Structural basis for channel conduction in the pump-like channelrhodopsin ChRmine

Koichiro Kishi(The University of Tokyo), Yoon Seok Kim(Stanford University), Masahiro Fukuda(The University of Tokyo), Masatoshi Inoue(Stanford University), Tsukasa Kusakizako(The University of Tokyo), Peter Y. Wang(Stanford University), Charu Ramakrishnan(Palo Alto University), Eamon F.X. Byrne(Stanford University), Elina Thadhani(Stanford University), Joseph M. Paggi(Stanford University), Toshiki E. Matsui(The University of Tokyo), Keitaro Yamashita(MRC Laboratory of Molecular Biology), Takashi Nagata(Japan Science and Technology Agency), Masae Konno(Japan Science and Technology Agency), Sean Quirin(Stanford University), Maisie Lo(Stanford University), Tyler Benster(Stanford University), Tomoko Uemura(Kyoto University), Kehong Liu(Kyoto University), Mikihiro Shibata(Kanazawa University), Norimichi Nomura(Kyoto University), So Iwata(Kyoto University), Osamu Nureki(The University of Tokyo), Ron O. Dror(Stanford University), Keiichi Inoue(The University of Tokyo), Karl Deisseroth(Howard Hughes Medical Institute), Hideaki Kato(Japan Science and Technology Agency)
Cell
February 1, 2022
Cited by 148Open Access
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Abstract

ChRmine, a recently discovered pump-like cation-conducting channelrhodopsin, exhibits puzzling properties (large photocurrents, red-shifted spectrum, and extreme light sensitivity) that have created new opportunities in optogenetics. ChRmine and its homologs function as ion channels but, by primary sequence, more closely resemble ion pump rhodopsins; mechanisms for passive channel conduction in this family have remained mysterious. Here, we present the 2.0 Å resolution cryo-EM structure of ChRmine, revealing architectural features atypical for channelrhodopsins: trimeric assembly, a short transmembrane-helix 3, a twisting extracellular-loop 1, large vestibules within the monomer, and an opening at the trimer interface. We applied this structure to design three proteins (rsChRmine and hsChRmine, conferring further red-shifted and high-speed properties, respectively, and frChRmine, combining faster and more red-shifted performance) suitable for fundamental neuroscience opportunities. These results illuminate the conduction and gating of pump-like channelrhodopsins and point the way toward further structure-guided creation of channelrhodopsins for applications across biology.


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