Ehrlich R S, Colman R F
J Biol Chem. 1983 Jun 10;258(11):7079-86.
The three dissimilar subunits of pig heart DPN-dependent isocitrate dehydrogenase, which normally occur in the ratio 2 alpha:1 beta:1 gamma, have been separated by chromatofocusing. The subunits were first dissociated from native enzyme (specific activity, 15-20 units/mg) with minimal unfolding in 2 M urea and chromatofocused in the range pH 8-5 in the presence of 1 M urea. Isolated alpha, beta, and gamma subunits had specific activities of 0.4, 0.04, and less than 0.01 unit/mg, respectively, suggesting that at least 3 of the 4 subunits of the alpha 2 beta gamma tetramer contain elements of the catalytic site. Addition of pairs of subunits to assay mixtures resulted in markedly enhanced activity for alpha plus gamma (specific activity, 7.8 units/mg) and alpha plus beta (2.9 units/mg), but not for beta plus gamma. The subunit concentration dependence of enhanced activity indicated formation of stoichiometric alpha beta and alpha gamma complexes. Sedimentation equilibrium experiments revealed that alpha, as isolated, exists primarily as a dimer, while beta and gamma are monomeric. The combinations of alpha and beta and alpha and gamma are dimers. Under the conditions used, no larger complexes were formed when all 3 subunits were added in the ratio (2 alpha:1 beta:1 gamma) found in native enzyme and these mixtures failed to show increased activity above that found with alpha beta and alpha gamma. Native enzyme exhibits a reduced Km for the substrate, isocitrate, in the presence of ADP, but this allosteric effect was not observed for the isolated subunits or for combinations of alpha with beta or gamma. However, ADP binding to isolated alpha and beta subunits as well as to alpha beta and alpha gamma dimers was only slightly reduced from that of native enzyme. These results indicate that although all subunits may have the elements of the catalytic and allosteric sites, optimum activity and regulatory properties may require the association of dissimilar subunits.
猪心依赖二磷酸吡啶核苷酸(DPN)的异柠檬酸脱氢酶的三种不同亚基,其正常比例为2α:1β:1γ,已通过色谱聚焦法分离。这些亚基首先在2M尿素中以最小程度的解折叠从天然酶(比活性为15 - 20单位/毫克)中解离出来,并在1M尿素存在下于pH 8 - 5范围内进行色谱聚焦。分离得到的α、β和γ亚基的比活性分别为0.4、0.04和小于0.01单位/毫克,这表明α₂βγ四聚体的4个亚基中至少有3个包含催化位点的元素。将成对的亚基添加到测定混合物中,导致α加γ(比活性为7.8单位/毫克)和α加β(2.9单位/毫克)的活性显著增强,但β加γ则不然。增强活性的亚基浓度依赖性表明形成了化学计量的αβ和αγ复合物。沉降平衡实验表明,分离得到的α主要以二聚体形式存在,而β和γ是单体。α与β以及α与γ的组合是二聚体。在所使用的条件下,当以天然酶中发现的比例(2α:1β:1γ)添加所有3个亚基时,没有形成更大的复合物,并且这些混合物的活性没有比αβ和αγ的活性增加。天然酶在ADP存在下对底物异柠檬酸的Km降低,但对于分离的亚基或α与β或γ的组合未观察到这种变构效应。然而,ADP与分离的α和β亚基以及与αβ和αγ二聚体的结合仅比天然酶略有降低。这些结果表明,尽管所有亚基可能都具有催化和变构位点的元素,但最佳活性和调节特性可能需要不同亚基的结合。