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Bright and photostable chemigenetic indicators for extended in vivo voltage imaging
Author(s) -
Ahmed S. Abdelfattah,
Takashi Kawashima,
Amrita Singh,
Ondřej Novák,
Hui Liu,
Yichun Shuai,
Yi-Chieh Huang,
Luke Campagnola,
Stephanie C. Seeman,
Jianing Yu,
Jihong Zheng,
Jonathan B. Grimm,
Ronak Patel,
Johannes Friedrich,
Brett D. Mensh,
Liam Paninski,
J. J. Macklin,
Gabe J. Murphy,
Kaspar Podgorski,
BeiJung Lin,
TsaiWen Chen,
Glenn Turner,
Zhe Liu,
Minoru Koyama,
Karel Svoboda,
Misha B. Ahrens,
Luke D. Lavis,
Eric R. Schreiter
Publication year - 2019
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aav6416
Subject(s) - zebrafish , in vivo , fluorescent protein , subthreshold conduction , brightness , preclinical imaging , fluorescence , neuroscience , biology , biophysics , chemistry , voltage , green fluorescent protein , optics , biochemistry , physics , microbiology and biotechnology , gene , transistor , quantum mechanics
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.

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