Bauer M F, Hofmann S, Neupert W, Brunner M
Institut für Klinische Chemie, Molekulare Diagnostik und Institut für Klinische Chemie, Akad. Krankenhaus München-Schwabing, D-80804 München, Germany.
Trends Cell Biol. 2000 Jan;10(1):25-31. doi: 10.1016/s0962-8924(99)01684-0.
Import of nuclear-encoded mitochondrial preproteins is mediated by a general translocase in the outer membrane, the TOM complex, and by two distinct translocases in the mitochondrial inner membrane, the TIM23 complex and the TIM22 complex. Both TIM complexes cooperate with the TOM complex but facilitate import of different classes of precursor proteins. Precursors with an N-terminal presequence are imported via the TIM23 complex, whereas mitochondrial carrier proteins require the TIM22 complex for insertion into the inner membrane. This review discusses recent advances in understanding the structure and function of the translocases of the inner membrane and the possible role of Tim proteins in the development of the Mohr-Tranebjaerg syndrome, a mitochondrial disorder leading to neurodegeneration.
核编码的线粒体前体蛋白的导入由外膜中的一种通用转运体TOM复合物以及线粒体内膜中的两种不同转运体TIM23复合物和TIM22复合物介导。这两种TIM复合物都与TOM复合物协同作用,但促进不同类别的前体蛋白的导入。具有N端前序列的前体通过TIM23复合物导入,而线粒体载体蛋白则需要TIM22复合物才能插入内膜。本综述讨论了在内膜转运体的结构和功能理解方面的最新进展,以及Tim蛋白在莫尔-特兰伯格综合征(一种导致神经退行性变的线粒体疾病)发展中的可能作用。