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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8518763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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