Bihlmaier Karl, Mesecke Nikola, Kloeppel Christine, Herrmann Johannes M
Cell Biology, University of Kaiserslautern, Kaiserslautern, Germany.
Ann N Y Acad Sci. 2008 Dec;1147:293-302. doi: 10.1196/annals.1427.005.
The intermembrane space of mitochondria contains many proteins that lack classical mitochondrial targeting sequences. Instead, these proteins often show characteristic patterns of cysteine residues that are critical for their accumulation in the organelle. Import of these proteins is catalyzed by two essential components, Mia40 and Erv1. Mia40 is a protein in the intermembrane space that directly binds newly imported proteins via disulfide bonds. By reorganization of these bonds, intramolecular disulfide bonds are formed in the imported proteins, which are thereby released from Mia40 into the intermembrane space. Because folded proteins are unable to traverse the import pore of the outer membrane, this leads to a permanent location of these proteins within the mitochondria. During this reaction, Mia40 becomes reduced and needs to be re-oxidized to regain its activity. Oxidation of Mia40 is carried out by Erv1, a conserved flavine adenine dinucleotide (FAD)-binding sulfhydryl oxidase. Erv1 directly interacts with Mia40 and shuttles electrons from reduced Mia40 to oxidized cytochrome c, from whence they flow through cytochrome oxidase to molecular oxygen. The connection of the disulfide relay with the respiratory chain not only significantly increases the efficiency of the oxidase activity, but also prevents the formation of potentially deleterious hydrogen peroxide. The oxidative activity of Erv1 strongly depends on the oxygen concentration in mitochondria. Erv1, therefore, may function as a molecular switch that adapts mitochondrial activities to the oxygen levels in the cell.
线粒体膜间隙包含许多缺乏经典线粒体靶向序列的蛋白质。相反,这些蛋白质常常呈现出特定的半胱氨酸残基模式,这些模式对于它们在细胞器中的积累至关重要。这些蛋白质的导入由两个必需成分Mia40和Erv1催化。Mia40是膜间隙中的一种蛋白质,它通过二硫键直接结合新导入的蛋白质。通过这些键的重新排列,在导入的蛋白质中形成分子内二硫键,从而使这些蛋白质从Mia40释放到膜间隙中。由于折叠的蛋白质无法穿过外膜的导入孔,这导致这些蛋白质在线粒体内永久定位。在这个反应过程中,Mia40被还原,需要重新氧化以恢复其活性。Mia40的氧化由Erv1进行,Erv1是一种保守的黄素腺嘌呤二核苷酸(FAD)结合巯基氧化酶。Erv1直接与Mia40相互作用,并将电子从还原的Mia40穿梭到氧化的细胞色素c,然后电子从细胞色素c流经细胞色素氧化酶传递给分子氧。二硫键传递与呼吸链的连接不仅显著提高了氧化酶活性的效率,还防止了潜在有害的过氧化氢的形成。Erv1的氧化活性强烈依赖于线粒体中的氧气浓度。因此,Erv1可能作为一种分子开关,使线粒体活动适应细胞内的氧气水平。