Mollinedo F, Larraga V, Coll F J, Muñoz E
Biochem J. 1980 Mar 15;186(3):713-23. doi: 10.1042/bj1860713.
An energy-transducing adenosine triphosphatase (ATPase, EC 3.6.1.3) that contains an extra polypeptide (delta) as well as three intrinsic subunits (alpha, beta, gamma) was purified from Micrococcus lysodeikticus membranes. The apparent subunit stoichiometry of this soluble ATPase complex is alpha 3 beta 3 gamma delta. The functional role of the subunits was studied by correlating subunit sensitivity to trypsin and effect of antibodies raised against holo-ATPase and its alpha, beta and gamma subunits with changes in ATPase activity and ATPase rebinding to membranes. A form of the ATPase with the subunit proportions 1.67(alpha):3.00(beta:0.17(gamma) was isolated after trypsin treatment of purified ATPase. This form has more than twice the specific activity of native enzyme. Other forms with less relative proportion of alpha subunits and absence of gamma subunit are not active. Of the antisera to subunits, only anti-(beta-subunit) serum shows a slight inhibitory effect on ATPase activity, but its combination with either anti-(alpha-subunit) or anti-(gamma-subunit) serum increases the effect. The results suggest that beta subunit is required for full ATPase activity, although a minor proportion of alpha and perhaps gamma subunit(s) is also required, probably to impart an active conformation to the protein. The additional polypeptide not hitherto described in Micrococcus lysodeikticus ATPase had a molecular weight of 20 000 and was found to be involved in ATPase binding to membranes. This 20 000-dalton component can be equated with the delta subunit of other energy-transducing ATPases and its association with the (alpha, beta, gamma) M. lysodeikticus ATPase complex appears to be dependent on bivalent cations. The present results do not preclude the possibility that the gamma subunit also plays a role in ATPase binding, in which, however, the major subunits do not seem to play a role.
从溶壁微球菌膜中纯化出一种能量转换型三磷酸腺苷酶(ATP酶,EC 3.6.1.3),它含有一条额外的多肽(δ)以及三个固有亚基(α、β、γ)。这种可溶性ATP酶复合物的亚基化学计量比明显为α3β3γδ。通过将亚基对胰蛋白酶的敏感性以及针对全酶ATP酶及其α、β和γ亚基产生的抗体的作用与ATP酶活性变化和ATP酶与膜的重新结合相关联,研究了这些亚基的功能作用。用胰蛋白酶处理纯化的ATP酶后,分离出一种亚基比例为1.67(α):3.00(β):0.17(γ)的ATP酶形式。这种形式的比活性是天然酶的两倍多。其他α亚基相对比例较低且没有γ亚基的形式没有活性。在针对亚基的抗血清中,只有抗(β亚基)血清对ATP酶活性有轻微抑制作用,但其与抗(α亚基)或抗(γ亚基)血清结合会增强这种作用。结果表明,β亚基是ATP酶充分发挥活性所必需的,尽管可能还需要少量的α亚基和γ亚基,可能是为了赋予蛋白质活性构象。溶壁微球菌ATP酶中迄今未描述的额外多肽分子量为20000,发现它参与ATP酶与膜的结合。这个20000道尔顿的组分可等同于其他能量转换型ATP酶的δ亚基及其与溶壁微球菌ATP酶(α、β、γ)复合物的结合似乎依赖于二价阳离子。目前的结果并不排除γ亚基在ATP酶结合中也起作用的可能性,然而在这方面主要亚基似乎不起作用。