Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution

ABSTRACT Cation and anion channelrhodopsins (CCRs and ACRs, respectively) primarily from two algal species, Chlamydomonas reinhardtii and Guillardia theta, have become widely used as optogenetic tools to control cell membrane potential with light. We mined algal and other protist polynucleotide sequ...

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Autores principales: Elena G. Govorunova, Oleg A. Sineshchekov, Hai Li, Yumei Wang, Leonid S. Brown, Alyssa Palmateer, Michael Melkonian, Shifeng Cheng, Eric Carpenter, Jordan Patterson, Gane K.-S. Wong, John L. Spudich
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Publicado: American Society for Microbiology 2021
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spelling oai:doaj.org-article:c53e961158494961a6504a84794cf01b2021-11-10T18:37:52ZCation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution10.1128/mBio.01656-212150-7511https://doaj.org/article/c53e961158494961a6504a84794cf01b2021-08-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01656-21https://doaj.org/toc/2150-7511ABSTRACT Cation and anion channelrhodopsins (CCRs and ACRs, respectively) primarily from two algal species, Chlamydomonas reinhardtii and Guillardia theta, have become widely used as optogenetic tools to control cell membrane potential with light. We mined algal and other protist polynucleotide sequencing projects and metagenomic samples to identify 75 channelrhodopsin homologs from four channelrhodopsin families, including one revealed in dinoflagellates in this study. We carried out electrophysiological analysis of 33 natural channelrhodopsin variants from different phylogenetic lineages and 10 metagenomic homologs in search of sequence determinants of ion selectivity, photocurrent desensitization, and spectral tuning in channelrhodopsins. Our results show that association of a reduced number of glutamates near the conductance path with anion selectivity depends on a wider protein context, because prasinophyte homologs with a glutamate pattern identical to that in cryptophyte ACRs are cation selective. Desensitization is also broadly context dependent, as in one branch of stramenopile ACRs and their metagenomic homologs, its extent roughly correlates with phylogenetic relationship of their sequences. Regarding spectral tuning, we identified two prasinophyte CCRs with red-shifted spectra to 585 nm. They exhibit a third residue pattern in their retinal-binding pockets distinctly different from those of the only two types of red-shifted channelrhodopsins known (i.e., the CCR Chrimson and RubyACRs). In cryptophyte ACRs we identified three specific residue positions in the retinal-binding pocket that define the wavelength of their spectral maxima. Lastly, we found that dinoflagellate rhodopsins with a TCP motif in the third transmembrane helix and a metagenomic homolog exhibit channel activity. IMPORTANCE Channelrhodopsins are widely used in neuroscience and cardiology as research tools and are considered prospective therapeutics, but their natural diversity and mechanisms remain poorly characterized. Genomic and metagenomic sequencing projects are producing an ever-increasing wealth of data, whereas biophysical characterization of the encoded proteins lags behind. In this study, we used manual and automated patch clamp recording of representative members of four channelrhodopsin families, including a family in dinoflagellates that we report in this study. Our results contribute to a better understanding of molecular determinants of ionic selectivity, photocurrent desensitization, and spectral tuning in channelrhodopsins.Elena G. GovorunovaOleg A. SineshchekovHai LiYumei WangLeonid S. BrownAlyssa PalmateerMichael MelkonianShifeng ChengEric CarpenterJordan PattersonGane K.-S. WongJohn L. SpudichAmerican Society for Microbiologyarticlealgaechannelrhodopsinsoptogeneticsphotosensory receptionMicrobiologyQR1-502ENmBio, Vol 12, Iss 4 (2021)
institution DOAJ
collection DOAJ
language EN
topic algae
channelrhodopsins
optogenetics
photosensory reception
Microbiology
QR1-502
spellingShingle algae
channelrhodopsins
optogenetics
photosensory reception
Microbiology
QR1-502
Elena G. Govorunova
Oleg A. Sineshchekov
Hai Li
Yumei Wang
Leonid S. Brown
Alyssa Palmateer
Michael Melkonian
Shifeng Cheng
Eric Carpenter
Jordan Patterson
Gane K.-S. Wong
John L. Spudich
Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution
description ABSTRACT Cation and anion channelrhodopsins (CCRs and ACRs, respectively) primarily from two algal species, Chlamydomonas reinhardtii and Guillardia theta, have become widely used as optogenetic tools to control cell membrane potential with light. We mined algal and other protist polynucleotide sequencing projects and metagenomic samples to identify 75 channelrhodopsin homologs from four channelrhodopsin families, including one revealed in dinoflagellates in this study. We carried out electrophysiological analysis of 33 natural channelrhodopsin variants from different phylogenetic lineages and 10 metagenomic homologs in search of sequence determinants of ion selectivity, photocurrent desensitization, and spectral tuning in channelrhodopsins. Our results show that association of a reduced number of glutamates near the conductance path with anion selectivity depends on a wider protein context, because prasinophyte homologs with a glutamate pattern identical to that in cryptophyte ACRs are cation selective. Desensitization is also broadly context dependent, as in one branch of stramenopile ACRs and their metagenomic homologs, its extent roughly correlates with phylogenetic relationship of their sequences. Regarding spectral tuning, we identified two prasinophyte CCRs with red-shifted spectra to 585 nm. They exhibit a third residue pattern in their retinal-binding pockets distinctly different from those of the only two types of red-shifted channelrhodopsins known (i.e., the CCR Chrimson and RubyACRs). In cryptophyte ACRs we identified three specific residue positions in the retinal-binding pocket that define the wavelength of their spectral maxima. Lastly, we found that dinoflagellate rhodopsins with a TCP motif in the third transmembrane helix and a metagenomic homolog exhibit channel activity. IMPORTANCE Channelrhodopsins are widely used in neuroscience and cardiology as research tools and are considered prospective therapeutics, but their natural diversity and mechanisms remain poorly characterized. Genomic and metagenomic sequencing projects are producing an ever-increasing wealth of data, whereas biophysical characterization of the encoded proteins lags behind. In this study, we used manual and automated patch clamp recording of representative members of four channelrhodopsin families, including a family in dinoflagellates that we report in this study. Our results contribute to a better understanding of molecular determinants of ionic selectivity, photocurrent desensitization, and spectral tuning in channelrhodopsins.
format article
author Elena G. Govorunova
Oleg A. Sineshchekov
Hai Li
Yumei Wang
Leonid S. Brown
Alyssa Palmateer
Michael Melkonian
Shifeng Cheng
Eric Carpenter
Jordan Patterson
Gane K.-S. Wong
John L. Spudich
author_facet Elena G. Govorunova
Oleg A. Sineshchekov
Hai Li
Yumei Wang
Leonid S. Brown
Alyssa Palmateer
Michael Melkonian
Shifeng Cheng
Eric Carpenter
Jordan Patterson
Gane K.-S. Wong
John L. Spudich
author_sort Elena G. Govorunova
title Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution
title_short Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution
title_full Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution
title_fullStr Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution
title_full_unstemmed Cation and Anion Channelrhodopsins: Sequence Motifs and Taxonomic Distribution
title_sort cation and anion channelrhodopsins: sequence motifs and taxonomic distribution
publisher American Society for Microbiology
publishDate 2021
url https://doaj.org/article/c53e961158494961a6504a84794cf01b
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