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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6882325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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