Abstract
A simple one-pot-procedure for preparation of protein-reactive, water-soluble merocyanine and cyanine dyes has been developed. The 1-(3-ammoniopropyl)-2,3,3-trimethyl-3H-indolium-5-sulfonate bromide (1) was used as a common starting intermediate. The method allows easy preparation of dyes with chloro- and iodoacetamide side chains for covalent attachment to cysteine. By placing a sulfonato group directly on the dye fluorophore system, dyes with high fluorescence quantum yields in water were generated. Both iodo- and chloroacetamido derivatives were shown to be useful in protein labeling. Less reactive chloroacetamides will be preferential for selective labeling of the most reactive cysteines.
MeSH Terms
Carbocyanines/chemistry,metabolism
Cysteine/chemistry
Diagnostic Imaging
Fluorescent Dyes/chemical synthesis,chemistry,metabolism
Green Fluorescent Proteins/metabolism
Mitogen-Activated Protein Kinase 1/metabolism
Pyrimidinones/chemistry,metabolism
Recombinant Fusion Proteins/metabolism
Solubility
Water
Chemicals
Carbocyanines
Fluorescent Dyes
Pyrimidinones
Recombinant Fusion Proteins
enhanced green fluorescent protein
Water
Green Fluorescent Proteins
merocyanine dye
Mitogen-Activated Protein Kinase 1
Cysteine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Toutchkine Alexei
Department of Pharmacology and Lineberger Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA. alexei.toutchkine@sial.com
Nguyen Dan-Vinh
Hahn Klaus M
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