Hanau S, Bertelli M, Dallocchio F, Rippa M
Dipartimento di Biochimica e Biologia Molecolare, Università di Ferrara, Italy.
Biochem Mol Biol Int. 1995 Nov;37(4):785-93.
Bromopyruvate inactivates 6-phosphogluconate dehydrogenase by affinity labeling. Kinetic analyses, stoichiometry and isolation of a single labelled tryptic peptide of the modified protein indicate that inactivation is due to the affinity labeling of a single cysteine residue, identified as cysteine 401. It thus appears that this cysteine is within a short distance from the protein site involved in the binding of the carboxylate group of the substrate. These results suggest that the carboxylate binding site of proteins could be used as an anchorage point for affinity labeling, and that bromopyruvate can be used to individuate an amino acid residue within few A from this site.
溴丙酮酸通过亲和标记使6-磷酸葡萄糖酸脱氢酶失活。动力学分析、化学计量以及对修饰蛋白单个标记胰蛋白酶肽段的分离表明,失活是由于单个半胱氨酸残基的亲和标记,该残基被鉴定为半胱氨酸401。因此,这个半胱氨酸似乎距离参与底物羧基结合的蛋白位点很近。这些结果表明,蛋白质的羧基结合位点可作为亲和标记的固定点,并且溴丙酮酸可用于确定距该位点几埃范围内的一个氨基酸残基。