J. Baranowskakortylewicz et Ai. Kassis, LABELING OF IMMUNOGLOBULINS WITH BIFUNCTIONAL, SULFHYDRYL-SELECTIVE, AND PHOTOREACTIVE COUMARINS, Bioconjugate chemistry, 4(4), 1993, pp. 300-304
4-(Bromomethyl)-6,7-dimethoxy-2-oxo-2H-benzopyran (1a) and 4-(bromomet
hyl)-7-methoxy-2-oxo-2H-benzopyran (1b) and their iodo analogs (2) rea
cted selectively with the sulfhydryl groups generated in a limited red
uction of the hinge disulfide bonds of an immunoglobulin G (IgG) givin
g proteins labeled with a fluorescent and/or radioactive moiety. Quant
itative alkylation of free thiol groups was obtained with 1 and I-125/
127-2. Photodimerization of these adducts produced IgG with covalently
joined heavy chains.