Chan S H, Barbour R L
Biochim Biophys Acta. 1976 Jun 8;430(3):426-33. doi: 10.1016/0005-2728(76)90018-9.
(1) The ATPase inhibitior protein has been isolated from rat liver mitochondria in purified form. The molecular weight determined by sodium dodecyl sulfate gel electrophoresis is approximately 9500, and the isoelectric point is 8.9. (2) The protein inhibits both the soluble ATPase and the particle-bound ATPase from rat liver mitochondria. It also inhibits ATPase activities of soluble F1, and inhibitor-depleted submitochondrial particles derived from bovine heart mitochondria. (3) On particle-bound ATPase the inhibitor has its maximal effect if incubated in the presence of Mg2+. ATP at slightly acidic pH. (4) The inhibitor has a minimal effect on Pi-ATP exchange activity in sonicated submitochondrial particles. However, unexpectedly the inhibitor greatly stimules Pi-ATP exchange activity in whole mitochondria while the low ATPase activity of the mitochondria is not affected. The possible mechanism of action of the inhibitor on intact mitochondria is offered.
(1) 已从大鼠肝脏线粒体中以纯化形式分离出ATP酶抑制蛋白。通过十二烷基硫酸钠凝胶电泳测定的分子量约为9500,等电点为8.9。(2) 该蛋白抑制大鼠肝脏线粒体中的可溶性ATP酶和颗粒结合ATP酶。它还抑制可溶性F1的ATP酶活性以及源自牛心脏线粒体的去除抑制剂的亚线粒体颗粒的ATP酶活性。(3) 对于颗粒结合ATP酶,如果在存在Mg2+、ATP且pH略呈酸性的条件下孵育,抑制剂具有最大作用。(4) 该抑制剂对超声处理的亚线粒体颗粒中的磷酸根 - ATP交换活性影响最小。然而,出乎意料的是,该抑制剂极大地刺激了完整线粒体中的磷酸根 - ATP交换活性,而线粒体的低ATP酶活性不受影响。文中提出了该抑制剂对完整线粒体的可能作用机制。