钙显像
神经油
神经突
运动前神经元活动
钙
生物物理学
荧光寿命成像显微镜
神经元
化学
生物
神经科学
荧光
中枢神经系统
生物化学
体外
物理
有机化学
量子力学
作者
Hod Dana,Yi Sun,Boaz Mohar,Brad K. Hulse,Aaron Kerlin,J. Hasseman,Getahun Tsegaye,Arthur Tsang,Allan M. Wong,Ronak Patel,John J. Macklin,Chen Yang,Arthur Konnerth,Vivek Jayaraman,Loren L. Looger,Eric R. Schreiter,Karel Svoboda,Douglas S. Kim
出处
期刊:Nature Methods
[Springer Nature]
日期:2019-06-17
卷期号:16 (7): 649-657
被引量:993
标识
DOI:10.1038/s41592-019-0435-6
摘要
Calcium imaging with genetically encoded calcium indicators (GECIs) is routinely used to measure neural activity in intact nervous systems. GECIs are frequently used in one of two different modes: to track activity in large populations of neuronal cell bodies, or to follow dynamics in subcellular compartments such as axons, dendrites and individual synaptic compartments. Despite major advances, calcium imaging is still limited by the biophysical properties of existing GECIs, including affinity, signal-to-noise ratio, rise and decay kinetics and dynamic range. Using structure-guided mutagenesis and neuron-based screening, we optimized the green fluorescent protein-based GECI GCaMP6 for different modes of in vivo imaging. The resulting jGCaMP7 sensors provide improved detection of individual spikes (jGCaMP7s,f), imaging in neurites and neuropil (jGCaMP7b), and may allow tracking larger populations of neurons using two-photon (jGCaMP7s,f) or wide-field (jGCaMP7c) imaging.
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