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fmolb.2021.738829.pdf | 1.19 MB | Adobe PDF | 見る/開く |
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DCフィールド | 値 | 言語 |
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dc.contributor.author | Zhang, Xiao Min | en |
dc.contributor.author | Yokoyama, Tatsushi | en |
dc.contributor.author | Sakamoto, Masayuki | en |
dc.contributor.alternative | 横山, 達士 | ja |
dc.contributor.alternative | 坂本, 雅行 | ja |
dc.date.accessioned | 2022-03-03T09:22:10Z | - |
dc.date.available | 2022-03-03T09:22:10Z | - |
dc.date.issued | 2021 | - |
dc.identifier.uri | http://hdl.handle.net/2433/268287 | - |
dc.description.abstract | Membrane potential is the critical parameter that reflects the excitability of a neuron, and it is usually measured by electrophysiological recordings with electrodes. However, this is an invasive approach that is constrained by the problems of lacking spatial resolution and genetic specificity. Recently, the development of a variety of fluorescent probes has made it possible to measure the activity of individual cells with high spatiotemporal resolution. The adaptation of this technique to image electrical activity in neurons has become an informative method to study neural circuits. Genetically encoded voltage indicators (GEVIs) can be used with superior performance to accurately target specific genetic populations and reveal neuronal dynamics on a millisecond scale. Microbial rhodopsins are commonly used as optogenetic actuators to manipulate neuronal activities and to explore the circuit mechanisms of brain function, but they also can be used as fluorescent voltage indicators. In this review, we summarize recent advances in the design and the application of rhodopsin-based GEVIs. | en |
dc.language.iso | eng | - |
dc.publisher | Frontiers Media SA | en |
dc.rights | © 2021 Zhang, Yokoyama and Sakamoto. | en |
dc.rights | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | voltage imaging | en |
dc.subject | microbial rhodopsins | en |
dc.subject | photocycle | en |
dc.subject | FRET (förster resonance energy transfer) | en |
dc.subject | optogenetics | en |
dc.subject | in vivo imaging | en |
dc.title | Imaging Voltage with Microbial Rhodopsins | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Frontiers in Molecular Biosciences | en |
dc.identifier.volume | 8 | - |
dc.relation.doi | 10.3389/fmolb.2021.738829 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 738829 | - |
dc.identifier.pmid | 34513932 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 20H04122 | - |
datacite.awardNumber | 21K19429 | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20H04122/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-21K19429/ | - |
dc.identifier.eissn | 2296-889X | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.awardTitle | 多光子4Dイメージングによる生後発達期における新生ニューロンの機能的意義の解明 | ja |
jpcoar.awardTitle | 多光子励起による生体多色活動計測・操作技術の開発と応用 | ja |
出現コレクション: | 学術雑誌掲載論文等 |

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