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The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin

The new class of microbial rhodopsins, called xenorhodopsins (XeRs),([1]) extends the versatility of this family by inward H(+) pumps.([2–4]) These pumps are an alternative optogenetic tool to the light‐gated ion channels (e.g. ChR1,2), because the activation of electrically excitable cells by XeRs...

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Autores principales: Weissbecker, Juliane, Boumrifak, Chokri, Breyer, Maximilian, Wießalla, Tristan, Shevchenko, Vitaly, Mager, Thomas, Slavov, Chavdar, Alekseev, Alexey, Kovalev, Kirill, Gordeliy, Valentin, Bamberg, Ernst, Wachtveitl, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518763/
https://www.ncbi.nlm.nih.gov/pubmed/34339559
http://dx.doi.org/10.1002/anie.202103882
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author Weissbecker, Juliane
Boumrifak, Chokri
Breyer, Maximilian
Wießalla, Tristan
Shevchenko, Vitaly
Mager, Thomas
Slavov, Chavdar
Alekseev, Alexey
Kovalev, Kirill
Gordeliy, Valentin
Bamberg, Ernst
Wachtveitl, Josef
author_facet Weissbecker, Juliane
Boumrifak, Chokri
Breyer, Maximilian
Wießalla, Tristan
Shevchenko, Vitaly
Mager, Thomas
Slavov, Chavdar
Alekseev, Alexey
Kovalev, Kirill
Gordeliy, Valentin
Bamberg, Ernst
Wachtveitl, Josef
author_sort Weissbecker, Juliane
collection PubMed
description The new class of microbial rhodopsins, called xenorhodopsins (XeRs),([1]) extends the versatility of this family by inward H(+) pumps.([2–4]) These pumps are an alternative optogenetic tool to the light‐gated ion channels (e.g. ChR1,2), because the activation of electrically excitable cells by XeRs is independent from the surrounding physiological conditions. In this work we functionally and spectroscopically characterized XeR from Nanosalina (NsXeR).([1]) The photodynamic behavior of NsXeR was investigated on the ps to s time scale elucidating the formation of the J and K and a previously unknown long‐lived intermediate. The pH dependent kinetics reveal that alkalization of the surrounding medium accelerates the photocycle and the pump turnover. In patch‐clamp experiments the blue‐light illumination of NsXeR in the M state shows a potential‐dependent vectoriality of the photocurrent transients, suggesting a variable accessibility of reprotonation of the retinal Schiff base. Insights on the kinetically independent switching mechanism could furthermore be obtained by mutational studies on the putative intracellular H(+) acceptor D220.
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spelling pubmed-85187632021-10-21 The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin Weissbecker, Juliane Boumrifak, Chokri Breyer, Maximilian Wießalla, Tristan Shevchenko, Vitaly Mager, Thomas Slavov, Chavdar Alekseev, Alexey Kovalev, Kirill Gordeliy, Valentin Bamberg, Ernst Wachtveitl, Josef Angew Chem Int Ed Engl Research Articles The new class of microbial rhodopsins, called xenorhodopsins (XeRs),([1]) extends the versatility of this family by inward H(+) pumps.([2–4]) These pumps are an alternative optogenetic tool to the light‐gated ion channels (e.g. ChR1,2), because the activation of electrically excitable cells by XeRs is independent from the surrounding physiological conditions. In this work we functionally and spectroscopically characterized XeR from Nanosalina (NsXeR).([1]) The photodynamic behavior of NsXeR was investigated on the ps to s time scale elucidating the formation of the J and K and a previously unknown long‐lived intermediate. The pH dependent kinetics reveal that alkalization of the surrounding medium accelerates the photocycle and the pump turnover. In patch‐clamp experiments the blue‐light illumination of NsXeR in the M state shows a potential‐dependent vectoriality of the photocurrent transients, suggesting a variable accessibility of reprotonation of the retinal Schiff base. Insights on the kinetically independent switching mechanism could furthermore be obtained by mutational studies on the putative intracellular H(+) acceptor D220. John Wiley and Sons Inc. 2021-09-15 2021-10-11 /pmc/articles/PMC8518763/ /pubmed/34339559 http://dx.doi.org/10.1002/anie.202103882 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Weissbecker, Juliane
Boumrifak, Chokri
Breyer, Maximilian
Wießalla, Tristan
Shevchenko, Vitaly
Mager, Thomas
Slavov, Chavdar
Alekseev, Alexey
Kovalev, Kirill
Gordeliy, Valentin
Bamberg, Ernst
Wachtveitl, Josef
The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin
title The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin
title_full The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin
title_fullStr The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin
title_full_unstemmed The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin
title_short The Voltage Dependent Sidedness of the Reprotonation of the Retinal Schiff Base Determines the Unique Inward Pumping of Xenorhodopsin
title_sort voltage dependent sidedness of the reprotonation of the retinal schiff base determines the unique inward pumping of xenorhodopsin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518763/
https://www.ncbi.nlm.nih.gov/pubmed/34339559
http://dx.doi.org/10.1002/anie.202103882
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