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A calibrated optogenetic toolbox of stable zebrafish opsin lines
Optogenetic actuators with diverse spectral tuning, ion selectivity and kinetics are constantly being engineered providing powerful tools for controlling neural activity with subcellular resolution and millisecond precision. Achieving reliable and interpretable in vivo optogenetic manipulations requ...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170653/ https://www.ncbi.nlm.nih.gov/pubmed/32216873 http://dx.doi.org/10.7554/eLife.54937 |
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author | Antinucci, Paride Dumitrescu, Adna Deleuze, Charlotte Morley, Holly J Leung, Kristie Hagley, Tom Kubo, Fumi Baier, Herwig Bianco, Isaac H Wyart, Claire |
author_facet | Antinucci, Paride Dumitrescu, Adna Deleuze, Charlotte Morley, Holly J Leung, Kristie Hagley, Tom Kubo, Fumi Baier, Herwig Bianco, Isaac H Wyart, Claire |
author_sort | Antinucci, Paride |
collection | PubMed |
description | Optogenetic actuators with diverse spectral tuning, ion selectivity and kinetics are constantly being engineered providing powerful tools for controlling neural activity with subcellular resolution and millisecond precision. Achieving reliable and interpretable in vivo optogenetic manipulations requires reproducible actuator expression and calibration of photocurrents in target neurons. Here, we developed nine transgenic zebrafish lines for stable opsin expression and calibrated their efficacy in vivo. We first used high-throughput behavioural assays to compare opsin ability to elicit or silence neural activity. Next, we performed in vivo whole-cell electrophysiological recordings to quantify the amplitude and kinetics of photocurrents and test opsin ability to precisely control spiking. We observed substantial variation in efficacy, associated with differences in both opsin expression level and photocurrent characteristics, and identified conditions for optimal use of the most efficient opsins. Overall, our calibrated optogenetic toolkit will facilitate the design of controlled optogenetic circuit manipulations. |
format | Online Article Text |
id | pubmed-7170653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71706532020-04-22 A calibrated optogenetic toolbox of stable zebrafish opsin lines Antinucci, Paride Dumitrescu, Adna Deleuze, Charlotte Morley, Holly J Leung, Kristie Hagley, Tom Kubo, Fumi Baier, Herwig Bianco, Isaac H Wyart, Claire eLife Neuroscience Optogenetic actuators with diverse spectral tuning, ion selectivity and kinetics are constantly being engineered providing powerful tools for controlling neural activity with subcellular resolution and millisecond precision. Achieving reliable and interpretable in vivo optogenetic manipulations requires reproducible actuator expression and calibration of photocurrents in target neurons. Here, we developed nine transgenic zebrafish lines for stable opsin expression and calibrated their efficacy in vivo. We first used high-throughput behavioural assays to compare opsin ability to elicit or silence neural activity. Next, we performed in vivo whole-cell electrophysiological recordings to quantify the amplitude and kinetics of photocurrents and test opsin ability to precisely control spiking. We observed substantial variation in efficacy, associated with differences in both opsin expression level and photocurrent characteristics, and identified conditions for optimal use of the most efficient opsins. Overall, our calibrated optogenetic toolkit will facilitate the design of controlled optogenetic circuit manipulations. eLife Sciences Publications, Ltd 2020-03-27 /pmc/articles/PMC7170653/ /pubmed/32216873 http://dx.doi.org/10.7554/eLife.54937 Text en © 2020, Antinucci et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Antinucci, Paride Dumitrescu, Adna Deleuze, Charlotte Morley, Holly J Leung, Kristie Hagley, Tom Kubo, Fumi Baier, Herwig Bianco, Isaac H Wyart, Claire A calibrated optogenetic toolbox of stable zebrafish opsin lines |
title | A calibrated optogenetic toolbox of stable zebrafish opsin lines |
title_full | A calibrated optogenetic toolbox of stable zebrafish opsin lines |
title_fullStr | A calibrated optogenetic toolbox of stable zebrafish opsin lines |
title_full_unstemmed | A calibrated optogenetic toolbox of stable zebrafish opsin lines |
title_short | A calibrated optogenetic toolbox of stable zebrafish opsin lines |
title_sort | calibrated optogenetic toolbox of stable zebrafish opsin lines |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170653/ https://www.ncbi.nlm.nih.gov/pubmed/32216873 http://dx.doi.org/10.7554/eLife.54937 |
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