Phylogeny and electrophysiological characterization of identified ACRs.

(A) Phylogenetic relationships among known channelrhodopsin subfamilies with the described ChRs written in black and blue font. The color of the clades indicates ion selectivity: red for ACRs and blue for CCRs. The color of the dots reflects λmax with gray dots corresponding to proteins not yet having their λmax determined. See the extended version of the tree in Figure S1.

(B) Action spectra of identified ACRs. Shown are Gaussian fits, where dots are data points of single measurements.

(C) Strongest activation wavelength (λmax) derived from Gaussian fits of recorded action spectra.

(D) Example current traces of identified ACRs recorded at holding potentials between -80 mV and +40 mV. The gray bar above indicates the illumination period with excitation light of indicated wavelength. The dashed line indicates 0 nA.

(E) Peak photocurrent amplitude at -60 mV holding potential.

(F) Kinetics of the photocurrents returning to the baseline upon light-off (τoff) for tested ACR candidates.

In (C), (E) and (F), black lines are mean ± standard deviation, and circles are data points of single measurements (GpACR1 n = 4, 5, and 5; MsACR1 n = 12, 5, 5; S16-ACR1 n = 4, 7, n.d.; TaraACR1 n = 5, 7, 7; TaraACR2 n = 4, 7, 6; TaraACR3 n = 4, 6, 4 for (C), (E), and (F), respectively). Abbreviation: n.d. means not determined.

Color-tuning of MsACR1.

(A) Structural model of the MsACR1 retinal binding pocket with mutated residues indicated. Residues close to the β-ionone ring are labeled in cyan, and those close to the retinal Schiff base (RSB) are labeled purple. Residue S218, the position of the raACR mutation, is labeled light-red, and the putative counterion D215 is labeled black. Residue side chains and the all-trans-retinal chromophore are shown as sticks except for G123 and G186, where the C? is shown as a sphere. Oxygen is colored in red, nitrogen in blue, and sulfur in yellow.

(B) Example current traces of MsACR1 (blue) and raACR (MsACR1-S218A; light-red). Gray bars above the traces indicate an illumination period with an excitation light of 560 nm. The dashed line indicates 0 nA.

(C) Action spectra of MsACR1 (blue) and raACR (red). Dots are data points of single measurements fitted with a Gaussian function (solid line).

(D) Strongest activation wavelength (λmax) of the indicated single-residue mutants.

(E) Photocurrent amplitudes at -60 mV holding potential (I-60 mv) of the indicated mutants upon excitation with 560 nm light.

(F) Kinetics of the photocurrents returning to the baseline upon light-off (τoff).

In (D-F), black lines are mean ± standard deviation, and circles are data points of single measurements (WT n = 12, 5, and 5, respectively; Mutants n = 3-7).

Silencing of neuronal activity in dissociated hippocampal neurons using MsACR1 and raACR.

(A) Confocal image of a hippocampal neuron ten days after viral transduction expressing MsACR1-mCerulean under control of the hSynapsin1 (hSyn) promoter. The magnified portion of the image of a putative axonal compartment (right side, lower panel) shows a high degree of membrane-targeting of MsACR1. Magnification of the somatodendritic compartment (right side, upper panel) reveals the absence of visible protein aggregation.

(B) Voltage traces of neuronal spiking elicited by a 1-s 250 pA current step illustrating the efficiency of optical silencing at various light intensities (ranging from 200 to 15 x 103 nW/mm2). MsACR1 and raACR were activated for 300 ms with 550 nm light (gray bars) during the current step.

(C) Relative neuronal spiking probability upon optical silencing by MsACR1 (blue) or raACR (red) excited with 550 nm light, as illustrated in (B), at all tested light intensities.

(D) Voltage traces of MsACR1-expressing hippocampal neurons upon current ramps under no light, continuous or 10 Hz pulsed illumination with 550 nm or 635 nm light. Continuous illumination evoked a spike at light on-set (on-set spike).

(E) Spikes elicited by current-ramp injection in the dark (d) or upon continuous or pulsed illumination (i) of 550 nm or 635 nm in neurons expressing MsACR1 (upper row) or raACR (lower row), as shown in (D). Black lines are mean ± standard error, and circles represent single measurements (n = 10-16). Paired two-tailed Wilcoxon or Student’s t-tests were used for MsACR1 and raACR comparisons (p < 0.05).

(F) Temporal precision of neuronal inhibition of MsACR1 (blue) and raACR (red). A paradigm was designed to measure the period after successful suppression of a current-evoked spike in which no new spike can be triggered.

(G) Population data of MsACR1 (blue) and raACR (red) for the experiment are shown in (F).

Inhibition of locomotion in rodents in vivo using MsACR1 and raACR.

(A) Confocal images of coronal brain slices confirm the expression of raACR in the primary motor cortex (M1) and the accurate placement of the optical cannula. A close-up of the injection site confirms homogenous expression in the transduced brain volume with no apparent neuronal degeneration.

(B) Experimental design and stimulation protocol. Animals were allowed to explore the arena for one minute before stimulation at 20 Hz with 635 nm for 2s.

(C) The trajectory of a mouse for bouts with no illumination (black) and periods during light stimulation (red).

(D) Calculated velocity based on pixel deviation during two consecutive frames for periods with illumination (+) and no illumination (Mann-Whitney U=23, P < 0.01).

Maximum-likelihood phylogenetic reconstruction of relationships among known channelrhodopsins.

The sequences chosen for the analysis were taken from the Catalog of Natural Channelrhodopsins (Rozenberg, 2023). Names based on the taxonomic affiliation of the organisms possessing the corresponding genes are indicated for major clades. The clades are colored according to the known or putative ion selectivity of their members: red for ACRs and blue for CCRs. The color of the dots at the edge tips reflects λmax with gray dots corresponding to proteins known to generate photocurrents but having their λmax not yet determined. Dots on the internal branches reflect ultrafast bootstrap values: black for ≥95 and gray for ≥90. The positions of the proteins characterized here are highlighted with labels. HF – heterotrophic flagellates.

Alignment of the rhodopsin domains of the ChRs tested in the current study and chosen reference proteins.

The alignment was constructed using structural information using the crystal structures of BR (PDB: 1AP9), ChR2 (6EID), Chrimson (5ZIH), and GtACR1 (6CSM) and AlphaFold structures for the ChRs studied here. Positions for which MsACR1 mutants were tested are indicated below. The gray bars above the alignment columns indicate transmembrane regions as reported in the OPM database for ChR2.

Light sensitivity and ion selectivity of identified ACRs.

(A) Full action spectra of identified ACRs. Shown are mean ± standard deviation connected by lines.

(B) Light titration of identified ACRs at light intensities between 38 nW/mm2 and 3.2 mW/mm2. Shown are mean ± standard deviation connected by lines.

(C) Half-maximal activation light intensity determined by the logarithmic fit of light titration curves.

(D) Exemplary photocurrent traces of MsACR1 upon activation with 560 nm light at the indicated extracellular Cl- concentration.

(E) Current-Voltage relationship of MsACR1 at indicated extracellular ion conditions.

(F) Reversal potential shifts (DVrev) upon exchange of the extracellular buffer.

In (C) and (E), lines are mean ± standard deviation, and circles are data points of single measurements (n ≥ 3 for all constructs).

The red-light activity of ACRs.

(A) Structural model of the MsACR1. Residue side chains and the all-trans-retinal chromophore are shown as sticks except for G123 and G186, where the C? is shown as a sphere. Oxygen is colored in red, nitrogen in blue, and sulfur in yellow.

(B) Full action spectra of MsACR1 and raACR. Shown are mean ± standard deviation connected by lines.

(C) Photocurrent amplitude of GtACR1, MsACR1, and raACR upon activation with 560 nm and 692 nm light. Lines are mean ± standard deviation, and circles are data points of single measurements (n = 3 for all constructs).

Soma-targeting of MsACR1 and raACR.

(A) Stimulation and illumination paradigms used to assess silencing efficiency for soma-targeted MsACR1 and raACR in dissociated hippocampal neurons.

(B) Spikes elicited by current-ramp injection in no light (d) or upon continuous or pulsed illumination (i) of 550 nm or 635 nm in neurons expressing MsACR1 (upper row) or raACR (lower row), as shown in (A). Black lines are mean ± standard error, and circles represent single measurements (n = 5 - 9). Paired Wilcoxon or Student’s t-tests were used for st-MsACR1 and st-raACR comparisons (p < 0.05).

(C) Wilcoxon-test statistic (one-sided) for the occurrence of a light-evoked spike during continuous and pulsed light stimulation of soma targeted MsACR1 and raACR (n = 5 - 14), p < 0.05.

(D) Wilcoxon-test statistic (one-sided) for the occurrence of a light-evoked spike during pulsed light stimulation (n = 5 - 16), p < 0.05.