Publication | Open Access
Chemoselective ratiometric imaging of protein S-sulfenylation
15
Citations
22
References
2017
Year
Bioorganic ChemistryEngineeringMolecular BiologyChemoselective Ratiometric ImagingChemical ImageBioanalysisBioimagingMolecular ImagingBiochemistrySulfenic Acid ConjugationFluorous SynthesisRatiometric Fluorescent ProbeCurrent ProbesSingle-molecule DetectionBio-orthogonal ChemistryNatural SciencesCellular BiochemistryChemical ProbeSmall Molecules
Here we report a ratiometric fluorescent probe for chemoselective conjugation to sulfenic acids in living cells. Our approach couples an α-fluoro-substituted dimedone to an aminonaphthalene fluorophore (F-DiNap), which upon sulfenic acid conjugation is locked as the 1,3-diketone, changing the fluorophore excitation. F-DiNap reacts with S-sulfenylated proteins at equivalent rates to current probes, but the α-fluorine substitution blocks side-reactions with biological aldehydes.
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