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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2017-08-01
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Online Access: | https://doi.org/10.1038/s41598-017-08731-2 |
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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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