Compartmentalization and Selective Tagging for Disposal of Misfolded Glycoproteins

被引:32
作者
Shenkman, Marina [1 ]
Lederkremer, Gerardo Z. [1 ]
机构
[1] Tel Aviv Univ, Sch Mol Cell Biol & Biotechnol, George Wise Fac Life Sci, IL-69978 Tel Aviv, Israel
基金
以色列科学基金会;
关键词
RETICULUM-ASSOCIATED DEGRADATION; ER-ASSOCIATED DEGRADATION; QUALITY-CONTROL COMPARTMENT; ENDOPLASMIC-RETICULUM; MANNOSIDASE-I; MECHANISTIC INSIGHTS; CONTROL VESICLES; N-GLYCOSYLATION; MOLECULAR-BASIS; PROTEIN;
D O I
10.1016/j.tibs.2019.04.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ability of mammalian cells to correctly identify and degrade misfolded secretory proteins, most of them bearing N-glycans, is crucial for their correct function and survival. An inefficient disposal mechanism results in the accumulation of misfolded proteins and consequent endoplasmic reticulum (ER) stress. N-glycan processing creates a code that reveals the folding status of each molecule, enabling continued folding attempts or targeting of the doomed glycoprotein for disposal. We review here the main steps involved in the accurate processing of unfolded glycoproteins. We highlight recent data suggesting that the processing is not stochastic, but that there is selective accelerated glycan trimming on misfolded glycoprotein molecules.
引用
收藏
页码:827 / 836
页数:10
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