Vincenz-Donnelly Lisa, Hipp Mark S
Max Planck Institute of Biochemistry, Department of Cellular Biochemistry, 82152 Martinsried, Germany.
Free Radic Biol Med. 2017 Jul;108:383-393. doi: 10.1016/j.freeradbiomed.2017.03.031. Epub 2017 Mar 29.
One third of the eukaryotic proteome is synthesized at the endoplasmic reticulum (ER), whose unique properties provide a folding environment substantially different from the cytosol. A healthy, balanced proteome in the ER is maintained by a network of factors referred to as the ER quality control (ERQC) machinery. This network consists of various protein folding chaperones and modifying enzymes, and is regulated by stress response pathways that prevent the build-up as well as the secretion of potentially toxic and aggregation-prone misfolded protein species. Here, we describe the components of the ERQC machinery, investigate their response to different forms of stress, and discuss the consequences of ERQC break-down.
真核生物蛋白质组的三分之一是在内质网(ER)中合成的,内质网的独特性质提供了一个与细胞质有很大不同的折叠环境。内质网中健康、平衡的蛋白质组是由一组被称为内质网质量控制(ERQC)机制的因子网络维持的。这个网络由各种蛋白质折叠伴侣和修饰酶组成,并受应激反应途径调节,这些途径可防止潜在有毒且易于聚集的错误折叠蛋白种类的积累和分泌。在这里,我们描述了ERQC机制的组成部分,研究了它们对不同形式应激的反应,并讨论了ERQC功能障碍的后果。