 2008; Newman et al., 2008; Nisole et al., 2004; Sayah et al., 2004; Stremlau et al., 2005; 2006; Virgen et al., 2008).
TRIM5 proteins act by binding the outer capsid shell of the viral core (Biris et al., 2013; Black and Aiken, 2010; Diaz-Griffero et al., 2006b; Kar et al., 2008; Kovalskyy and Ivanov, 2014; Langelier et al., 2008; Sayah et al., 2004; Sebastian and Luban, 2005; Stremlau et al., 2006; Zhao et al., 2011). The capsid protects and organizes the internal ribonucleocapsid, which comprises the viral NC protein, the RNA genome, and associated replicative enzymes. Closed retroviral capsids are constructed from several hundred CA protein hexamers and exactly 12 CA pentamers ([Ganser et al., 1999; Gres et al., 2015; Li et al., 2000; Obal et al., 2015; Pornillos et al., 2011; Zhao et al., 2013] and reviewed in [Ganser-Pornillos et al., 2012; Zhang et al., 2015]). Although all retroviral capsids are organized following these principles, individual capsids are unique, asymmetric objects that can differ in hexamer numbers and pentamer distributions (Benjamin et al., 2005; Briggs et al., 2006; Butan et al., 2008; Ganser-Pornillos et al., 2004; Heymann et al., 2008). For example, HIV-1 capsids are typically conical, but their sizes and cone angles can vary, and cylindrical and spherical capsids also form (Benjamin et al., 2005; Briggs et al., 2006; Briggs et al., 2003; Ganser-Pornillos et al., 2004; Heymann et al., 2008; Welker et al., 2000). Indeed, spherical and cylindrical capsids predominate in other retroviral genera, and capsid surface properties can vary considerably because CA proteins from different genera share low sequence identity (Berthet-Colominas et al., 1999; Campos-Olivas et al., 2000; Cornilescu et al., 2001; Ganser et al., 1999; Jin et al., 1999; Khorasanizadeh et al., 1999; Kingston et al., 2000; Momany et al., 1996; Mortuza et al., 2008; Mortuza et al., 2004; von Schwedler et al., 1998; Zlotnick et al., 1998).
To function effectively, individual TRIM5 proteins must overcome these variations in retroviral capsid shape and sequence (Hatziioannou et al., 2003; Wilson et al., 2008). We, and others, have proposed that TRIM5 proteins recognize pleomorphic capsids by recognizing repeating patterns on the capsid surface (Biris et al., 2012; Ganser-Pornillos et al., 2011; Goldstone et al., 2014; Yang et al., 2012). This model supposes that flexible loops on the SPRY and CypA domains can adopt multiple different conformations and can bind weakly to conserved elements on the capsid surfaces (Biris et al., 2012; Caines et al., 2012; Kovalskyy and Ivanov, 2014; Price et al., 2009; Song et al., 2005a; Stremlau et al., 2005; Ylinen et al., 2010). These weak interactions are then amplified by TRIM5 assembly into a higher-order hexagonal lattice, which positions arrays of SPRY/CypA domains to interact with repeating epitopes on the capsid surfaces (Ganser-Pornillos et al., 2011; Li and Sodroski, 2008).
This 'pattern recognition' model has been supported by biochemical and structural analyses of a TRIM5 protein construct called TRIM5-21R, which is an artificial chimera in which the RING domain from human TRIM21 replaces the RING domain of rhesus TRIM5α (Diaz-Griffero et al., 2006a; Kar et al., 2008; Langelier et al., 2008). The TRIM5-21R construct retains HIV-1 restriction activity, and has been used in several studies owing to its unusually favorable stability, solubility and assembly properties. Consistent with the pattern recognition model, TRIM5-21R was shown to assemble into open hexagonal lattices, both alone and on the surface of 2D CA crystals that mimic the surface of the HIV-1 capsid (Ganser-Pornillos et al., 2011). TRIM5-21R assemblies could be microns in size but lacked strict long-range order, and 2D projections could therefore only be reconstructed to a resolution of ~7.5 nm. Domain positions therefore had to be inferred, and were interpreted in the absence of high-resolution information on the structure of the TRIM5 protein core.
Technical challenges in purifying authentic HIV-1 cores have also been a significant experimental limitation, and all published biochemical and structural studies of TRIM5α-capsid interactions have therefore either employed crude viral core preparations or artificial mimics of the capsid surface (Black and Aiken, 2010; Ganser-Pornillos et al., 2011; Langelier et al., 2008; Sebastian and Luban, 2005; Stremlau et al., 2006; Zhao et al., 2011). Thus, the interactions between authentic viral capsids and TRIM5 proteins have yet to be investigated biochemically or structurally. To address these different shortcomings, we have developed methods for preparing authentic recombinant TRIM5 proteins, co-assemblies of TRIM5 and CA proteins, and stable HIV-1 cores. These reagents were then used to demonstrate that TRIM5 proteins form hexagonal arrays on HIV-1 capsids.
A composite model for the domain organization within the TRIM5α dimer is shown in Figure 1A. We (Sanchez et al., 2014), and others (Goldstone et al., 2014; Weinert et al., 2015), have suggested that these dimers form the edges of the hexameric rings observed within the hexagonal TRIM5-21R lattice (modeled in Figure 1B). This model is attractive because the edges of each hexagon are ~19 nm long, which would accommodate the antiparallel TRIM5α coiled-coil (~17 nm), and the RING and B-box 2 domains would associate at the three-fold vertices, which is consistent with the trimeric B-box 2 domain structure presented in the accompanying paper (Wagner et al., 2016). Finally, the L2 linkers fold back and form a four-helix bundle at the center of the coiled-coil, and this platform could, in principle, buttress and orient the TRIM5α SPRY domains. None of the domain positions have been determined experimentally, however, and we therefore began our studies by defining the location of the SPRY domains within the hexagonal TRIM5-21R lattice.
To visualize TRIM5-21R assemblies in three dimensions and define the SPRY domain positions, we generated electron cryotomograms (ECT) from tilt series of vitrified 2D crystals of both full length TRIM5-21R (Figure 1C) and a construct that lacked the SPRY domain (TRIM5-21RΔSPRY, residues 1–300, Figure 1D). The 3D reconstructions were refined and improved by subtomogram averaging of densities centered at equivalent lattice vertices. As expected, TRIM5-21R and TRIM5-21RΔSPRY both assembled into similar planar lattices of hexagonal rings, with inter-ring spacings and protein densities matching those of the previous 2D projection structures (Ganser-Pornillos et al., 2011). Difference density maps clearly revealed that the SPRY domains are located at the center of each hexagon edge (Figure 1E), thereby supporting the model shown in Figure 1B.
Although the paracrystalline arrays of TRIM5-21R exhibited long-range order, they diffracted poorly, suggesting variability within the lattice. To quantify this variability, we performed a nearest neighbor analysis of the refined positions of the lattice vertices used for subtomogram averaging. The relative positions of 153 vertices in the TRIM5-21R 2D crystals were used to define individual hexamer edge lengths and angles (see Figure 1F). The length distribution of hexamer edges was centered about a mean of 19 nm, but individual lengths varied by up to ±5 nm (Figure 1G, upper panel). Similarly, the distribution of hexamer vertex angles was centered about 120°, but varied by up to ±20° (Figure 1G, lower panel). Thus, individual rings within the TRIM5 lattice exhibited considerable conformational variability, explaining the poor crystalline order and modest diffraction resolution.
Recombinant owl monkey TRIMCyp has been purified (Pertel et al., 2011), but TRIM5α proteins are more challenging to purify because these proteins tend to self-assemble, both in cells and in vitro. Hence, previous biochemical and structural studies of TRIM5α proteins have been performed with impure proteins, protein fragments, or non-native chimeric constructs (Biris et al., 2012; Goldstone et al., 2014; Kar et al., 2008; Langelier et al., 2008; Sanchez et al., 2014; Yang et al., 2012; Ganser-Pornillos et al., 2011). To overcome this limitation, we tested a variety of different expression and purification conditions, with the goal of developing a general method for preparing milligram quantities of authentic, full-length primate TRIM5α and TRIMCyp proteins.
The strategy that was ultimately successful entailed expressing TRIM5 proteins in insect cells using a baculoviral expression system. As described in greater detail in the Materials and methods, expressed TRIM5 proteins formed cytoplasmic bodies that could be solubilized by lysing the cells in a low ionic strength, alkali buffer that contained the non-ionic detergent Triton X-100, as well as a non-detergent small molecule, sulfobetaine-256 (NDSB-256) that has previously been shown to inhibit protein aggregation (Sainsbury et al., 2008; Vuillard et al., 1995). Once solubilized, primate TRIM5 proteins typically remained dimeric and soluble under low salt, alkaline conditions in the absence of Triton X-100 and NDSB-256, even at concentrations greater than 1 mg/ml. The proteins could therefore be purified, provided they were maintained at high pH, low salt and/or low protein concentrations.
Our stepwise protein purification protocol is illustrated for rhesus TRIM5α in Figure 2A. Briefly, various N-terminal OneSTrEP-FLAG- (OSF-) or C-terminal FLAG-OneSTrEP- (FOS-) tagged TRIM5 proteins were initially purified using Strep-Tactin affinity chromatography, the affinity tag was removed by HRV14-3C protease treatment, and the proteins were then purified to homogeneity by anion exchange and gel filtration chromatography. Analogous approaches were used to express and purify wild type and mutant TRIM5α proteins from rhesus macaques (Macaca mulatta, here abbreviated TRIM5αrh), African green monkeys (Chlorocebus pygerythrus, TRIM5αAGMpyg), chimpanzees (Pan troglodytes, TRIM5αcpz), humans (Homo sapiens, TRIM5αhu), and the TRIMCyp protein from owl monkeys (Aotus trivirgatus, TRIMCyp). Yields ranged between 1.3 and 9.6 mg/L of insect cell cultures, and all of the proteins eluted with similar retention times during the final gel filtration chromatography step, indicating that they were all dimers of similar shape. All of the proteins could be purified to >95% purity (Figure 2B) with the exception of TRIMCyp, where our preparations also contained breakdown contaminants that mapped to proteolytic cleavage at residues Lys283 and Gln287 (not shown). These breakdown contaminants were eliminated by creating a mutant construct that expressed TRIMCypK283D,Q287D (Figure 2B, lane 4). These mutations are not expected to affect functionally relevant properties of the protein because TRIMCypK283D,Q287D retains potent HIV-1 restriction activity (Figure 2—figure supplement 1).
To determine whether the ability to assemble into hexagonal nets is a conserved property of authentic TRIM5 proteins, we screened for conditions that promoted assembly of different primate TRIM5 proteins, using negative stain EM imaging to assay assembly states. These screens identified conditions under which two of the TRIM5 proteins, TRIM5αAGMpyg (Figure 2C) and TRIMCyp (Figure 2D) spontaneously formed 2D hexagonal assemblies that were similar in appearance to those formed by TRIM5-21R (Ganser-Pornillos et al., 2011). Assembly efficiencies varied, however, as TRIM5αAGMpyg assembled very efficiently under the same conditions as TRIM5-21R, whereas TRIMCyp assembled inefficiently and required additional precipitants (see Materials and methods). Negatively stained 2D crystals of TRIM5αAGMpyg and TRIMCyp were imaged and processed to generate Fourier-filtered 2D projection reconstructions (Figure 2C,D; bottom). Both TRIM5 proteins formed lattices comprising open hexameric rings that were similar in appearance and size to the TRIM5-21R rings, demonstrating that diverse TRIM5 proteins from different primates that share 73% pairwise identity across their TRIM domains share the ability to assemble into analogous hexagonal nets.
The pattern recognition model for TRIM5 restriction predicts that binding to the surface of the viral capsid promotes hexagonal TRIM5 assembly. We therefore tested whether hexagonal 2D crystals of HIV-1 CA, which mimic the capsid surface, could promote the assembly of three different restricting TRIM5 proteins; TRIM5αrh, TRIMCypK283D,Q287D, and TRIM5αhu,R332P, and two different non-restricting TRIM5 proteins; wild type TRIM5αhu and TRIM5αcpz (Hatziioannou et al., 2004; Nisole et al., 2004; Sayah et al., 2004; Song et al., 2005b; Stremlau et al., 2004; 2005; Yap et al., 2005). To test for templated assembly of TRIM5 proteins, soluble dimeric proteins were incubated together with preassembled 2D CA crystals under solution conditions that were sufficiently stringent to prevent untemplated assembly. TRIM5αAGMpyg was not used in these studies because it assembled very robustly even in the absence of a template.
As shown in Figure 3, the three restricting TRIM5 proteins assembled into visible hexagonal nets on the surfaces of preformed HIV-1 CA crystals, whereas templated assembly was not observed for either one of the non-restricting TRIM5 proteins (Figure 3C and data not shown). Templated assembly therefore correlated well with restriction activity, emphasizing the coupling of CA binding and TRIM5 lattice assembly. Computed Fourier transforms of the images of decorated crystals (Figure 3, insets) revealed well-defined first- and second-order reflections from the smaller underlying CA lattice (red and blue), as well as more diffuse peaks (TRIM5αrh and TRIMCypK283D,Q287D, green) or a powder diffraction ring (TRIM5αhu,R332P) corresponding to the first-order reflections from the hexagonal TRIM5 lattices. Thus, all three restricting TRIM5 proteins bound the CA surfaces and assembled into hexagonal nets that were clearly visible, but lacked extensive crystalline order.
The helical tubes formed by pure recombinant HIV-1 CA provide another regularized model for the curved, symmetric arrays of CA hexagons on conical viral capsid surfaces (Campbell and Vogt, 1995; Li et al., 2000). We employed a sucrose co-sedimentation assay to test whether the restricting TRIM5αAGMpyg and TRIMCypK283D,Q287D proteins bound disulfide-crosslinked helical tubes formed by a mutant HIV-1 CA protein that assembled into discrete helical tubes stabilized by intrahexamer disulfide crosslinks (CAA14C,E45C,A92E) (Byeon et al., 2009; Ganser-Pornillos et al., 2011; Langelier et al., 2008; Li et al., 2000; Pornillos et al., 2009; 2010; Zhao et al., 2011). Both TRIM5αAGMpyg and TRIMCypK283D,Q287D bound the CA tubes, as judged by their co-sedimentation through the sucrose cushion when the CA tubes were present, but not when they were absent (compare the 'pellet' fractions in lanes 1 vs. 2 and lanes 5 vs. 6 in Figure 4—figure supplement 1A). Binding was specific because TRIM5αAGMpyg did not co-sediment with CA tubes when the SPRY domain was removed (compare lanes 2 vs. 4) and because TRIMCypK283D,Q287D did not co-sediment with CA tubes in the presence of cyclosporine A, which competitively inhibits the CypA-CA interaction (compare lanes 6 vs. 7). Thus, pure recombinant TRIM5 proteins bind the hexagonal lattices of both helical CA tubes and 2D CA crystals.
Negative stain and deep-etch electron microscopy were used to image the TRIM5-decorated HIV-1 CA tubes. Four restricting TRIM5 proteins, TRIM5αAGMpyg, TRIMCypK283D,Q287D, TRIM5αrh, and TRIM5αhu,R332P, formed thin ring-like decorations on the surfaces of CA tubes (Figure 4—figure supplement 1B). The TRIM5 decorations typically appeared as light, string-like nets against the darker underlying CA tubes when the assemblies were stained with either uranyl acetate (UA) or phosphotungstate (PTA). Equivalent decorations were not observed for control CA tubes alone or for CA tubes plus TRIM5αhu, which does not restrict HIV-1. TRIM5 decoration of CA tubes therefore correlated with restriction activity.
Deep-etch EM images often exhibit even greater contrast than negative stain transmission EM images, and this effect was evident in deep-etch images of undecorated HIV-1 CA tubes, where rows of individual CA hexamers were readily visible (Figure 4A, upper panel). Strings and rings of TRIM5αAGMpyg were often readily visible on the decorated CA tube surfaces, and networks of rings were sometimes observable (Figure 4A, lower panel). Hence, TRIM5 proteins can form hexagonal nets on the surfaces of helical HIV-1 CA tubes.
The efficiency of TRIM5 assembly on disulfide-crosslinked CA tubes was relatively low, which may explain why the decorations were not noted in previous studies. We therefore screened additional assembly conditions to determine the source of this variability. These experiments revealed that co-incubation of native CA protein with TRIM5α under low ionic strength conditions produced CA tubes that were extensively decorated with TRIM5α. Co-assembly was reproducible, and both tagged and untagged TRIM5-21R, TRIM5AGMpyg, and TRIM5rh proteins formed ring-like decorations on CA tube surfaces at a variety of different CA/TRIM5 molar ratios (Figure 4B, data not shown, and Wagner et al., 2016). The TRIM5αAGMpyg inter-ring spacing distribution on the tubes centered at 30–35 nm, as was also the case for TRIM5αAGMpyg assemblies on pre-formed disulfide-crosslinked CA tubes (Figure 4C). In all cases, the rings were irregular and their spacings varied between 15 and 55 nm. Electron cryotomography (ECT) analyses similarly revealed extensive networks of hexagonal nets coating individual cylinders (Figure 4D and Video 1). As seen for TRIM5-21R 2D crystals, the hexamer edge lengths measured from three-fold vertices selected from the tomogram were predominantly ~19 nm, but varied between 15 to 23 nm. Similarly, the hexamer vertex angles averaged ~120°, but ranged from 80° to 160° (Figure 4E). The flexibility of the TRIM5 assembly may reflect flexing of the coiled-coil domains and/or the hinge between B-box 2 and coiled-coil domains (Wagner et al., 2016). In summary, TRIM5 proteins consistently formed hexagonal arrays on curved HIV-1 CA lattices, and the TRIM5 lattice was more extensive when the two proteins co-assembled together, presumably because the two lattices could template one another and thereby optimize their interactions.
A central goal of our studies was to analyze TRIM5 binding to authentic viral capsids, both biochemically and by direct imaging. This goal is technically challenging owing to the inherent instability of viral core particles. We reasoned that this challenge might be overcome by disulfide-crosslinking the capsid shell to increase its stability. This strategy was particularly attractive because previous studies showed that Cys residues substituted at CA positions Ala14 and Glu45 crosslinked efficiently when CA hexamers were assembled in vitro (Pornillos et al., 2009; 2010). We therefore tested the effect of introducing these substitutions into authentic HIV-1 capsids.
Normal levels of viral particles were produced from 293T cells that expressed an HIV-1NL4-3∆R8.2 proviral expression vector that encoded the mutant CAA14C,E45C protein (not shown). Wild type and mutant viral cores were isolated by centrifugation of virions through a detergent layer to remove the outer viral membrane and then directly into a 30–70% sucrose gradient, where viral cores concentrated at a density of 1.22–1.27 g/ml (fractions 10–12, highlighted in pink in Figure 5A). As reported previously (Forshey et al., 2002; Kotov et al., 1999), wild type cores could also be isolated using this procedure (see Figure 5B). However, recovered core yields were consistently modest in our hands (0.2 ± 0.1% based upon total virion CA), apparently because most of the CA molecules dissociated from the core and migrated to the top of the gradient during purification (Figure 5A, left panel). In contrast, nearly all of the CAA14C,E45C protein migrated toward the bottom of the gradient when cores were isolated from mutant virions (Figure 5A, right panel). Much of this CA protein was present within small incomplete, broken, or spherical assemblies that concentrated at densities of 1.18–1.21 g/ml (gradient fractions 6–9, Figure 5A, right panel and see Figure 5—figure supplement 1). These non-native assemblies probably arose from spurious crosslinking of CA hexamers in the free intraviral pool of CA molecules that are excluded from the mature HIV-1 capsid (Benjamin et al., 2005; Briggs et al., 2004; Lanman et al., 2004; Monroe et al., 2010). Nevertheless, a substantial fraction of the CA protein also concentrated at the density expected for native core particles (fractions 10–12, highlighted in pink in Figure 5A, right panel). These 'hyperstable' cores were reproducibly recovered in higher yields (0.8 ± 1%) than wild type cores (0.2 ± 0.1%), and their morphologies were similar to wild type cores (Figure 5B, right panel). Consistent with the design, nearly all of the CA molecules within these fractions were crosslinked within stable hexamers, as analyzed by non-reducing SDS-PAGE and western blotting (Figure 5C). These experiments indicate that disulfide crosslinking occurs spontaneously in otherwise native and untreated HIV-1 capsids, and that the crosslinks stabilize the capsids without introducing any major morphological defects.
Hyperstable HIV-1 cores purified on sucrose gradients were not optimal for imaging studies because they aggregated and co-sedimented with vesicles and other impurities. To produce purer cores, we designed an alternative core affinity purification method that exploited the interaction between cyclophilin A (CypA) and HIV-1 CA (outlined in Figure 5—figure supplement 1D) (Franke et al., 1994; Gamble et al., 1996; Luban et al., 1993; Thali et al., 1994). Viral membranes were stripped by a brief Triton X-100 treatment and the liberated cores were then captured on magnetic Strep-Tactin beads derivatized with OSF-CypA. The immobilized cores were washed rigorously and then eluted with the small molecule cyclosporine A (CsA), which competitively inhibits the CypA-CA interaction and binds CypA ~700-fold more tightly than does CA (Figure 5D and Figure 5—figure supplement 1E) (Braaten et al., 1996; Franke and Luban, 1996; Gamble et al., 1996; Wear et al., 2005; Yoo et al., 1997). This method increased core yields by an additional four fold (3 ± 2% core recovery) and increased their purity (compare Figure 5D to Figure 5B, right panel). The method also reduced the fraction of broken cores, possibly because they were less stable and therefore removed during the extensive wash steps and/or because they bound less avidly to the matrix. To reduce core clustering, we introduced the CA A92E substitution within the exposed loop of HIV-1 CA. This mutation does not affect TRIM5α restriction (Li et al., 2006), and was previously shown to reduce the clustering of helical CA tubes, presumably by reducing overall surface hydrophobicity (Ganser-Pornillos et al., 2004; Li et al., 2000; Zhao et al., 2011). As shown in Figure 5E, the substitution also reduced the clustering of viral cores (compare Figures 5D and E), and did so without altering core morphology or reducing core yields (3 ± 1% core recovery).
In summary, dispersed hyperstable CAA14C,E45C,A92E cores could be purified by affinity chromatography in high yields. The purified cores contained the expected viral proteins as analyzed by SDS-PAGE with silver staining (Figure 5—figure supplement 1F), were hyperstable and fully disulfide crosslinked (Figure 5C), exhibited normal capsid morphologies (compare Figure 5E to Figure 5B), and spread diffusely on EM grids (Figure 5E).
The susceptibility of different retroviruses to restriction by different TRIM5 variants can vary dramatically and appears to be determined largely at the level of capsid recognition (Li et al., 2006; Ohkura et al., 2006; Perez-Caballero et al., 2005; Sebastian and Luban, 2005; Song et al., 2005a; Stremlau et al., 2004; 2005; 2006). Consistent with previous reports (Sayah et al., 2004; Song et al., 2005b; Stremlau et al., 2004), we found that TRIM5 proteins restricted the transduction of HeLa cells with an HIV-1 reporter vector, and the strength of restriction followed the order: TRIMCyp and TRIMCypK283D,Q287D>TRIM5αrh>TRIM5αAGMpyg, with no restriction observed for TRIM5αcpz or TRIM5αhu (Figure 2—figure supplement 1). A sucrose cushion co-sedimentation assay was again used to test whether pure recombinant TRIM5α proteins bound directly to hyperstable HIV-1 cores, and whether core binding correlated with restriction activity. These experiments were performed with two proteins that restrict HIV-1, TRIM5αAGMpyg and TRIM5αrh, and one that does not, TRIM5αcpz.
As shown in Figure 6A, the two restricting TRIM5αAGMpyg and TRIM5αrh proteins both co-pelleted with hyperstable HIV-1 cores and did not pellet in the absence of cores (compare lanes 1 vs. 2 and lanes 3 vs. 4). In contrast, the non-restricting TRIM5αcpz protein did not bind cores under the same conditions (compare lanes 5 vs. 6). These core binding experiments were performed in the presence of excess TRIM5α proteins, and the approximate stoichiometry of the pelleted core-TRIM5αAGMpyg complexes was estimated by comparing the levels of CA and TRIM5αAGMpyg to standard curves of known protein concentrations. The measured TRIM5αAGMpyg:CA ratio in these experiments was 1:7 ± 2 (n = 4). Based upon their relative sizes, we estimate that each TRIM5 ring will cover ~14 CA hexamers (Ganser-Pornillos et al., 2011). On the basis of an idealized binding model and the known stoichiometries of each ring (CA = 6, TRIM5α = 12), we estimate that a fully saturated capsid would have a TRIM5:CA ratio of ~1:14. Hence, two different restricting TRIM5α proteins can bind directly to hyperstable HIV-1 cores at near saturating levels in vitro, whereas the non-restricting TRIM5αcpz protein does not bind cores. Consistent with the solution binding experiments, negative stain electron microscopic images again revealed thin ring-like assemblies of TRIM5αrh proteins on the capsid surfaces of hyperstable viral cores (Figure 6B, compare the cores in the second and third rows with the undecorated cores in the first row).
Free and TRIM5αAGMpyg-decorated cores were also visualized in three dimensions by ECT (Figure 7 and Figure 7—figure supplement 1). Free hyperstable cores could be spherical, cylindrical, or conical, and general size distributions and lattice features were similar to native HIV-1 cores (Figure 7—figure supplement 1). Holes in the tips of some conical cores were also observed, supporting previous results suggesting that cores are frequently unclosed (Yu et al., 2013).
Samples in which cores were incubated with TRIM5αAGMpyg typically exhibited networks of densities at the air/water interface. These networks exhibited three-fold vertices in the plane of the interface that were similar to 2D hexagonal TRIM5α lattices but did not exhibit diffraction or crystalline order (Video 2). Approximately 12% of cores imaged were also decorated on their outer capsid surfaces with TRIM5αAGMpyg densities. Multiple extended density 'arms' approximately 19 nm in length were seen arranged in a roughly hexagonal pattern (Figure 7A, and Video 2).
The prevalence of TRIM5αAGMpyg at the air/water interface and relative paucity of TRIM5α-decorated cores suggested that previously core-bound TRIM5α was being lost to the air/water interface during plunge-freezing (Video 3). To reduce this problem, we crosslinked the core-TRIM5α complexes with ethylene glycol bis(sulfosuccinimidylsuccinate) (Sulfo-EGS) prior to plunge freezing. Even after crosslinking, a substantial amount of TRIM5α was still seen at the air/water interface, but now the majority of cores were decorated with TRIM5αAGMpyg. Analysis of the volume surrounding these cores revealed broken, but extensive TRIM5α hexagonal nets, which in some cases enveloped the entire capsid (Figure 7B, Figure 7—figure supplement 2, and Videos 4). TRIM5α nets on bona fide cores were irregular, but exhibited a similar distribution of hexamer edge lengths (20 ± 2 nm, n = 51) and vertex angles (120 ± 2°, n = 68) as CA/TRIM5 'co-assemblies' (Figure 7—figure supplement 3). In some cases, TRIM5α densities with a length of ~38 nm were observed on the capsid surface (data not shown). These longer densities might occur through the association of two sets of TRIM5α dimers via dimeric rather than trimeric B-box 2 domain interactions (Wagner et al., 2016). Despite these irregularities, we were able to perform coarse, rigid body fitting of the crystal structures of B-box 2 trimers and coiled-coil dimers into 3D density maps. As shown in Figure 7C, each edge was occupied with a TRIM5α coiled-coil dimer and the three-fold densities were occupied by three B-box 2 domains. The fitting revealed that TRIM5 hexagonal lattices are in good agreement with the crystal structures in dimensions and angles. Overall, our results indicate that TRIM5 proteins form flexible hexagonal nets on the capsid surface with their domain positions schematically shown in Figure 7D.
Our studies further support the prevailing models that TRIM5 restriction factors bind directly to the surfaces of incoming retroviral capsids and that restriction susceptibility is dictated at the level of capsid recognition (Li et al., 2006; Ohkura et al., 2006; Perez-Caballero et al., 2005; Sebastian and Luban, 2005; Song et al., 2005a; Stremlau et al., 2004; 2005; 2006). In addition, we find that the ability to assemble into hexagonal nets comprising open, six-sided rings is a conserved feature of multiple different primate TRIM5 proteins. Our EM analyses, together with recent crystal structures of fragments of non-assembling TRIM5 proteins that span the core coiled-coil and L2 linker regions (Goldstone et al., 2014; Sanchez et al., 2014), indicate that each ring edge is formed by a TRIM5 dimer that displays two SPRY (or CypA) recognition domains at its center. Most importantly, we find that capsid binding and TRIM5 assembly are coupled processes that cooperate to promote the recognition of pleomorphic retroviral cores with high affinity and specificity.
Through the course of our studies we developed and characterized two new sets of reagents for studying retroviral replication and restriction: hyperstable, disulfide-crosslinked HIV-1 capsids and pure recombinant primate TRIM5 proteins. The generation of hyperstable capsids was enabled by previous studies showing that Cys residues at CA positions 14 and 45 form disulfide bonds efficiently in vitro when these residues are closely juxtaposed within the CA hexamer (Pornillos et al., 2009; 2010). Our experiments demonstrate that these disulfides also form efficiently in the context of the intact HIV-1 capsid. A similar disulfide crosslinking strategy was also used to link CA trimers at cysteine positions 207 and 216 across the local three-fold axes of the HIV-1 capsid (Byeon et al., 2009; Zhao et al., 2011). We have compared these two different systems, as well as an alternative strategy in which CA hexamers were crosslinked by disulfide bonds between Cys residues at CA positions 42 and 54 (Pornillos et al., 2010). Disulfide bonds form readily within viral capsids in all three cases (Byeon et al., 2009; Pornillos et al., 2009; 2010; Zhao et al., 2011) (and data not shown), and we anticipate that the different crosslinking strategies could have distinct advantages depending upon the application. For example, we have confirmed the report that HIV-1 cores with trimerized CA proteins retain modest infectivity (Byeon et al., 2009), whereas infectivity is almost completely abolished when cores are crosslinked at either site in the CA hexamer. We also find, however, that viral core yields and stabilities are greater for the two hexamer crosslinking systems, and are highest for the Cys14/Cys45 system described here. Thus, these hyperstable capsids should be optimal for analyzing the binding of a series of proteins and drugs that have recently been described, including the proteins CPSF6 (Bhattacharya et al., 2014; Lee et al., 2010; Price et al., 2014), Nup153 (Bhattacharya et al., 2014; Di Nunzio et al., 2013; Matreyek et al., 2013; Price et al., 2014), and Nup358 (Bichel et al., 2013; Meehan et al., 2014; Schaller et al., 2011), and the inhibitors PF-74 (Bhattacharya et al., 2014; Blair et al., 2010; Fricke et al., 2013; Price et al., 2014) and BI-1 and BI-2 (Fricke et al., 2014; Lamorte et al., 2013; Price et al., 2014). Hyperstable capsids may also represent a useful starting point for the development of in vitro viral replication assays, particularly if the capsid disulfides can be reduced without inactivating the internal reverse transcriptase and integrase enzymes.
The development of systems for producing milligram quantities of pure recombinant primate TRIM5 proteins should similarly facilitate studies of restriction by advancing methods for protein detection and enabling new mechanistic and structural analyses. For example, our recombinant TRIM5αrh proteins have already been used successfully as antigens to generate monoclonal antibodies that can detect endogenous TRIM5α proteins (NIH AIDS Reagent Program and (Imam et al., 2016). Moreover, although structural studies of TRIM5 protein domains and fragments have made valuable contributions to our understanding of TRIM5 structure and enzymology, there are a number of indications that the different domains work together as an integrated machine (Ganser-Pornillos et al., 2011; Goldstone et al., 2014; Li et al., 2013; Li and Sodroski, 2008; Reymond et al., 2001; Sanchez et al., 2014). It will therefore also be important to study intact TRIM5 proteins, particularly to determine how capsid recognition is coupled to ubiquitin signaling (Fletcher et al., 2015; Pertel et al., 2011; Yudina et al., 2015).
Antiviral innate immune factors that function by recognizing retroviral capsids must overcome considerable sequence and structural variability. Primate TRIM5 proteins accomplish this task by coupling weak recognition of conserved capsid epitopes with hexagonal net assembly, thereby amplifying intrinsically weak binding affinities through avidity effects (Ganser-Pornillos et al., 2011; Price et al., 2009). Our studies confirm that hexagonal net assembly is a conserved property, but also reveal that the TRIM5 hexagonal nets are not highly regular. The lack of strict regularity in the TRIM5 net may be required to adapt to the lack of regularity in the opposing retroviral capsids, where every CA hexagon occupies a slightly different local environment and where pentagons and other kinds of lattice 'defects' are also prevalent (Byeon et al., 2009; Ganser-Pornillos et al., 2011; Gres et al., 2015; Hatziioannou et al., 2004; Obal et al., 2015; Pornillos et al., 2011; Yu et al., 2013; Zhao et al., 2013).
Consistent with a lattice assembly model, imaging studies have provided direct evidence that multiple TRIM5 molecules can bind continuously to incoming capsids (Campbell et al., 2008; Danielson et al., 2012; Lukic et al., 2011). The stoichiometry of TRIM5-capsid interactions within cells is not yet known, but we find that TRIM5 molecules can cover most of the capsid surface in vitro. A patch of just 4–6 TRIM5 rings covers about half of the capsid surface (see Figure 7), however, and would present ~40 recognition domains for avid capsid binding. Thus, the entire capsid probably does not need to be completely enveloped within a surrounding TRIM5 lattice for restriction to occur. Indeed, CA mixing studies have shown that efficient TRIM5 restriction can occur even when only 25% of the capsid subunits are competent for TRIM5 binding (Shi et al., 2013).
TRIM5-mediated restriction appears to proceed via a multi-step pathway in which capsid recognition is followed by steps that lead to capsid dissociation and inhibition of reverse transcription (Pertel et al., 2011; Stremlau et al., 2006). In cells, the later processes can be decoupled from the initial binding event by treatment with proteasome inhibitors or by mutations in the RING domain (Anderson et al., 2006; Fletcher et al., 2015; Kutluay et al., 2013; Roa et al., 2012; Wu et al., 2006). These treatments do not block TRIM5 binding, but presumably do interfere with ubiquitin-mediated signaling events. Thus, although TRIM5 binding can destabilize helical CA tubes in vitro (Black and Aiken, 2010; Zhao et al., 2011), capsid dissociation and inhibition of reverse transcription appear to require ubiquitin-dependent signaling in cells (Campbell et al., 2015; Fletcher et al., 2015). Capsid binding can activate TRIM5 ubiquitin E3 ligase activity in vitro (Pertel et al., 2011), and the structure of the hexagonal TRIM5 lattice suggests how this could occur. Recent structural studies of the RING domains from TRIM37 (PDB ID: 3LRQ) and TRIM5α (PDB ID: 4TKP) (Yudina et al., 2015) have demonstrated that the RING domains function as dimers. However, the antiparallel structure of the TRIM5 coiled-coil precludes close contact of the two RING domains within a single TRIM5 dimer (Goldstone et al., 2014; Sanchez et al., 2014). Thus, RING domains from multiple different TRIM5 dimers apparently must come together to transfer ubiquitin. Our lattice structures reveal such associations of three TRIM5 RING domains at local three-fold axes in the hexagonal net (Figure 7D). This suggests that two of the RING domains may join to form an active dimer and that the third 'orphan' RING domain could then be used as a substrate for autoubiquitylation. This idea is supported by 1) recent studies that demonstrate that autoubiquitylation occurs in vitro and in cells and that Lys45 and Lys50 within the RING domain of rhesus TRIM5α are preferentially ubiquitylated (Fletcher et al., 2015), and 2) the accompanying structural studies (Wagner et al., 2016) of a truncated rhesus TRIM5α protein comprising a B-box 2 and the truncated coiled-coil and L2 linker domains (termed 'mini-TRIM'), which reveal that the B-box 2 domains can mediate trimerization. Hence, in addition to enhancing binding avidity, formation of hexagonal TRIM5 lattices may also activate the ubiquitin signaling cascade that ultimately results in capsid dissociation and inhibition of reverse transcription.
HEK 293T and HeLa cells were grown at 37°C with 5% CO2 in DMEM media (Gibco) supplemented with 10% heat-inactivated fetal calf serum and 2 mM L-glutamine. Plasmid constructs for virus production and for expressing TRIM5, CA, and OSF-CypA in mammalian, insect and bacterial cells were created by standard cloning and mutagenesis methods (details available upon request). The plasmids used in this study are summarized in Supplementary file 1A. All plasmids have been submitted to the Addgene (https://www.addgene.org/) and DNASU (https://dnasu.org/DNASU/) public repository.
TRIM5-21R and TRIM5-21RΔSPRY proteins were expressed, purified and assembled into 2D crystals as previously described (Ganser-Pornillos et al., 2011), except that the TRIM5-21R1-300 assembly was promoted by addition of an equal volume of 0.1 M sodium chloride, 0.1 M bicine, pH 9.0, 20% polyethylene glycol monomethyl ether 5000 to the concentrated protein solution.
To prepare samples for ECT, 3 µl of polymerized lattice was mixed with 10 nm Au fiducials and applied to a 2/2 holey carbon-coated Cu EM grid (Quantifoil) and transferred with forceps to the environment chamber of a Vitrobot Mark III (FEI) maintained at 25°C and 80% relative humidity. Excess liquid was manually blotted from the grids on one side before plunging into liquid ethane. Cryo-preserved grids were imaged in a 300 kV FEI G2 Polara equipped with a field emission gun and energy filter (slit width set at 20 eV), and fitted with a K2 Summit direct detector. Tilt-series were collected over a series of angles ranging from −60° to +60° using a step size of 1°; 22,500x magnification (effective pixel size of raw data is 5 Å), a total dose of 150 e/Å2, and a defocus of -6 μm. UCSF Tomo (Zheng et al., 2007) was used to collect the tilt series, and 3D reconstructions were carried out using a weighted back-projection algorithm tracking 10 nm fiducials in IMOD (Kremer et al., 1996). The pixel size in the final reconstruction was 20 Å.
Subtomogram averages of the TRIM5-21R and TRIM5-21RΔSPRY lattices were generated using PEET in IMOD (Nicastro et al., 2006). 153 and 75 vertices were selected in the TRIM5-21R and TRIM5-21RΔSPRY 2D lattices, respectively, and a volume of 60 nm x 60 nm x 20 nm (x,y,z) centered on the refined positions of the selected vertices was used to generate the averaged volume. To localize the SPRY domain in the full-length TRIM5-21R lattice, the density values of the averaged lattice volumes were rescaled to reflect a mean value of zero and standard deviation of 10. The volumes were then aligned in Chimera (Pettersen et al., 2004), and the TRIM5-21RΔSPRY density values were subtracted from the TRIM5-21R volume. The resulting density difference map was contoured and displayed at 3 sigma above the mean.
An important difference between the TRIM5-21R and TRIM5-21RΔSPRY assemblies is that in the absence of the SPRY domains, multiple hexagonal lattices stacked on 'top' of one another close together, laterally offset by a quarter, half, or three-quarters the distance across a hexagon. Thus in projections through 3D subtomogram averages, like those shown in the bottom middle panels of Figure 1C and D, all of these other offset lattices appear, but less prominently than the main lattice. Due to the special pattern of the offsets (one quarter, half, and three-quarters across) and the hexagonal geometry, their projections all intersect at the center of the arms of the main lattice, causing that position to appear especially dark and large. Furthermore, the four-helix bundle of both TRIM5-21R and TRIM5-21RΔSPRY also contributed to the observed densities in the center of the hexagon edges. Figure 1E shows, however, a thin slice through the 3D difference map containing only the main hexagonal lattice, revealing the position of the SPRY domain without interference from the lattices above and below.
To quantify the variability in the TRIM5-21R hexagonal lattice, the refined positions of each vertex were used to calculate: 1) the distance between neighboring vertices, and 2) the average angle of hexamer edges extending from the three-fold vertices. These values were entered into the imodsetvalues program in IMOD and a pseudo-colored model was generated to reflect length (colored lines) and average angles (colored spheres) (Figure 1F).
HEK 293T cells were used to generate lentiviral vectors for transduction of HeLa cells for expression of TRIM5 proteins with a C-terminal Flag One-STrEP tag. pCMV-ΔR8.2 (structural genes) (Naldini et al., 1996), pCMV-VSVG (envelope) (Sandrin et al., 2002; Yee et al., 1994), and CSII-IDR2 (contains a packaging signal and genes for TRIM5 and DsRed) were co-transfected in 293T cells. After 3 days, virion-containing media was removed from the cells, passed through a 0.45 μm filter (Nalgene SFCA syringe filters), layered on top of a 20% sucrose cushion in HS buffer (10 mM HEPES pH 7.2 and 140 mM NaCl) and spun in an Optima L-90K Ultracentrifuge at 96,281 g (Beckman SW32 Ti rotor) for 2 hr at 4°C. Virion-containing pellets were resuspended in HS buffer, aliquoted, and frozen at -80°C. Thawed aliquots were titrated on HeLa cells to determine viral titers by monitoring the number of DsRed positive cells using fluorescence-activated cell sorting (FACS).
HeLa cells (1 x 105 cells per well of 6-well plate) were transduced with lentiviral vectors expressing different TRIM5 proteins at an multiplicity of infection (MOI) of 1. Three days after transduction, cells were split and reseeded at 5 x 104 cells per well of a 24-well plate and infected with increasing amounts of HIV-GFP per well. The remaining cells were used for western blot analysis to determine TRIM5 expression levels. Three days after infection with HIV-GFP, cells were trypsinized, and GFP and DsRed positive cells were counted using FACS. Only DsRed positive cells (which also expressed TRIM5) were used for statistical analysis of HIV-GFP restriction.
Recombinant baculoviruses expressing TRIM5 proteins with either N-terminal One-STrEP-FLAG (OSF) or C-terminal FLAG-One-STrEP (FOS) HRV14-3C protease-cleavable tags were generated using the Bac-to-Bac baculovirus expression system (Thermo Fisher Scientific). Suspension SF9 insect cells (2 L at 2 x 106 cells/ml) grown in ESF-921 medium (Expression Systems) were infected with recombinant baculoviruses at an MOI of 10, and harvested by centrifugation 48 hr later. All purification steps were performed at 4°C. Cell pellets were resuspended in 5 times the pellet volume of lysis buffer (70 mM N-Cyclohexyl-2-aminoethanesulfonic acid (CHES), 100 mM NDSB-256, 1.5% Triton X-100, 100 nM ZnCl2, 1 mM Tris(2-carboxyethyl)phosphine (TCEP), 0.7% protease inhibitor cocktail (v/v, Sigma), 100 U avidin, pH 10.0) and lysed by freeze-thaw and sonication (3 x 30 s on ice; Branson sonifier 450, 50% duty cycle, 50% output). Cell lysates were clarified by ultracentrifugation at 184,000 g (Beckman Ti 50.2 rotor) for 1 hr. The supernatants were filtered (0.45 μm) and loaded onto a 5 ml StrepTrap HP column (GE Healthcare) pre-equilibrated in binding buffer (20 mM CHES, 100 nM ZnCl2, 1 mM TCEP, pH 10.0). The column was washed with 20 column volumes (CV) of binding buffer supplemented with 1 M NaCl and 100 U avidin (VWR), followed by 5 CV of binding buffer. The protein was eluted in 6 CV binding buffer supplemented with 2.5 mM D-desthiobiotin (Sigma). The eluate was diluted to 0.3 mg/ml protein in binding buffer to minimize protein loss due to self-assembly, and dialyzed overnight against 1 L cleavage buffer (25 mM Tris, 1 mM TCEP, pH 8.0) supplemented with ~ 1:100 (by mass, enzyme:substrate) His6-HRV14-3C and His6-Usp2 enzymes to remove the OSF tag and any linked ubiquitin added during insect cell expression. TRIM5αhu and TRIMCyp formed soluble/insoluble aggregates at pH 8.0 and were therefore dialyzed against 20 mM CHES, 1 mM TCEP, pH 9.0. Most TRIM5 proteins were sensitive to non-specific internal proteolysis by HRV14-3C protease. We therefore used the minimal amount (which differed between constructs) required to completely cleave the OSF tag overnight. When cleavage was complete, the pH of the protein solution was adjusted to 10 by direct addition of 1 M CHES, pH 10.0, to a final concentration of 100 mM. The sample was applied onto two tandem 5 ml HiTrap Q HP columns (GE Healthcare) pre-equilibrated with binding buffer, and eluted with a 12 CV linear NaCl gradient (0–1 M) in binding buffer. Fractions containing TRIM5 proteins were pooled, dialyzed against 1 L binding buffer for at least 4 hr, loaded onto a HiLoad 16/600 Superdex 200 gel filtration column (GE Healthcare) pre-equilibrated with binding buffer, and eluted in 1 CV of binding buffer. Fractions corresponding to TRIM5 dimers were pooled and concentrated to 1 mg/ml using a Vivaspin 20 concentrator (10,000 MWCO PES for TRIM5αAGMpygΔSPRY and 30,000 MWCO PES for full-length TRIM5α and TRIMCyp, Sartorius Stedim). Average yields were 4 mg (1.3–9.6 mg) per liter insect cell culture and protein identities were confirmed by electrospray ionization mass spectrometry (ESI-MS) (see Supplementary file 1B).
Freshly purified TRIM5αAGMpyg protein was concentrated to 1–3 mg/ml and assembled by incubating at 23°C for 1 hr and then at 4°C for 1–2 days. For EM analyses, 5 μl sample aliquots were incubated on carbon-coated EM grids for 5 min. The grids were washed by placing each grid on a single 40 μL drop of 0.1 M KCl for 3 min, briefly blotted, and then stained on a single 20 μL drop of 2% uranyl acetate for an additional 3 min.
Unlike TRIM5αAGMpyg, TRIMCyp did not spontaneously assemble into hexagonal lattices following concentration. However, crystals were occasionally observed when an equal volume of 0.01 M cobalt chloride hexahydrate, 0.1 M MES monohydrate pH 6.5, and 1.8 M ammonium sulfate was added to freshly concentrated protein at ~1 mg/ml.
As previously described (Ganser-Pornillos et al., 2011), 2-dimensional crystals composed of cross-linked, hexagonal HIV-1 CA were prepared by incubating 232 μM CA-NCA14C/E45C/W184A with a small 25-TG oligo (143 μM). TRIM5 proteins were then added in 1- to 10- fold molar excess, and the pH was immediately adjusted to 9.0 by direct addition of Tris buffer to a final concentration of 100 mM. Samples were incubated for 1–96 hr, applied to carbon-coated EM grids for 60 s, washed and stained as described above, and visualized by EM. Ten fold lower amounts were sufficient for TRIMCypK283D,Q287D templated assembly.
2L of E.coli Rosetta (λDE3) pLysS cells (Stratagene) carrying the HIV-1 CA A14C/E45C/A92E expression construct were grown to an OD600 nm of 0.6 in LB medium at 37°C, cooled to 19°C and protein expression was induced with 1 mM isopropyl-β-D-thiogalactopyranoside (IPTG) followed by overnight incubation with shaking. HIV-1 CA proteins were purified and assembled into tubes as previously described (Pornillos et al., 2010), except that a higher concentration of dithiothreitol (DTT, 100 mM) was used during protein purification to improve solubility and increase yields. All purification steps were performed at 4°C. Cells were lysed as described above, and proteins were purified from clarified lysates by ammonium sulfate precipitation, dialyzed against 25 mM MOPS, 100 mM DTT, pH 6.5, and loaded onto a 5 ml HiTrap Q HP column (GE Healthcare) pre-equilibrated with the same buffer. The flow-through was applied onto a 5 ml Hi-Load SP Sepharose High Performance column (GE Lifesciences) and eluted with a linear NaCl gradient (0–500 mM) in the same buffer. Fractions containing CA proteins were pooled and dialyzed overnight against storage buffer (20 mM Tris, 40 mM NaCl and 100 mM DTT, pH 8.0). The CA proteins were then concentrated to a stock of 3 mg/ml using a Vivaspin 20 concentrator (10,000 MWCO PES, Sartorius Stedim) and stored at -80°C. Yields were ~20 mg per liter of culture, and the protein identity was confirmed by ESI-MS (MWexp=25,667 Da, MWcalc=25,667 Da).
OSF-CypA was expressed in 2L of E. coli Rosetta (λDE3) pLysS cells (Stratagene) grown in ZYP-5052 media using an autoinduction system (Studier, 2005). Cells were lysed on ice by sonication in lysis buffer (50 mM Tris, pH 8.0, 50 mM NaCl, 10 mM β-mercaptoethanol (β-ME), 0.2% (w/v) deoxycholate, 2.5 nmol avidin, 20 μg/ml DNase 1) supplemented with protease inhibitors (20 μg/ml PMSF, 0.4 μg/ml pepstatin, 0.8 μg/ml leupeptin and 1.6 μg/ml aprotinin). All purification steps were performed at 4°C. Cell lysates were clarified by centrifugation at 17,649 g (Beckman JA-20 rotor) for 45 min, filtered (0.45 μm) and loaded onto two 5 ml tandem StrepTrap HP columns (GE Healthcare) pre-equilibrated in binding buffer (100 mM Tris, 150 mM NaCl, 10 mM β-ME, pH 8.0). The column was washed with 10 CV of binding buffer, and OSF-CypA was eluted in 3 CV of the same buffer supplemented with 2.5 mM D-desthiobiotin. The protein was dialyzed against Q buffer (50 mM Tris, 50 mM NaCl, 10 mM β-ME, pH 8.0) and loaded onto two tandem 5 ml HiTrap HP Q-Sepharose anion exchange columns (GE Healthcare) pre-equilbrated in the same buffer. The OSF-CypA-containing flowthrough was collected and concentrated using Amicon Stirred Ultrafiltration Cells (Millipore). OSF-CypA (>99% pure) was obtained in high yields (∼100 mg per liter bacterial culture), and its identity was confirmed by ESI-MS (MWexp =23,806 Da, MWcalc, -Met1=23,807 Da).
CAA14C/E45C/A92E tubes were assembled at 1 mg/ml by dialysis against dialysis buffer (20 mM Tris, pH 8.0, 1 M NaCl, and 100 mM DTT) at 4°C overnight, followed by dialysis against the same buffer lacking DTT overnight to allow the formation of disulfide crosslinks within the CA hexamers. Disulfide-crosslinked CA tubes were then dialyzed against 20 mM Tris, 40 mM NaCl, pH 8.0 and stored at 4°C.
TRIM5-CA tube binding experiments were performed as previously described, with minor modifications (Ganser-Pornillos et al., 2011; Langelier et al., 2008; Stremlau et al., 2006). Recombinant TRIM5α and TRIMCyp proteins (0.25 μM) were incubated alone or with CAA14C/E45C/A92E tubes (2 μM) in binding buffer (20 mM HEPES, 25 mM NaCl, 1 mM TCEP, pH 7.2) in a final volume of 225 μl at 4°C for 1 hr. Aliquots (10 μl) of the incubation mixtures were mixed with 2X SDS-PAGE sample loading buffer for assessment of protein amounts in the inputs. Aliquots (200 μl) of the mixtures were layered onto a 60% (w/v) sucrose/PBS cushion (4 ml, prepared in binding buffer lacking TCEP) and subjected to centrifugation at 108,109 g (Beckman SW50.1 rotor) for 30 min at 4°C to separate free TRIM5α or TRIMCyp and unassembled CA proteins from CA tube-bound TRIM5 proteins and pelletable CA tubes. Following centrifugation, aliquots (45 μl) of supernatant (500 μl in total) were mixed with 4X SDS-PAGE sample loading buffer, and the pellets were resuspended in 25 μl 1X SDS-PAGE sample loading buffer. The TRIM5 and CA proteins in the input (3%), supernatant (3%) and pellet (30%) were separated by 12% SDS-PAGE, electrophoretically transferred onto nitrocelluose membranes (Bio-Rad) and analyzed by western blotting with mouse anti-TRIM5α monoclonal (clone 5D5-1-1), NIH AIDS Research and Reference Reagent Program, 1:000 dilution) and rabbit anti-HIV-1 CA polyclonal (made in-house UT 416, 1:3000 dilution) antibodies. Secondary IRDye800cw-conjugated donkey anti-mouse IgG (1:10,000, Rockland) or IRDye700DX-conjugated donkey anti-rabbit IgG (1:10,000, Rockland) antibodies were visualized using an Odyssey infrared imaging system (LI-COR Bioscience).
3.5 μl sample solutions of undecorated or TRIM5-decorated CA tubes were spread onto the carbon side of freshly glow-discharged, Formvar/Carbon-coated, 200-mesh copper grids (Electron Microscopy Sciences). The samples were incubated for 4 min, rinsed briefly by flotation on a drop of 100 mM KCl, blotted dry, stained for 2 min in filtered, saturated uranyl acetate (or 1 min in 1% phosphotungstate), blotted dry, and allowed to air dry. Samples were viewed on a JEOL JEM-1400 Plus transmission electron microscope operated at 120 kV accelerating voltage, and images were acquired as Gatan Digital Micrograph 3 (DM3) files with a Gatan Ultrascan CCD camera or on a Hitachi 7100 TEM at 75 kV accelerating voltage with a Gatan ORIUS CCD camera, and converted into JPEG images using ImageJ software (NIH Bethesda, MD, USA).
TRIM5-CA tube complexes were prepared by incubating TRIM5α or TRIMCypK283D,Q287D proteins with hyperstable CA tubes in 50 mM Tris, 8 mM NaCl buffer at 4°C. Decoration conditions were surveyed at a constant CA concentration (7.5 μM) over a range of TRIM5 concentrations (0.5–22.5 μM, corresponding to molar ratios of TRIM5 to CA of 1:16, 1:8, 1:6, 1:3, 1:1 and 3:1), pH values (8.0 and 9.0) and incubation times (4–92 hr). Conditions that produced the best TRIM5 decoration and minimal CA-free TRIM5 self-assemblies were determined by negative stain TEM imaging on a JEOL JEM-1400 Plus transmission electron microscope as described above. Image contrast was uniformly adjusted to enhance the decoration patterns of TRIM5 proteins on CA tubes using Adobe Photoshop CS5. The spacings of hexagonal TRIM5 rings were measured using ImageJ. Human TRIM5α and TRIM5αR332P tended to aggregate in all incubation conditions tested. These aggregates sometimes associated with CA tubes, but could be readily distinguished from ring-like decorated tubes. For scoring, images were judged blind by two independent colleagues.
TRIM5α-CA tube complexes were prepared by incubating 1 μM TRIM5αAGMpyg proteins with 8 μM hyperstable CA tubes in 50 mM Tris, pH 8.0, and 8.2 mM NaCl buffer at 4°C for 32 hr. Quick-freeze deep-etch EM was performed according to published protocols (Heuser, 1980). Briefly, a 3 μl droplet of TRIM5αAGMpyg decorated tubes was placed onto an acid cleaned, air dried 3x3 mm coverglass and covered by a 0.05 mm thick, 3 mm diameter wafer of sapphire on top. The sample was then mounted onto the freezing stage of a Heuser designed 'Slam Freezer' and frozen by forceful impact against a pure copper block, cooled to 4°K with liquid helium. Frozen samples were transferred to a liquid-nitrogen-cooled Balzers 400 vacuum evaporator. Freeze fracture occurred by popping off the sapphire top at -104°C under vacuum. Samples were etched for 210 s at −104°C and rotary replicated with ~3 nm platinum deposited from a 15° angle above the horizontal, followed by an immediate ~10 nm stabilization film of pure carbon deposited from an 85° angle. Replicas were floated onto a dish of concentrated hydrofluoric acid and transferred through 3 rinses of distilled H2O containing a loopful of Photo-flo. Replicas were picked up on formvar coated copper grids, and imaged on a JEOL 1400 microscope with attached AMT digital camera.
Coassembly experiments were performed by incubating HIV-1 CA (650 μM) alone or with TRIM5αAGMpyg (1–15 μM) in assembly buffer (20 mM Tris, pH 8.0, 50 mM NaCl) at 37°C for 2–3 hr, followed by a 2 hr incubation at room temperature. Following incubation, a 3.5 μL aliquot of the assembly reaction was incubated on carbon-coated EM grids (Electron Microscopy Sciences) for 1–2 min. Grids were then placed directly onto a 20 μL drop of 0.1 M KCl for 2 min, blotted and moved to a 20 μL drop of 2% uranyl acetate for 2 min, blotted, and air dried. Samples were imaged on either a Tecnai T12 or a Tecnai F20 microsope operating at 120 kV.
HEK 293T cells (29 x 10 cm plates) were co-transfected (polyethylenimine, PEI, Polysciences) at 70–80% confluency with pLOX-GFP (5 μg DNA/plate) (Salmon et al., 2000) and pCMV-ΔR8.2 vectors (5 μg DNA/plate) (Naldini et al., 1996) that expressed HIV structural proteins encoding wild type or mutant CA sequences (A14C/E45C or A14C/E45C/A92E). 40 hr later, virion-containing media was pooled, filtered (0.45 μm) and pelleted by ultracentrifugation through a 4 ml, 20% sucrose/PBS cushion in 25 x 89 mm polyallomer centrifuge tubes (Beckman Coulter) at 96,281 g (Beckman SW32 Ti rotor) for 2 hr at 4°C. Subsequent core purification steps were performed at 4°C.
Wild type and hyperstable HIV-1 A14C/E45C cores were isolated from virions using an adaptation of a sucrose-gradient, spin-through method (Kotov et al., 1999; Langelier et al., 2008). Virion pellets were resuspended with 2.4 ml ST buffer (20 mM Tris, 75 mM NaCl, pH 7.4). 6 x 11.5 ml 30–70% (w/v) continuous sucrose gradients in ST buffer were made in 14 x 89 mm polyallomer centrifuge tubes (Beckman Coulter) using a gradient maker (Biocomp). The gradients were overlaid with a 300 μl 15% (w/v) sucrose cushion in ST buffer containing 0.5% Triton X-100 (to delipidate the virions as they migrated through the cushion) and then with a 300 μl non-detergent barrier layer (7.5% sucrose in ST buffer), which protected virions from premature detergent exposure. Concentrated virions were applied to the top of the gradient and subjected to centrifugation at 151,263 g (Beckman SW41 Ti rotor) for 16 hr. Twelve 1 ml fractions were collected from the bottom of each tube, and the density of each fraction was determined from the refractive index using a digital refractometer (Leica). The CA content in each fraction was analyzed by western blotting using rabbit anti-HIV-1 CA polyclonal antibodies (made in-house, UT 416, 1:3000 dilution). Fractions 10–12 (density = 1.22–1.27 g/ml), which contained intact HIV-1 cores, were pooled, diluted with ST buffer, and subjected to ultracentrifugation at 151,263 g (Beckman SW41 Ti rotor) for 2 hr. The pelleted cores were resuspended in 240 μl ST buffer, and recovered yields were quantified as described below.
2.4 ml of concentrated virions in PBS were mixed gently with an equal volume of lysis buffer (1% Triton X-100, 100 mM Tris, 2M NaCl, pH 8.0) in the presence of 35 μM OSF-CypA and incubated for 3 min at 23°C. Subsequent core purification steps were performed at 4°C. 8 mg of MagStrep'type2HC' beads (IBA GmbH) were added to the lysed virions and mixed gently by inversion for 7 min to allow OSF-CypA to bind the membrane-stripped cores. The sample was then placed on a PolyATtract system 1000 magnet separation stand (Promega) for 3 min, and the supernatant (‘Flow-through’ in Figure 5—figure supplement 1E) was removed. Captured cores were washed 10 times with high salt buffer (50 mM Tris, 1 M NaCl, pH 8.0) to remove unbound CA proteins and contaminating vesicles, and the final wash sample was saved for western blot analysis (‘Wash’ in Figure 5—figure supplement 1E). Cores were eluted in 150 μl elution buffer (50 mM Tris, 75 mM NaCl, pH 8.0) supplemented with 40 μM Cyclosporine A (Sigma-Aldrich) and incubated with inversion for 40 min. The sample was subjected to brief centrifugation in a tabletop ultracentrifuge at 1000 g for 5 s and placed on a Magnesphere Technology Magnetic Separation Stand (Promega) for 5 min. The supernatant containing the purified cores (‘Eluate’ in Figure 5—figure supplement 1E) was collected and used in the experiments shown in Figures 5, 6, 7, Figure 5—figure supplement 1, and Figure 7—figure supplement 1, 2 and 3. Beads before and after CsA elution were also saved for western blot analyses (Figure 5—figure supplement 1E).
Virion inputs and core yields were quantified by western blot densitometry against a standard curve of recombinant CA proteins for reference. The recovery of cores from virions was calculated by normalizing core yields of CA to corresponding virion CA inputs, which were set to 100%. As illustrated in Figure 5, disulfide crosslinks apparently stabilized the HIV-1 cores, resulting in a ~4 fold increase in the core recovery (0.8 ± 1%; core yields: 0.6 ± 0.5 μg CA; virus input: 100 ± 80 μg CA, n = 10) compared to wild type cores (0.2 ± 0.1%; core yields: 0.08 ± 0.05 μg CA; virus input: 40 ± 30 μg CA, n = 7). The affinity purification method consistently raised the yield of hyperstable HIV-1 A14C/E45C cores by an additional ~4 fold (3 ± 2%; core yields: 1 ± 0.6 μg CA; virus input: 40 ± 8 μg CA, n = 3) vs. the sucrose-gradient, spin-through method. Core recovery was not affected by the A92E mutation (3 ± 1%; core yields: 3 ± 1 μg CA; virus input: 100 ± 60 μg CA, n = 7).
Discrete particles were imaged by negative stain EM and scored as 'tubular' if their edges appeared parallel, as 'spherical' if they were spherical or elliptical, and as 'conical' if they lacked the above properties. The final class included conical, triangular, bullet-shaped, and coffin-shaped cores.
To examine disulfide crosslinking within purified cores, sucrose gradient fractions 7–9 and 10–12 were pooled separately, mixed with SDS-PAGE sample loading buffer lacking β-ME (or containing the concentrations designated in Figure 5C), treated with 31.25 μM methyl methanethiosulfonate (Pierce Biotechnology), heated at 95°C for 10 min, and electrophoresis was performed on 4–15% gradient SDS polyacrylamide gels (Bio-Rad) and analyzed by western blotting.
Purified cores were denatured in SDS-PAGE sample loading buffer, resolved on 4–15% gradient SDS polyacrylamide gels (Bio-Rad) and stained using SilverQuest silver staining kit (Thermo Fisher Scientific).
Recombinant TRIM5αAGMpyg and TRIM5αcpz proteins (0.5 μM) were incubated at 4°C for 1 hr alone or with hyperstable HIV-1 cores (0.5–1 μM) in binding buffer (40 mM HEPES, 50 mM NaCl, 1 mM TCEP, pH 7.2) in a final volume of 75 μl. TRIM5αrh (0.25 μM) was incubated alone or with hyperstable cores under slightly more alkaline conditions (40 mM Tris, 50 mM NaCl, 1 mM TCEP, pH 8.0) to minimize untemplated assembly of TRIM5α during sedimentation. Human TRIM5α proteins were not used in these assays because they tended to aggregate and pellet, even in the absence of HIV-1 cores. TRIMCyp was also not used owing to low levels of residual cyclosporine A in the core preparations. Aliquots (5 μl) of the mixtures were mixed with 2X SDS-PAGE sample loading buffer (‘Input’ in Figure 6). The mixtures were layered onto a 30% (w/v) sucrose cushion (4 ml, prepared in binding buffer lacking TCEP) and subjected to centrifugation at 149,632 g (Beckman SW50.1 rotor) for 2.5 hr to separate free TRIM5α and unassembled CA proteins from capsid-bound TRIM5 proteins and pelletable cores. Following centrifugation, aliquots (45 μl) of supernatant (500 μl in total) were mixed with 4X SDS-PAGE sample loading buffer, and the pellets were resuspended in 25 μl 1X SDS-PAGE sample loading buffer. The TRIM5 and CA proteins in the input (2%), supernatant (2%) and pellet (30%) were separated by 12% SDS-PAGE. The integrated intensities of protein bands on the western blots were measured using the Odyssey software (LI-COR Bioscience). The molar ratios of TRIM5αAGMpyg to CA in the pellets were estimated from standard curves constructed from known amounts of TRIM5αAGMpyg and CA loaded on the same gel.
TRIM5α-core complexes were prepared by incubating TRIM5αrh with affinity-purified hyperstable HIV-1 cores in 50 mM HEPES (pH 8.0) or CHES (pH 9.0), 0.1 mM TCEP buffer at 4°C. Decoration conditions were surveyed over a range of TRIM5αrh concentrations (0.25–2 μM), NaCl concentrations (50 or 200 mM), and incubation times (2–92 hr). Conditions that gave the best TRIM5α decoration on HIV-1 cores with minimal TRIM5α self-assemblies were determined by negative stain TEM imaging on a JEOL JEM-1400 Plus transmission electron microscope as described above. Clear decoration was difficult to discern in the majority of the TRIM5α-incubated cores, likely because TRIM5α decorations were obscured by uranyl acetate staining of the underlying viral ribonucleoprotein complexes, and cores with clear external TRIM5α decoration patterns were observed on only ~5% of 907 core particles examined. Cores incubated in the absence of TRIM5α proteins and stained under the same conditions never showed equivalent decorations.
TRIM5α-decorated CA tubes were prepared by incubating 1.5 μM TRIM5αAGMpyg with 695 μM wild type CA in 90 μl of assembly buffer (20 mM HEPES, 50 mM NaCl, pH 8.0) at 37°C for 2 hr, followed by a 2 hr incubation at room temperature. TRIM5α-decorated HIV-1 cores were prepared by incubating 0.5 μM TRIM5αAGMpyg with 0.6 μM CA equivalents of hyperstable HIV-1 cores in 75 μl of binding buffer (40 mM HEPES, 50 mM NaCl, 1 mM TCEP, pH 7.2) at 4°C for 1 hr, a condition that produced saturation binding in the co-sedimentation assay (data not shown). TRIM5α-tube complexes, cores, or TRIM5α-core complexes were mixed with BSA-coated colloidal gold particles (10 nm, SPI Supplies), which served as fiducials required for aligning the tilt stacked images. For crosslinked complexes, the pH of the samples was adjusted to 8.0 by adding 1/20th the sample volume of 1 M HEPES, pH 8.0, and the samples were incubated with 1 mM Sulfo-EGS (Pierce Biotechnology) at 23°C for 10 min in 88 μl total reaction volume. The cross-linking reaction was quenched by direct addition of 1 M Tris, pH 7.4, to a final concentration of 50 mM, followed by a 15 min incubation at 23°C. This treatment crosslinked ~87% and ~76% of the TRIM5αAGMpyg and CA subunits of TRIM5-core complexes, respectively, as analyzed by SDS-PAGE and western blotting (data not shown). Samples (3.5 µl) were placed on the carbon side of freshly glow-discharged Quantifoil R2/2, 300 mesh holey carbon grids (SPI Supplies) for 1 min, thinned by automatic blotting using a Vitrobot Mark I (FEI) (-1.5 mm offset, 6–8 s, with filter papers from both sides at 80–85% relative humidity) and vitrified by plunge-freezing into liquid ethane. The cryo-grid was transferred to the microscope using a cryo-transfer holder.
Images were collected using a 300 kV FEI G2 Polara transmission electron microscope equipped with an energy filter (slit width 20 eV; Gatan) and a 4k x 4k K2 Summit using the direct electron counting mode (Gatan). Pixels on the detector represented 0.26 nm (41,000x) at the specimen level. The tilt series were recorded from -60° to +60° with an increment of 1° and 4 μm underfocus. The cumulative dose of a tilt-series was 80–100 e-/Å2. UCSF Tomo (Zheng et al., 2007) was used for automatic acquisition of the tilt series and 2D projection images. The tilt series was aligned and binned by 4 into 1k x 1k using the IMOD software package (Kremer et al., 1996), and 3D reconstructions were calculated using the simultaneous reconstruction technique (SIRT) implemented in the TOMO3D software package (Agulleiro and Fernandez, 2011), or weighted back projection using IMOD. Noise reduction was performed using the non-linear anisotropic diffusion (NAD) method in IMOD (Kremer et al., 1996), typically using a K value of 0.03–0.04 with 10 iterations.
Segmentation and isosurface rendering were performed in Amira (FEI). The outer boundary of the HIV-1 tube or core was first manually identified, and a material mask was generated inside the boundary. A second region of interest surrounding the tube or core that typically extended 9 nm from the exterior surface was generated (densities inside this region correspond to TRIM5α protein). The area inside the second region was segmented and an isosurface generated for the densities inside. Islands containing six voxels or fewer in 3D were deleted for the segmented cores, and four voxels or fewer were deleted for the co-assembled tube. The exterior layer of the CA protein within the HIV-1 tube or core of the first material was also segmented using a similar threshold value, and an isosurface was generated. Movie image sequences were generated in JPEG format in Amira (FEI) and converted into movies using QuickTime Player 7. Photoshop CS6 (Adobe) was then used to produce the final versions of the movies.
Crystal structures of the B-box 2 trimer (PDB 5EIA)(Wagner et al., 2016) and B-box 2/coiled-coil dimer (PDB 4TN3)(Goldstone et al., 2014) were fitted manually as separate units into the map using UCSF chimera (Pettersen et al., 2004). The trimer structures were initially placed at putative three-fold densities, and then iterative superpositions and manual adjustments were performed to optimize the overlap between the B-box 2 portions of the two source PDB files. No geometric optimization was performed, and the fitting should be treated as a simple proof of principle that the dimensions of the hexagon densities observed in the cryotomograms are compatible with dimensions and interactions observed in the crystal structures.
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Stephen P GoffReviewing Editor; Howard Hughes Medical Institute, Columbia University, United States
In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.
Congratulations: we are very pleased to inform you that your article, "Primate TRIM5 proteins form hexagonal nets on HIV-1 capsids", has been accepted for publication in eLife. The Reviewing Editor for your submission was Stephen Goff and the Senior Editor was Wenhui Li.
All three of our reviewers were enthused about the findings and the paper. They all summarized the salient points and raised only very minor points that can be readily addressed.
Reviewer #1 (General assessment and major comments (Required)):
The authors previously reported that TRIM5 forms a planar, hexagonal lattice and generated a model for how the TRIM5 subdomains are arranged. These experiments were limited in terms of detail and the use of a TRIM5 fusion protein (TRIM5-21R). Here electron cryotomograms (ECT) with full-length and SPRY-deleted TRIM5-21R confirmed the placement of the SPRY domain at the middle of the hexagon edges. The authors then developed a method for generating full-length, authentic TRIM5 proteins and confirmed hexameric lattice formation with 2 TRIM5 orthologues. 2D CA crystals were assembled and dimeric TRIM5 was added under conditions that preclude spontaneous lattice formation by TRIM5. CA-templated assembly was observed with 3 restricting TRIM5s but not with 2 non-restrictive TRIM5s. The purified TRIM5s co-sedimented with recombinant, crosslinked CA tubes. Negative stain and deep-etch EM demonstrated thin nets on the surface of the CA tubes when restrictive TRIM5s were added, but not with controls. The authors made virion cores by detergent extraction and density sedimentation gradient, expertly increasing the core yield with CA A14C/E45C/A92E, and enrichment on cyclophilin A columns. Cores were then incubated with TRIM5 protein and visualized by ECT. Hexagonal nets of TRIM5 were visualized and modeled. This expert body of work shows how restriction factor TRIM5 associates with HIV-1 cores. I have a few minor comments that might help the reader.
Reviewer #1 (Minor Comments):
1) Figure 1C and D: The density difference map in 1E does not seem to match the difference of the representative images shown in the bottom middle panels of 1C and D. It looks like TRIM5-21R-ΔSPRY retains density in the middle of the hexagon edges. Perhaps the authors could clarify this?
2) Concerning TRIM5 purification (subsection “Expression and purification of authentic primate TRIM5α and TRIMCyp proteins”) the authors should acknowledge that another group reported detailed methods for baculo expression and purification of high concentration, authentic TRIM5 from owl monkey (Pertel et al., 2011). Regarding the discussion at the end of the subsection “Reagent development”, this same group also used A14C/E45C stabilized CA cores to stimulate the Ubx E3 activity of purified TRIM5 protein.
3) Figure 3 shows the templated assembly of restrictive TRIM5 on 2D CA lattices. Images with a non-restrictive TRIM5 might help the reader visualize the differences.
4) Figure 4C: The authors state that co-assembly of CA with TRIM5 was more efficient than if TRIM5 was added after CA was preformed into tubes (at the end of the subsection “TRIM5 binding to helical HIV-1 CA tubes”). This statement seems at odds with the histogram in Figure 4C which shows pretty much the same percentages of "Rings on preformed CA tubes" with "Rings on co-assembly".
5) In the subsection “Generation of hyperstable, disulfide-crosslinked HIV-1 core particle”: I don't understand the calculations stated in the text regarding Figure 5A: “[…] a substantial fraction of the CA protein also concentrated at the density expected for native core particles (fractions 10-12, highlighted in pink in Figure 5A, right panel). These "hyperstable" cores were reproducibly recovered in higher yields (0.8 ± 1%) than wild type cores (0.2 ± 0.1%)[…] “Fraction 10 looks to be 25%, not 0.8%?
Reviewer #2 (General assessment and major comments (Required)):
In their manuscript, Li and coworkers report the purification of milligram quantities of TRIM5 restriction factor proteins and structural analysis of complexes of some of them with purified HIV-1 cores and assemblies of recombinant HIV-1 CA protein. The authors also describe a new approach they developed to purify HIV-1 cores from virions. The study represents a significant advance because: (1) TRIM5 proteins have been notoriously difficult to purify, and (2) interactions of TRIM5α with native HIV-1 cores have not been described in the literature. Based on their structural results, the authors conclude that TRIM5 proteins form hexagonal "nets" around the viral capsid resembling those formed spontaneously by the restriction factors. Assuming the technique employed for purifying TRIM5 proteins is robust, this study should greatly facilitate future studies of TRIM5 structure and biochemistry.
I have no significant criticisms.
Reviewer #2 (Minor Comments):
Introduction, third paragraph: the term "viral core replication particle." I don't recall reading this term previously, and it seems like an odd combination of adjectives and nouns.
At the end of the subsection “Structure-based models for TRIM5-21R assembly”: “[…]thereby validating the model[…] “According to Merriam-Webster, the word "validate” implies establishing validity by authoritative affirmation or by factual proof. I suggest replacing this with "supporting."
Reviewer #3 (General assessment and major comments (Required)):
Li et al. report on a fairly comprehensive structural study focused on the nature of the interaction between TRIM5α and incoming retroviral capsid cores. The results to some extent confirm expectations based on highly artificial systems, and greatly extend these through extensive efforts to use bona fide, purified TRIM5α proteins together with capsid preps as close as possible to native structures. This is an important step forward – despite intense focus on TRIM5 and TRIM5-mediated restriction, standard approaches to understanding protein interactions have not been useful. As the authors point out, the methods may also be applicable to the study of the many other known capsid-interacting co-factors in the cell. Another strength of the study is that most results apply to two or more distinct TRIM5 homologs, confirming the generality of the findings. The model is also consistent with known interactions and with the observation that TRIM5-mediated restriction is saturable.
The results also begin to fill in/suggest aspects of mechanism that will certainly drive further work by both structural and cellular laboratories, and this will be a great strength of the paper. Interesting details emerging from the study include the likely intermolecular dimerization of RING domains upon assembly, which suggests a regulatory mechanism that among other things may control the E3 Ub ligase activity in the absence of a target or before sufficient assembly has occurred on the target, and the orientation of the RING domains on the exposed surface of the lattice. Results also indicate that the formation of a hexagonal lattice is a conserved mechanism, and open the door for structural studies to understand both the broad spectrum of retroviruses that can be recognized while also trying to understand how, at the same time, individual retroviruses can "escape" this interaction while maintaining integral capsid functions. It potentially may suggest how other TRIM proteins recognize their respective ligands.
Overall this is an important study and it should have a significant impact on the field.https://doi.org/10.7554/eLife.16269.021
- Mark Yeager
- Barbie K Ganser-Pornillos
- Grant J Jensen
- Wesley I Sundquist
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Deep-etch electron microscopy was performed by Robyn Roth and John Heuser at the Laboratory of Electron Microscopy Sciences, Department of Cell Biology, Washington University School of Medicine. Some of the EM work was conducted at the Molecular Electron Microscopy Core Faciltiy at the University of Virginia, which is supported by the School of Medicine and built with NIH grant (G20-RR31199). We are grateful to Ruth Pumroy for contributing TRIM5 proteins used in our co-assembly assays, to Katherine Ferrell for the gift of His6-Usp2 enzyme, and to members of our laboratories for helpful discussions and critical reading of the manuscript. This work was supported by funds from NIH NIGMS P50 082545 (to MY, BKG-P, GJJ and WIS).
- Stephen P Goff, Reviewing Editor, Howard Hughes Medical Institute, Columbia University, United States
© 2016, Li 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.