Hodges C T, Wiggins J C, Harrison J H
J Biol Chem. 1977 Sep 10;252(17):6038-41.
The pH-dependent dissociation of porcine heart mitochondrial malate dehydrogenase (L-malate:NAD+ oxidoreductase, EC 1.1.1.37) has been further characterized using the technique of sedimentation velocity ultracentrifugation. The increased rate and specificity of the inactivation of mitochondrial malate dehydrogenase by the sulfhydryl reagent N-ethylmaleimide has been correlated with the pH-dependent dissociation of the enzyme. Data obtained using NAD+ and its component parts to reassociate the enzyme and also to protect the enzyme from inactivation by N-ethylmaleimide suggest that the sulfhydryl residues being modified by N-ethylmaleimide are inaccessible when the enzyme is in its dimeric form. A dissociation curve for the pH-dependent dissociation suggests that a limited number of residues are being protonated concomitant with dissociation of the enzyme. An apparent pKa of 5.3 has been determined for this phenomenon. Studies using enzyme modified by the sulfhydryl reagent N-ethylmaleimide indicate that selective modification of essential sulfhydryl residues alters the proper binding of NADH.
运用沉降速度超速离心技术,对猪心脏线粒体苹果酸脱氢酶(L-苹果酸:NAD⁺氧化还原酶,EC 1.1.1.37)的pH依赖性解离进行了进一步表征。巯基试剂N-乙基马来酰亚胺使线粒体苹果酸脱氢酶失活的速率和特异性增加,这与该酶的pH依赖性解离相关。使用NAD⁺及其组成部分使酶重新缔合以及保护酶不被N-乙基马来酰亚胺失活所获得的数据表明,当酶处于二聚体形式时,被N-乙基马来酰亚胺修饰的巯基残基无法接近。pH依赖性解离的解离曲线表明,随着酶的解离,有限数量的残基正在被质子化。已确定此现象的表观pKa为5.3。使用经巯基试剂N-乙基马来酰亚胺修饰的酶进行的研究表明,对必需巯基残基的选择性修饰会改变NADH的正确结合。