Preparation of bromo[1- 14C]acetyl-coenzyme A as an affinity label for acetyl-coenzyme A binding sites

Abstract

Bromo[1- 14C]acetyl-CoA has been prepared from CoASH and the N-hydroxysuccinimide ester of bromo[1- 14C]acetic acid, and unlabeled bromoacetyl-CoA by reaction of CoASH with bromoacetyl bromide. The products were purified by high-pressure liquid chromatography. Purified bromoacetyl-CoA was characterized, and found to be a potent alkylating agent with a substantial stability in aqueous solution: it decomposed at 30°C and pH 6.6 and 8.0 with halftimes of 3.3 and 2.5 h, respectively. The major breakdown products were CoASH and CoAS · CO · CH 2 · SCoA. Bromo[1- 14C]acetyl-CoA has been used to affinity label the acetyl-CoA binding site of 3-hydroxy-3-methylglutaryl-CoA synthase from ox liver. It was found to irreversibly inhibit the enzyme activity and bind covalently with a stoichiometry for complete inhibition of about 0.8 mol/mol enzyme dimer.