Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.
Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Allianz, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.
Trends Cell Biol. 2015 Oct;25(10):611-622. doi: 10.1016/j.tcb.2015.07.003.
Protein degradation is a fundamentally important process that allows cells to recognize and remove damaged protein species and to regulate protein abundance according to functional need. A fundamental challenge is to understand how membrane proteins are recognized and removed from cellular organelles. While most of our understanding of this mechanism comes from studies on p97/Cdc48-mediated protein dislocation along the endoplasmic reticulum (ER)-associated degradation (ERAD) pathway, recent studies have revealed intramembrane proteolysis to be an additional mechanism that can extract transmembrane segments. Here, we review these two principles in membrane protein degradation and discuss how intramembrane proteolysis, which introduces an irreversible step in protein dislocation, is used to drive regulated protein turnover.
蛋白质降解是一个非常重要的过程,它允许细胞识别和去除受损的蛋白质种类,并根据功能需求调节蛋白质的丰度。一个基本的挑战是了解膜蛋白如何被识别并从细胞细胞器中去除。虽然我们对这一机制的大部分了解来自于 p97/Cdc48 介导的沿内质网(ER)相关降解(ERAD)途径的蛋白易位研究,但最近的研究揭示了跨膜蛋白酶解是一种可以提取跨膜片段的额外机制。在这里,我们回顾了这两种膜蛋白降解的原理,并讨论了跨膜蛋白酶解如何引入蛋白质易位的不可逆步骤,从而驱动调节蛋白周转。