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线粒体AAA蛋白酶——迈向对膜结合蛋白水解机器的分子理解

Mitochondrial AAA proteases--towards a molecular understanding of membrane-bound proteolytic machines.

作者信息

Gerdes Florian, Tatsuta Takashi, Langer Thomas

机构信息

Institute for Genetics, Centre for Molecular Medicine (CMMC), Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Zülpicher Str. 47a, 50674 Cologne, Germany.

出版信息

Biochim Biophys Acta. 2012 Jan;1823(1):49-55. doi: 10.1016/j.bbamcr.2011.09.015. Epub 2011 Oct 6.

Abstract

Mitochondrial AAA proteases play an important role in the maintenance of mitochondrial proteostasis. They regulate and promote biogenesis of mitochondrial proteins by acting as processing enzymes and ensuring the selective turnover of misfolded proteins. Impairment of AAA proteases causes pleiotropic defects in various organisms including neurodegeneration in humans. AAA proteases comprise ring-like hexameric complexes in the mitochondrial inner membrane and are functionally conserved from yeast to man, but variations are evident in the subunit composition of orthologous enzymes. Recent structural and biochemical studies revealed how AAA proteases degrade their substrates in an ATP dependent manner. Intersubunit coordination of the ATP hydrolysis leads to an ordered ATP hydrolysis within the AAA ring, which ensures efficient substrate dislocation from the membrane and translocation to the proteolytic chamber. In this review, we summarize recent findings on the molecular mechanisms underlying the versatile functions of mitochondrial AAA proteases and their relevance to those of the other AAA+ machines.

摘要

线粒体AAA蛋白酶在维持线粒体蛋白质稳态中发挥着重要作用。它们作为加工酶,通过调节和促进线粒体蛋白质的生物合成,并确保错误折叠蛋白质的选择性周转。AAA蛋白酶功能受损会在包括人类神经退行性变在内的各种生物体中导致多效性缺陷。AAA蛋白酶在线粒体内膜中形成环状六聚体复合物,从酵母到人类在功能上具有保守性,但直系同源酶的亚基组成存在明显差异。最近的结构和生化研究揭示了AAA蛋白酶如何以ATP依赖的方式降解其底物。ATP水解的亚基间协同作用导致AAA环内有序的ATP水解,这确保了底物从膜上有效地移位并转运到蛋白水解腔室。在这篇综述中,我们总结了关于线粒体AAA蛋白酶多功能分子机制及其与其他AAA+机器机制相关性的最新研究结果。

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