A tunable and versatile chemogenetic near-infrared fluorescent reporter

被引:0
|
作者
El Hajji, Lina [1 ,2 ]
Bunel, Benjamin [3 ]
Joliot, Octave [4 ]
Li, Chenge [1 ]
Tebo, Alison G. [1 ,5 ]
Rampon, Christine [1 ,6 ]
Volovitch, Michel [1 ]
Fischer, Evelyne [3 ]
Pietrancosta, Nicolas [1 ,7 ]
Perez, Franck [4 ]
Morin, Xavier [3 ]
Vriz, Sophie [1 ,6 ]
Gautier, Arnaud [1 ,2 ,8 ]
机构
[1] Univ PSL, Sorbonne Univ, Ecole normale Super, CNRS,Chim Phys & Chim Vivant CPCV, F-75005 Paris, France
[2] Inst Curie, INSERM, CNRS, Chem Biol Canc CBC, F-75005 Paris, France
[3] Univ PSL, Ecole Normale Super, Inst Biol ENS IBENS, CNRS, F-75005 Paris, France
[4] Univ PSL, Inst Curie, CNRS, UMR144, Paris, France
[5] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA USA
[6] Univ Paris Cite, F-75006 Paris, France
[7] Sorbonne Univ, Neurosci Paris Seine Inst Biol Paris Seine NPS IBP, CNRS, INSERM, Paris, France
[8] Inst Univ France, Paris, France
基金
欧洲研究理事会;
关键词
PROTEIN;
D O I
10.1038/s41467-025-58017-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Near-infrared (NIR) fluorescent reporters open interesting perspectives for multiplexed imaging with higher contrast and depth using less toxic light. Here, we propose nirFAST, a small (14 kDa) chemogenetic NIR fluorescent reporter, displaying higher cellular brightness compared to top-performing NIR fluorescent proteins. nirFAST binds and stabilizes the fluorescent state of synthetic cell permeant fluorogenic chromophores (so-called fluorogens), otherwise dark when free. nirFAST displays tunable NIR, far-red or red emission through change of fluorogen. nirFAST allows imaging and spectral multiplexing in live cultured mammalian cells, chicken embryo tissues and zebrafish larvae. Its suitability for stimulated emission depletion nanoscopy enabled protein imaging with subdiffraction resolution in live cells. nirFAST enabled the design of a two-color cell cycle indicator for monitoring the different phases of the cell cycle. Finally, bisection of nirFAST allowed the design of a chemically induced dimerization technology with NIR fluorescence readout, enabling the control and visualization of protein proximity.
引用
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页数:17
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