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Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition

BACKGROUND: Optogenetic silencing techniques have expanded the causal understanding of the functions of diverse neuronal cell types in both the healthy and diseased brain. A widely used inhibitory optogenetic actuator is eNpHR3.0, an improved version of the light-driven chloride pump halorhodopsin d...

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Autores principales: Zhang, Chuanqiang, Yang, Shang, Flossmann, Tom, Gao, Shiqiang, Witte, Otto W., Nagel, Georg, Holthoff, Knut, Kirmse, Knut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882325/
https://www.ncbi.nlm.nih.gov/pubmed/31775747
http://dx.doi.org/10.1186/s12915-019-0717-6
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author Zhang, Chuanqiang
Yang, Shang
Flossmann, Tom
Gao, Shiqiang
Witte, Otto W.
Nagel, Georg
Holthoff, Knut
Kirmse, Knut
author_facet Zhang, Chuanqiang
Yang, Shang
Flossmann, Tom
Gao, Shiqiang
Witte, Otto W.
Nagel, Georg
Holthoff, Knut
Kirmse, Knut
author_sort Zhang, Chuanqiang
collection PubMed
description BACKGROUND: Optogenetic silencing techniques have expanded the causal understanding of the functions of diverse neuronal cell types in both the healthy and diseased brain. A widely used inhibitory optogenetic actuator is eNpHR3.0, an improved version of the light-driven chloride pump halorhodopsin derived from Natronomonas pharaonis. A major drawback of eNpHR3.0 is related to its pronounced inactivation on a time-scale of seconds, which renders it unsuited for applications that require long-lasting silencing. RESULTS: Using transgenic mice and Xenopus laevis oocytes expressing an eNpHR3.0-EYFP fusion protein, we here report optimized photo-stimulation techniques that profoundly increase the stability of eNpHR3.0-mediated currents during long-term photo-stimulation. We demonstrate that optimized photo-stimulation enables prolonged hyperpolarization and suppression of action potential discharge on a time-scale of minutes. CONCLUSIONS: Collectively, our findings extend the utility of eNpHR3.0 to the long-lasting inhibition of excitable cells, thus facilitating the optogenetic dissection of neural circuits.
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spelling pubmed-68823252019-12-03 Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition Zhang, Chuanqiang Yang, Shang Flossmann, Tom Gao, Shiqiang Witte, Otto W. Nagel, Georg Holthoff, Knut Kirmse, Knut BMC Biol Methodology Article BACKGROUND: Optogenetic silencing techniques have expanded the causal understanding of the functions of diverse neuronal cell types in both the healthy and diseased brain. A widely used inhibitory optogenetic actuator is eNpHR3.0, an improved version of the light-driven chloride pump halorhodopsin derived from Natronomonas pharaonis. A major drawback of eNpHR3.0 is related to its pronounced inactivation on a time-scale of seconds, which renders it unsuited for applications that require long-lasting silencing. RESULTS: Using transgenic mice and Xenopus laevis oocytes expressing an eNpHR3.0-EYFP fusion protein, we here report optimized photo-stimulation techniques that profoundly increase the stability of eNpHR3.0-mediated currents during long-term photo-stimulation. We demonstrate that optimized photo-stimulation enables prolonged hyperpolarization and suppression of action potential discharge on a time-scale of minutes. CONCLUSIONS: Collectively, our findings extend the utility of eNpHR3.0 to the long-lasting inhibition of excitable cells, thus facilitating the optogenetic dissection of neural circuits. BioMed Central 2019-11-27 /pmc/articles/PMC6882325/ /pubmed/31775747 http://dx.doi.org/10.1186/s12915-019-0717-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Zhang, Chuanqiang
Yang, Shang
Flossmann, Tom
Gao, Shiqiang
Witte, Otto W.
Nagel, Georg
Holthoff, Knut
Kirmse, Knut
Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
title Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
title_full Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
title_fullStr Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
title_full_unstemmed Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
title_short Optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
title_sort optimized photo-stimulation of halorhodopsin for long-term neuronal inhibition
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882325/
https://www.ncbi.nlm.nih.gov/pubmed/31775747
http://dx.doi.org/10.1186/s12915-019-0717-6
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