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Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae

Channelrhodopsins guide algal phototaxis and are widely used as optogenetic probes for control of membrane potential with light. “Bacteriorhodopsin-like” cation channelrhodopsins (BCCRs) from cryptophytes differ in primary structure from other CCRs, lacking usual residues important for their cation...

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Autores principales: Sineshchekov, Oleg A., Govorunova, Elena G., Li, Hai, Wang, Yumei, Melkonian, Michael, Wong, Gane K.-S., Brown, Leonid S., Spudich, John L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175095/
https://www.ncbi.nlm.nih.gov/pubmed/32317325
http://dx.doi.org/10.1128/mBio.00657-20
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author Sineshchekov, Oleg A.
Govorunova, Elena G.
Li, Hai
Wang, Yumei
Melkonian, Michael
Wong, Gane K.-S.
Brown, Leonid S.
Spudich, John L.
author_facet Sineshchekov, Oleg A.
Govorunova, Elena G.
Li, Hai
Wang, Yumei
Melkonian, Michael
Wong, Gane K.-S.
Brown, Leonid S.
Spudich, John L.
author_sort Sineshchekov, Oleg A.
collection PubMed
description Channelrhodopsins guide algal phototaxis and are widely used as optogenetic probes for control of membrane potential with light. “Bacteriorhodopsin-like” cation channelrhodopsins (BCCRs) from cryptophytes differ in primary structure from other CCRs, lacking usual residues important for their cation conductance. Instead, the sequences of BCCR match more closely those of rhodopsin proton pumps, containing residues responsible for critical proton transfer reactions. We report 19 new BCCRs which, together with the earlier 6 known members of this family, form three branches (subfamilies) of a phylogenetic tree. Here, we show that the conductance mechanisms in two subfamilies differ with respect to involvement of the homolog of the proton donor in rhodopsin pumps. Two BCCRs from the genus Rhodomonas generate photocurrents that rapidly desensitize under continuous illumination. Using a combination of patch clamp electrophysiology, absorption, Raman spectroscopy, and flash photolysis, we found that the desensitization is due to rapid accumulation of a long-lived nonconducting intermediate of the photocycle with unusually blue-shifted absorption with a maximum at 330 nm. These observations reveal diversity within the BCCR family and contribute to deeper understanding of their independently evolved cation channel function.
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spelling pubmed-71750952020-04-27 Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae Sineshchekov, Oleg A. Govorunova, Elena G. Li, Hai Wang, Yumei Melkonian, Michael Wong, Gane K.-S. Brown, Leonid S. Spudich, John L. mBio Research Article Channelrhodopsins guide algal phototaxis and are widely used as optogenetic probes for control of membrane potential with light. “Bacteriorhodopsin-like” cation channelrhodopsins (BCCRs) from cryptophytes differ in primary structure from other CCRs, lacking usual residues important for their cation conductance. Instead, the sequences of BCCR match more closely those of rhodopsin proton pumps, containing residues responsible for critical proton transfer reactions. We report 19 new BCCRs which, together with the earlier 6 known members of this family, form three branches (subfamilies) of a phylogenetic tree. Here, we show that the conductance mechanisms in two subfamilies differ with respect to involvement of the homolog of the proton donor in rhodopsin pumps. Two BCCRs from the genus Rhodomonas generate photocurrents that rapidly desensitize under continuous illumination. Using a combination of patch clamp electrophysiology, absorption, Raman spectroscopy, and flash photolysis, we found that the desensitization is due to rapid accumulation of a long-lived nonconducting intermediate of the photocycle with unusually blue-shifted absorption with a maximum at 330 nm. These observations reveal diversity within the BCCR family and contribute to deeper understanding of their independently evolved cation channel function. American Society for Microbiology 2020-04-21 /pmc/articles/PMC7175095/ /pubmed/32317325 http://dx.doi.org/10.1128/mBio.00657-20 Text en Copyright © 2020 Sineshchekov et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Sineshchekov, Oleg A.
Govorunova, Elena G.
Li, Hai
Wang, Yumei
Melkonian, Michael
Wong, Gane K.-S.
Brown, Leonid S.
Spudich, John L.
Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae
title Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae
title_full Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae
title_fullStr Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae
title_full_unstemmed Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae
title_short Conductance Mechanisms of Rapidly Desensitizing Cation Channelrhodopsins from Cryptophyte Algae
title_sort conductance mechanisms of rapidly desensitizing cation channelrhodopsins from cryptophyte algae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175095/
https://www.ncbi.nlm.nih.gov/pubmed/32317325
http://dx.doi.org/10.1128/mBio.00657-20
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