| Literature DB >> 31835034 |
Vincent Villette1, Mariya Chavarha2, Ivan K Dimov3, Jonathan Bradley1, Lagnajeet Pradhan3, Benjamin Mathieu1, Stephen W Evans4, Simon Chamberland5, Dongqing Shi6, Renzhi Yang7, Benjamin B Kim8, Annick Ayon1, Abdelali Jalil9, François St-Pierre10, Mark J Schnitzer11, Guoqiang Bi12, Katalin Toth5, Jun Ding13, Stéphane Dieudonné14, Michael Z Lin15.
Abstract
Optical interrogation of voltage in deep brain locations with cellular resolution would be immensely useful for understanding how neuronal circuits process information. Here, we report ASAP3, a genetically encoded voltage indicator with 51% fluorescence modulation by physiological voltages, submillisecond activation kinetics, and full responsivity under two-photon excitation. We also introduce an ultrafast local volume excitation (ULoVE) method for kilohertz-rate two-photon sampling in vivo with increased stability and sensitivity. Combining a soma-targeted ASAP3 variant and ULoVE, we show single-trial tracking of spikes and subthreshold events for minutes in deep locations, with subcellular resolution and with repeated sampling over days. In the visual cortex, we use soma-targeted ASAP3 to illustrate cell-type-dependent subthreshold modulation by locomotion. Thus, ASAP3 and ULoVE enable high-speed optical recording of electrical activity in genetically defined neurons at deep locations during awake behavior.Entities:
Keywords: ASAP3; GEVI; RAMP; ULoVE; action potential; electrophysiology; electroporation; theta oscillation; two-photon; voltage imaging
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Year: 2019 PMID: 31835034 PMCID: PMC6941988 DOI: 10.1016/j.cell.2019.11.004
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582