Tokatlidis Kostas
IMBB-FORTH, Vasilika Vouton, GR-711 10 Heraklion-Crete, Greece.
Cell. 2005 Jul 1;121(7):965-7. doi: 10.1016/j.cell.2005.06.019.
In this issue of Cell, show that there is a disulfide relay system in the intermembrane space (IMS) of mitochondria that is comprised of the proteins Mia40 and Erv1. This disulfide relay system promotes the import and oxidative folding of proteins. Oxidized Mia40 traps newly imported proteins through mixed disulfide bridges. Subsequent isomerization of these disulfide bridges allows the imported protein to be folded in the IMS. The reduced Mia40 generated is then reoxidized by the sulfhydryl oxidase Erv1, promoting the next round of disulfide exchange. The new work clarifies the molecular function of Mia40 and reveals Mia40 to be the first physiological substrate for the FAD-linked Erv1.
在本期《细胞》杂志中,研究表明线粒体膜间隙(IMS)中存在一个由蛋白质Mia40和Erv1组成的二硫键中继系统。这个二硫键中继系统促进蛋白质的导入和氧化折叠。氧化型的Mia40通过混合二硫键捕获新导入的蛋白质。随后这些二硫键的异构化使得导入的蛋白质在膜间隙中折叠。生成的还原型Mia40随后被巯基氧化酶Erv1重新氧化,促进下一轮的二硫键交换。这项新研究阐明了Mia40的分子功能,并揭示Mia40是与黄素腺嘌呤二核苷酸(FAD)相连的Erv1的首个生理底物。