Cyanine dye labeling reagents containing isothiocyanate groups

Abstract

New isothiocyanate derivatives of cyanine dyes were synthesized as fluorescent covalent labeling reagents for proteins and other biomolecules. These dyes have maximum absorbance in the red and near infrared regions of the spectrum, have high extinction coefficients and have adequate quantum yields. Incorporating two alkyl sulfonate groups in the dye stuctures increases their water solubility, which is beneficial for labeling biological molecules in aqueous solution. Reactivities of proteins with these new cyanines are similar to their reactivities with fluorescein isothiocyanate. These new labeling reagents are complementary to the fluorescein and rhodamine reagents, expanding the possibilities of multicolor analyses. Sheep anti‐mouse‐IgG antibody was labeled with a pentamethine cyanine dye (CY5.8‐ITC) and used with a fluoresceinated antibody as a second reagent for detecting human T‐cell subsets by flow cytometry. Copyright © 1989 Wiley‐Liss, Inc.