van der Laan Martin, Wiedemann Nils, Mick David U, Guiard Bernard, Rehling Peter, Pfanner Nikolaus
Institut für Biochemie und Molekularbiologie, Zentrum für Biochemie und Molekulare Zellforschung, Universität Freiburg, Hermann-Herder-Strasse 7, D-79104 Freiburg, Germany.
Curr Biol. 2006 Nov 21;16(22):2271-6. doi: 10.1016/j.cub.2006.10.025.
The mitochondrial inner membrane harbors complexes of the respiratory chain and translocase complexes for preproteins. The membrane potential generated by the respiratory chain is essential for ATP production by the mitochondrial ATP synthase and as a driving force for protein import. It is generally believed that the preprotein translocases just use the membrane potential without getting into physical contact with respiratory-chain complexes. Here, we show that the presequence translocase interacts with the respiratory chain. Tim21, a specific subunit of the sorting-active presequence translocase , recruits proton-pumping respiratory-chain complexes and stimulates preprotein insertion. Thus, the presequence translocase cooperates with the respiratory chain and promotes membrane-potential-dependent protein sorting into the inner mitochondrial membrane. These findings suggest a new coupling mechanism in an energy-transducing membrane.
线粒体内膜含有呼吸链复合物和前体蛋白转位酶复合物。呼吸链产生的膜电位对于线粒体ATP合酶产生ATP至关重要,并且作为蛋白质导入的驱动力。人们普遍认为,前体蛋白转位酶仅利用膜电位,而不与呼吸链复合物进行物理接触。在这里,我们表明前序列转位酶与呼吸链相互作用。Tim21是分选活性前序列转位酶的一个特定亚基,它募集质子泵呼吸链复合物并刺激前体蛋白插入。因此,前序列转位酶与呼吸链协同作用,促进依赖膜电位的蛋白质分选到线粒体内膜中。这些发现提示了能量转换膜中的一种新的偶联机制。