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线粒体蛋白质导入机制的多功能性。

Versatility of the mitochondrial protein import machinery.

作者信息

Pfanner N, Geissler A

机构信息

Institut für Biochemie und Molekularbiologie, Universität Freiburg, Hermann-Herder-Strasse 7, D-79104 Freiburg, Germany.

出版信息

Nat Rev Mol Cell Biol. 2001 May;2(5):339-49. doi: 10.1038/35073006.

Abstract

The vast majority of mitochondrial proteins are synthesized in the cytosol and are imported into mitochondria by protein machineries located in the mitochondrial membranes. It has become clear that hydrophilic as well as hydrophobic preproteins use a common translocase in the outer mitochondrial membrane, but diverge to two distinct translocases in the inner membrane. The translocases are dynamic, high-molecular-weight complexes that have to provide specific means for the recognition of preproteins, channel formation and generation of import-driving forces.

摘要

绝大多数线粒体蛋白在细胞质中合成,然后通过位于线粒体膜上的蛋白质机制导入线粒体。目前已经明确,亲水性和疏水性前体蛋白在外膜使用共同的转位酶,但在内膜则分为两种不同的转位酶。这些转位酶是动态的高分子量复合物,必须提供识别前体蛋白、形成通道以及产生导入驱动力的特定方式。

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