A tunable and versatile chemogenetic near-infrared fluorescent reporter

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.

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Publication Details

Journal
Nature Communications
Published
2025-03-16
DOI
https://doi.org/10.1038/s41467-025-58017-9
Citations
7
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
4.72
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article

A tunable and versatile chemogenetic near-infrared fluorescent reporter

Octave Joliot, Evelyne Fischer, Lina El Hajji, Franck Perez et al.
7 citations
Nature Communications
Nanoplatforms for cancer theranostics
4.72
article

A tunable and versatile chemogenetic near-infrared fluorescent reporter

Octave Joliot, Evelyne Fischer, Lina El Hajji, Franck Perez, Xavier Morin, Christine Rampon, Chenge Li, Sophie Vriz, Arnaud Gautier, Alison G. Tebo, Michel Volovitch, Nicolas Pietrancosta, Benjamin Bunel
article en
7 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Institut Universitaire de France (FR), Janelia Research Campus (US), Université Paris Cité (FR), Université Paris Sciences et Lettres (FR), École Normale Supérieure - PSL (FR), Sorbonne Université (FR), École Normale Supérieure (BI), Institut de Biologie Paris-Seine (FR), Institut de Biologie de l'École Normale Supérieure (FR), Biologie cellulaire et Cancer (FR), Neurosciences Paris-Seine (FR), Institut Curie (FR)
Openalex Percentile: Top 5%
Nanoplatforms for cancer theranostics
4.72
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