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转运体在蛋白质导入线粒体(双膜包被细胞器)过程中的功能协作与分工。

Functional cooperation and separation of translocators in protein import into mitochondria, the double-membrane bounded organelles.

作者信息

Endo Toshiya, Yamamoto Hayashi, Esaki Masatoshi

机构信息

Department of Chemistry, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya 464-8602, Japan.

出版信息

J Cell Sci. 2003 Aug 15;116(Pt 16):3259-67. doi: 10.1242/jcs.00667.

Abstract

Nearly all mitochondrial proteins are synthesized in the cytosol and subsequently imported into mitochondria with the aid of translocators: the TOM complex in the outer membrane, and the TIM23 and TIM22 complexes in the inner membrane. The TOM complex and the TIM complexes cooperate to achieve efficient transport of proteins to the matrix or into the inner membrane and several components, including Tom22, Tim23, Tim50 and small Tim proteins, mediate functional coupling of the two translocator systems. The TOM complex can be disconnected from the TIM systems and their energy sources (ATP and DeltaPsi), however, using alternative mechanisms to achieve vectorial protein translocation across the outer membrane

摘要

几乎所有线粒体蛋白都在细胞质中合成,随后借助转运体导入线粒体:外膜中的TOM复合体,以及内膜中的TIM23和TIM22复合体。TOM复合体和TIM复合体协同作用,以实现蛋白质向基质或内膜的高效转运,包括Tom22、Tim23、Tim50和小Tim蛋白在内的几个组分介导了这两个转运体系统的功能偶联。然而,TOM复合体可以与TIM系统及其能量来源(ATP和ΔΨ)分离,通过其他机制实现蛋白质跨外膜的定向转运

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