Nature MethodsSynthetic BiologyPeer-reviewed journal article
Engineering of NEMO as calcium indicators with large dynamics and high sensitivity
JIA LIN LIiD, Ziwei ShangiD, Jiahui CheniD, Wenjia Gu, Li YaoiD, Xin YangiD, Xiaowen Sun, Liuqing WangiD, Tianlu WangiD, Siyao LiuiD, Jiajing LiiD, Tingting Hou, Dajun XingiD, Donald L. GilliD, Jiejie LiiD, Shi‐Qiang WangiD, Lijuan HouiD, Yubin ZhouiD, Ai‐Hui TangiD, Xiaohui ZhangiD, Youjun WangiD
Abstract
Genetically-encoded calcium indicators (GECI) are indispensable tools for real-time monitoring of intracellular calcium signals and cellular activities in living organisms. Current GECIs face the challenge of sub-optimal peak signal-to-baseline-ratio (SBR) with limited resolution for reporting subtle calcium transients. We report herein the development of a suite of calcium sensors, designated NEMO, with fast kinetics and wide dynamic ranges (>100-fold). NEMO indicators report Ca2+ transients with peak SBRs ~20-fold larger than the top-of-the-range GCaMP series. NEMO sensors further enable the quantification of absolution calcium concentration with ratiometric or photochromic imaging. Compared to GCaMPs, NEMOs could detect single action potentials in neurons with a peak SBR two times higher and a median peak SBR four times larger in vivo, thereby outperforming most existing state-of-the-art GECIs. Given their high sensitivity and resolution to report intracellular Ca2+ signals, NEMO sensors may find broad applications in monitoring neuronal activities and other Ca2+-modulated physiological processes in both mammals and plants.
- organism: mouse
- organism: plant (other)
- assay: imaging
- research focus: protein design
- approach: experimental assay
- Citations
- 58
- FWCI
- 7.01
- Field percentile
- top 2%
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