High-speed recording of neural spikes in awake mice and flies with a fluorescent voltage sensor

被引:333
作者
Gong, Yiyang [1 ,2 ,3 ]
Huang, Cheng [1 ]
Li, Jin Zhong [1 ,2 ]
Grewe, Benjamin F. [1 ,2 ]
Zhang, Yanping [1 ,2 ,4 ]
Eismann, Stephan [1 ,2 ]
Schnitzer, Mark J. [1 ,2 ,4 ]
机构
[1] Stanford Univ, James H Clark Ctr, Stanford, CA 94305 USA
[2] Stanford Univ, CNC Program, Stanford, CA 94305 USA
[3] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
关键词
DROSOPHILA ANTENNAL LOBE; MOUSE VISUAL-CORTEX; NEURONAL-ACTIVITY; FRET; CIRCUITS; PROTEINS; BURSTS; BRIGHT;
D O I
10.1126/science.aab0810
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genetically encoded voltage indicators (GEVIs) are a promising technology for fluorescence readout of millisecond-scale neuronal dynamics. Previous GEVIs had insufficient signaling speed and dynamic range to resolve action potentials in live animals. We coupled fast voltage-sensing domains from a rhodopsin protein to bright fluorophores through resonance energy transfer. The resulting GEVIs are sufficiently bright and fast to report neuronal action potentials and membrane voltage dynamics in awake mice and flies, resolving fast spike trains with 0.2-millisecond timing precision at spike detection error rates orders of magnitude better than previous GEVIs. In vivo imaging revealed sensory-evoked responses, including somatic spiking, dendritic dynamics, and intracellular voltage propagation. These results empower in vivo optical studies of neuronal electrophysiology and coding and motivate further advancements in high-speed microscopy.
引用
收藏
页码:1361 / 1366
页数:6
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