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用于前体跨线粒体内膜转运的蛋白质转运机制。

Protein transport machineries for precursor translocation across the inner mitochondrial membrane.

作者信息

Wagner Karina, Mick David U, Rehling Peter

机构信息

Institut für Biochemie und Molekularbiologie, ZBMZ, Universität Freiburg, D-79104 Freiburg, Germany.

出版信息

Biochim Biophys Acta. 2009 Jan;1793(1):52-9. doi: 10.1016/j.bbamcr.2008.05.026. Epub 2008 Jun 11.

Abstract

The mitochondrial inner membrane has a central function for the energy metabolism of the cell. The respiratory chain generates a proton gradient across the inner mitochondrial membrane, which is used to produce ATP by the F1Fo-ATPase. To maintain the electrochemical gradient, the inner membrane represents an efficient permeability barrier for small molecules. Nevertheless, metabolites as well as polypeptide chains need to be transported across the inner membrane while the electrochemical gradient is retained. While specialized metabolite carrier proteins mediate the transport of small molecules, dedicated protein translocation machineries in the inner mitochondrial membrane (so called TIM complexes) transport precursor proteins across the inner membrane. Here we describe the organization of the TIM complexes and discuss the current models as to how they mediate the posttranslational import of proteins across and into the inner mitochondrial membrane.

摘要

线粒体内膜对细胞的能量代谢起着核心作用。呼吸链在跨线粒体内膜产生质子梯度,该质子梯度被F1Fo - ATP合酶用于生成ATP。为维持电化学梯度,内膜对小分子而言是一道有效的通透屏障。然而,代谢物以及多肽链需要在保持电化学梯度的同时跨内膜转运。虽然专门的代谢物载体蛋白介导小分子的转运,但线粒体内膜中专门的蛋白质转运机制(即所谓的TIM复合物)则将前体蛋白转运过内膜。在此,我们描述TIM复合物的组成,并讨论当前关于它们如何介导蛋白质跨线粒体内膜进行翻译后导入及进入内膜的模型。

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