| Literature DB >> 31371562 |
Ahmed S Abdelfattah1, Takashi Kawashima1, Amrita Singh1,2, Ondrej Novak1,3, Hui Liu1, Yichun Shuai1, Yi-Chieh Huang4, Luke Campagnola5, Stephanie C Seeman5, Jianing Yu1, Jihong Zheng1, Jonathan B Grimm1, Ronak Patel1, Johannes Friedrich6,7,8, Brett D Mensh1, Liam Paninski6,7, John J Macklin1, Gabe J Murphy5, Kaspar Podgorski1, Bei-Jung Lin4, Tsai-Wen Chen4, Glenn C Turner1, Zhe Liu1, Minoru Koyama1, Karel Svoboda1, Misha B Ahrens1, Luke D Lavis1, Eric R Schreiter9.
Abstract
Genetically encoded voltage indicators (GEVIs) enable monitoring of neuronal activity at high spatial and temporal resolution. However, the utility of existing GEVIs has been limited by the brightness and photostability of fluorescent proteins and rhodopsins. We engineered a GEVI, called Voltron, that uses bright and photostable synthetic dyes instead of protein-based fluorophores, thereby extending the number of neurons imaged simultaneously in vivo by a factor of 10 and enabling imaging for significantly longer durations relative to existing GEVIs. We used Voltron for in vivo voltage imaging in mice, zebrafish, and fruit flies. In the mouse cortex, Voltron allowed single-trial recording of spikes and subthreshold voltage signals from dozens of neurons simultaneously over a 15-minute period of continuous imaging. In larval zebrafish, Voltron enabled the precise correlation of spike timing with behavior.Entities:
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Year: 2019 PMID: 31371562 DOI: 10.1126/science.aav6416
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728