A near-infrared genetically encoded calcium indicator for in vivo imaging

钙显像 体内 化学 细胞生物学 计算生物学 生物 遗传学 有机化学
作者
Anton A. Shemetov,Mikhail Monakhov,Qinrong Zhang,Jose Ernesto Canton-Josh,Manish Kumar,Maomao Chen,Mikhail E. Matlashov,Xuan Li,Wei Yang,Liming Nie,Daria M. Shcherbakova,Yevgenia Kozorovitskiy,Junjie Yao,Na Ji,Vladislav V. Verkhusha
出处
期刊:Nature Biotechnology [Nature Portfolio]
卷期号:39 (3): 368-377 被引量:109
标识
DOI:10.1038/s41587-020-0710-1
摘要

While calcium imaging has become a mainstay of modern neuroscience, the spectral properties of current fluorescent calcium indicators limit deep-tissue imaging as well as simultaneous use with other probes. Using two monomeric near-infrared (NIR) fluorescent proteins (FPs), we engineered an NIR Förster resonance energy transfer (FRET)-based genetically encoded calcium indicator (iGECI). iGECI exhibits high levels of brightness and photostability and an increase up to 600% in the fluorescence response to calcium. In dissociated neurons, iGECI detects spontaneous neuronal activity and electrically and optogenetically induced firing. We validated the performance of iGECI up to a depth of almost 400 µm in acute brain slices using one-photon light-sheet imaging. Applying hybrid photoacoustic and fluorescence microscopy, we simultaneously monitored neuronal and hemodynamic activities in the mouse brain through an intact skull, with resolutions of ~3 μm (lateral) and ~25–50 μm (axial). Using two-photon imaging, we detected evoked and spontaneous neuronal activity in the mouse visual cortex, with fluorescence changes of up to 25%. iGECI allows biosensors and optogenetic actuators to be multiplexed without spectral crosstalk. A near-infrared fluorescent calcium indicator can be combined with other optogenetic tools in vivo without spectral crosstalk.
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