1] Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK. [2].
1] Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA. [2].
Nat Struct Mol Biol. 2014 Apr;21(4):325-35. doi: 10.1038/nsmb.2793.
The eukaryotic endoplasmic reticulum (ER) maintains protein homeostasis by eliminating unwanted proteins through the evolutionarily conserved ER-associated degradation (ERAD) pathway. During ERAD, maturation-defective and surplus polypeptides are evicted from the ER lumen and/or lipid bilayer through the process of retrotranslocation and ultimately degraded by the proteasome. An integral facet of the ERAD mechanism is the ubiquitin system, composed of the ubiquitin modifier and the factors for assembling, processing and binding ubiquitin chains on conjugated substrates. Beyond simply marking polypeptides for degradation, the ubiquitin system is functionally intertwined with retrotranslocation machinery to transport polypeptides across the ER membrane.
真核细胞内质网(ER)通过进化上保守的内质网相关降解(ERAD)途径消除不需要的蛋白质来维持蛋白质的平衡。在 ERAD 过程中,通过逆向转运,不成熟和多余的多肽从 ER 腔和/或脂双层中逐出,并最终被蛋白酶体降解。ERAD 机制的一个重要方面是泛素系统,它由泛素修饰酶和组装、加工和结合连接在共轭底物上的泛素链的因子组成。泛素系统的功能不仅在于简单地标记多肽进行降解,还与逆向转运机制相互交织,以将多肽穿过 ER 膜运输。