Author:
Abdelfattah Ahmed S.,Kawashima Takashi,Singh Amrita,Novak Ondrej,Liu Hui,Shuai Yichun,Huang Yi-Chieh,Grimm Jonathan B.,Patel Ronak,Friedrich Johannes,Mensh Brett D.,Paninski Liam,Macklin John J.,Podgorski Kaspar,Lin Bei-Jung,Chen Tsai-Wen,Turner Glenn C.,Liu Zhe,Koyama Minoru,Svoboda Karel,Ahrens Misha B.,Lavis Luke D.,Schreiter Eric R.
Abstract
AbstractImaging changes in membrane potential using genetically encoded fluorescent voltage indicators (GEVIs) has great potential for monitoring neuronal activity with high spatial and temporal resolution. Brightness and photostability of fluorescent proteins and rhodopsins have limited the utility of existing GEVIs. We engineered a novel GEVI, ‘Voltron’, that utilizes bright and photostable synthetic dyes instead of protein-based fluorophores, extending the combined duration of imaging and number of neurons imaged simultaneously by more than tenfold relative to existing GEVIs. We used Voltron for in vivo voltage imaging in mice, zebrafish, and fruit flies. In mouse cortex, Voltron allowed single-trial recording of spikes and subthreshold voltage signals from dozens of neurons simultaneously, over 15 minutes of continuous imaging. In larval zebrafish, Voltron enabled the precise correlation of spike timing with behavior.
Publisher
Cold Spring Harbor Laboratory
Cited by
14 articles.
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