| Literature DB >> 25314130 |
Yingche Chen1, Christopher M Clouthier, Kelvin Tsao, Miroslava Strmiskova, Hugo Lachance, Jeffrey W Keillor.
Abstract
A fluorescent protein-labeling strategy was developed in which a protein of interest (POI) is genetically tagged with a short peptide sequence presenting two Cys residues that can selectively react with synthetic fluorogenic reagents. These fluorogens comprise a fluorophore and two maleimide groups that quench fluorescence until they both undergo thiol addition during the labeling reaction. Novel fluorogens were prepared and kinetically characterized to demonstrate the importance of a methoxy substituent on the maleimide in suppressing reactivity with glutathione, an intracellular thiol, while maintaining reactivity with the dithiol tag. This system allows the rapid and specific labeling of intracellular POIs.Entities:
Keywords: bioorthogonal chemistry; fluorescent probes; glutathione; maleimide; protein labeling
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Year: 2014 PMID: 25314130 DOI: 10.1002/anie.201408015
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336