Naoé Mari, Ohwa Yukimasa, Ishikawa Daigo, Ohshima Chié, Nishikawa Shuh-Ichi, Yamamoto Hayashi, Endo Toshiya
Department of Chemistry, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya 464-8602, Japan.
J Biol Chem. 2004 Nov 12;279(46):47815-21. doi: 10.1074/jbc.M410272200. Epub 2004 Sep 13.
Most mitochondrial proteins are synthesized in the cytosol, imported into mitochondria, and sorted to one of the four mitochondrial subcompartments. Here we identified a new inner membrane protein, Tim40, that mediates sorting of small Tim proteins to the intermembrane space. Tim40 is essential for yeast cell growth, and its function in vivo requires six conserved Cys residues but not anchoring of the protein to the inner membrane by its N-terminal hydrophobic segment. Depletion of Tim40 impairs the import of small Tim proteins into mitochondria both in vivo and in vitro. In wild-type mitochondria, Tim40 forms a translocation intermediate with small Tim proteins prior to their assembly in the intermembrane space in vitro. These results suggest the essential role of Tim40 in sorting/assembly of small Tim proteins.
大多数线粒体蛋白在细胞质中合成,导入线粒体,并被分选到四个线粒体亚区室之一。在这里,我们鉴定出一种新的内膜蛋白Tim40,它介导小Tim蛋白分选到膜间隙。Tim40对酵母细胞生长至关重要,其在体内的功能需要六个保守的半胱氨酸残基,但不需要该蛋白通过其N端疏水片段锚定在内膜上。Tim40的缺失在体内和体外均损害小Tim蛋白导入线粒体。在野生型线粒体中,Tim40在体外小Tim蛋白组装到膜间隙之前与它们形成转位中间体。这些结果表明Tim40在小Tim蛋白的分选/组装中起重要作用。