Lithgow T
Russell Grimwade School of Biochemistry and Molecular Biology, University of Melbourne, Vic. 3010, Parkville, Australia.
FEBS Lett. 2000 Jun 30;476(1-2):22-6. doi: 10.1016/s0014-5793(00)01663-x.
A clear picture has emerged over the past years on how a 'classic' mitochondrial protein, like subunit IV of cytochrome c oxidase, might be targeted to mitochondria. The targeting and subsequent import process involves the commitment of the TOM (translocase in the outer mitochondrial membrane) receptor complex on the mitochondrial surface, a TIM (translocase in the inner mitochondrial membrane) translocation complex in the mitochondrial inner membrane, and assorted chaperones and processing enzymes within the organelle. Recent work suggests that while very many mitochondrial precursor proteins might follow this basic targeting pathway, a large number have further requirements if they are to be successfully imported. These include ribosome-associated factors and soluble factors in the cytosol, soluble factors in the mitochondrial intermembrane space, an additional TIM translocase in the inner membrane and a range of narrow specificity assembly factors in the inner membrane. This review is focused on the targeting of proteins up to the stage at which they enter the TOM complex in the outer membrane.
在过去几年里,关于一种“经典”线粒体蛋白,如细胞色素c氧化酶亚基IV,如何被靶向运输到线粒体已形成了清晰的认识。靶向运输及随后的导入过程涉及线粒体表面的TOM(外膜转位酶)受体复合物、线粒体内膜中的TIM(内膜转位酶)转位复合物,以及细胞器内的各种伴侣蛋白和加工酶。最近的研究表明,虽然许多线粒体前体蛋白可能遵循这种基本的靶向运输途径,但如果要成功导入,大量蛋白还有进一步的要求。这些要求包括细胞质中与核糖体相关的因子和可溶性因子、线粒体外膜间隙中的可溶性因子、内膜中的另一种TIM转位酶以及内膜中一系列特异性狭窄的组装因子。本综述聚焦于蛋白质在进入外膜中的TOM复合物之前的靶向运输阶段。