Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition

Abstract An improved genetically encoded voltage indicator (GEVI) was achieved by altering the charge composition of the region linking the voltage-sensing domain of the GEVI to a pH-sensitive fluorescent protein. Negatively charged linker segments reduced the voltage-dependent optical signal while...

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Main Authors: Sungmoo Lee, Tristan Geiller, Arong Jung, Ryuichi Nakajima, Yoon-Kyu Song, Bradley J. Baker
Format: Article
Language:English
Published: Nature Publishing Group 2017-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-08731-2
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spelling doaj-fccba8cd2d084bddb5510817b58c16d42020-12-08T02:33:33ZengNature Publishing GroupScientific Reports2045-23222017-08-017111610.1038/s41598-017-08731-2Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge compositionSungmoo Lee0Tristan Geiller1Arong Jung2Ryuichi Nakajima3Yoon-Kyu Song4Bradley J. Baker5The Center for Functional Connectomics, Korea Institute of Science and TechnologyThe Center for Functional Connectomics, Korea Institute of Science and TechnologyThe Center for Functional Connectomics, Korea Institute of Science and TechnologyThe Center for Functional Connectomics, Korea Institute of Science and TechnologyDepartment of Transdisciplinary Studies, Graduate School of Convergence Science and Technology, Seoul National UniversityThe Center for Functional Connectomics, Korea Institute of Science and TechnologyAbstract An improved genetically encoded voltage indicator (GEVI) was achieved by altering the charge composition of the region linking the voltage-sensing domain of the GEVI to a pH-sensitive fluorescent protein. Negatively charged linker segments reduced the voltage-dependent optical signal while positively charged linkers increased the signal size. Arginine scanning mutagenesis of the linker region improved the signal size of the GEVI, Bongwoori, yielding fluorescent signals as high as 20% ΔF/F during the firing of action potentials. The speed of this new sensor was also capable of optically resolving action potentials firing at 65 Hz. This large signal size enabled individual pixels to become surrogate electrodes. Plotting the highest correlated pixels based only on fluorescence changes reproduced the image of the neuron exhibiting activity. Furthermore, the use of a pH-sensitive fluorescent protein facilitated the detection of the acidification of the neuron during the firing of action potentials.https://doi.org/10.1038/s41598-017-08731-2
collection DOAJ
language English
format Article
sources DOAJ
author Sungmoo Lee
Tristan Geiller
Arong Jung
Ryuichi Nakajima
Yoon-Kyu Song
Bradley J. Baker
spellingShingle Sungmoo Lee
Tristan Geiller
Arong Jung
Ryuichi Nakajima
Yoon-Kyu Song
Bradley J. Baker
Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
Scientific Reports
author_facet Sungmoo Lee
Tristan Geiller
Arong Jung
Ryuichi Nakajima
Yoon-Kyu Song
Bradley J. Baker
author_sort Sungmoo Lee
title Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
title_short Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
title_full Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
title_fullStr Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
title_full_unstemmed Improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
title_sort improving a genetically encoded voltage indicator by modifying the cytoplasmic charge composition
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-08-01
description Abstract An improved genetically encoded voltage indicator (GEVI) was achieved by altering the charge composition of the region linking the voltage-sensing domain of the GEVI to a pH-sensitive fluorescent protein. Negatively charged linker segments reduced the voltage-dependent optical signal while positively charged linkers increased the signal size. Arginine scanning mutagenesis of the linker region improved the signal size of the GEVI, Bongwoori, yielding fluorescent signals as high as 20% ΔF/F during the firing of action potentials. The speed of this new sensor was also capable of optically resolving action potentials firing at 65 Hz. This large signal size enabled individual pixels to become surrogate electrodes. Plotting the highest correlated pixels based only on fluorescence changes reproduced the image of the neuron exhibiting activity. Furthermore, the use of a pH-sensitive fluorescent protein facilitated the detection of the acidification of the neuron during the firing of action potentials.
url https://doi.org/10.1038/s41598-017-08731-2
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