A genetically encoded Ca2+ indicator based on circularly permutated sea anemone red fluorescent protein eqFP578

BMC Biology - Tập 16 - Trang 1-16 - 2018
Yi Shen1, Hod Dana2,3, Ahmed S. Abdelfattah1,4, Ronak Patel2, Jamien Shea2, Rosana S. Molina5, Bijal Rawal6, Vladimir Rancic6, Yu-Fen Chang7, Lanshi Wu1, Yingche Chen1, Yong Qian1, Matthew D. Wiens1, Nathan Hambleton1, Klaus Ballanyi6, Thomas E. Hughes5, Mikhail Drobizhev5, Douglas S. Kim2, Minoru Koyama2, Eric R. Schreiter2, Robert E. Campbell1
1Department of Chemistry, University of Alberta, Edmonton, Canada
2Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, USA
3Present address: Department of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, USA
4Present address: Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, USA
5Department of Cell Biology and Neuroscience, Montana State University, Bozeman, USA
6Department of Physiology, University of Alberta, Edmonton, Canada
7LumiSTAR Biotechnology Incorporation, Taipei City, Taiwan

Tóm tắt

Genetically encoded calcium ion (Ca2+) indicators (GECIs) are indispensable tools for measuring Ca2+ dynamics and neuronal activities in vitro and in vivo. Red fluorescent protein (RFP)-based GECIs have inherent advantages relative to green fluorescent protein-based GECIs due to the longer wavelength light used for excitation. Longer wavelength light is associated with decreased phototoxicity and deeper penetration through tissue. Red GECI can also enable multicolor visualization with blue- or cyan-excitable fluorophores. Here we report the development, structure, and validation of a new RFP-based GECI, K-GECO1, based on a circularly permutated RFP derived from the sea anemone Entacmaea quadricolor. We have characterized the performance of K-GECO1 in cultured HeLa cells, dissociated neurons, stem-cell-derived cardiomyocytes, organotypic brain slices, zebrafish spinal cord in vivo, and mouse brain in vivo. K-GECO1 is the archetype of a new lineage of GECIs based on the RFP eqFP578 scaffold. It offers high sensitivity and fast kinetics, similar or better than those of current state-of-the-art indicators, with diminished lysosomal accumulation and minimal blue-light photoactivation. Further refinements of the K-GECO1 lineage could lead to further improved variants with overall performance that exceeds that of the most highly optimized red GECIs.

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