Chen W J, Douglas M G
Department of Biochemistry, Southwestern Graduate School of Biomedical Sciences, Dallas, Texas 75235.
J Biol Chem. 1988 Apr 15;263(11):4997-5000.
Post-translational import of the F1-ATPase beta-subunit precursor into isolated mitochondria requires both an energized inner membrane and nucleoside triphosphate hydrolysis on the organelle surface. Nested internal deletions of the F1 beta-precursor which progressively move a 128-residue carboxyl-terminal domain of the protein closer to the amino terminus reveal an abrupt transition between residues 122 and 144 to a form of the protein which is imported in the absence of added ATP. This transition region of the F1 beta-precursor is the same sequence which we have defined in earlier studies is required for formation of a tetramer following in vitro translation of the F1 beta-precursor. These data indicate that part of the requirement for ATP in the import of mitochondrial precursors may be involved in the reorganization of oligomeric species on the membrane surface which are formed following their translation.
F1 - ATP酶β亚基前体向分离的线粒体进行翻译后导入,既需要有活力的内膜,也需要在细胞器表面进行核苷三磷酸水解。F1β前体的嵌套内部缺失逐渐使该蛋白128个残基的羧基末端结构域更靠近氨基末端,结果显示在残基122和144之间突然转变为一种在不添加ATP时也能导入的蛋白形式。F1β前体的这个转变区域与我们在早期研究中定义的序列相同,该序列是F1β前体体外翻译后形成四聚体所必需的。这些数据表明,线粒体前体导入过程中对ATP的部分需求可能参与了膜表面寡聚体物种在翻译后形成的重组过程。