High-fidelity optical reporting of neuronal electrical activity with an ultrafast fluorescent voltage sensor

被引:320
作者
St-Pierre, Francois [1 ,2 ]
Marshall, Jesse D. [3 ,4 ]
Yang, Ying [1 ,2 ]
Gong, Yiyang [3 ,4 ]
Schnitzer, Mark J. [3 ,4 ,5 ]
Lin, Michael Z. [1 ,2 ]
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
[3] Stanford Univ, James H Clark Ctr, Stanford, CA 94305 USA
[4] Stanford Univ, CNC Program, Palo Alto, CA 94304 USA
[5] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
MICROBIAL RHODOPSIN; ACTION-POTENTIALS; NEURAL ACTIVITY; PROTEIN; PROBE; MECHANISM; INTERNEURONS; INTEGRATION; INDICATORS; CIRCUITS;
D O I
10.1038/nn.3709
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Accurate optical reporting of electrical activity in genetically defined neuronal populations is a long-standing goal in neuroscience. We developed Accelerated Sensor of Action Potentials 1 (ASAP1), a voltage sensor design in which a circularly permuted green fluorescent protein is inserted in an extracellular loop of a voltage-sensing domain, rendering fluorescence responsive to membrane potential. ASAP1 demonstrated on and off kinetics of similar to 2 ms, reliably detected single action potentials and subthreshold potential changes, and tracked trains of action potential waveforms up to 200 Hz in single trials. With a favorable combination of brightness, dynamic range and speed, ASAP1 enables continuous monitoring of membrane potential in neurons at kilohertz frame rates using standard epifluorescence microscopy.
引用
收藏
页码:884 / 889
页数:6
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