Quality control at the plasma membrane: One mechanism does not fit all

被引:53
作者
Babst, Markus [1 ]
机构
[1] Univ Utah, Dept Biol, Ctr Cell & Genome Sci, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
YEAST URACIL PERMEASE; TRANSMEMBRANE CONDUCTANCE REGULATOR; MULTIVESICULAR BODY PATHWAY; K63-LINKED UBIQUITIN CHAINS; DEPENDENT DOWN-REGULATION; AIRWAY EPITHELIAL-CELLS; DEUBIQUITINATING ENZYME; MEDIATE UBIQUITINATION; CONTROL DEGRADATION; PROTEIN-TURNOVER;
D O I
10.1083/jcb.201310113
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The plasma membrane quality control system of eukaryotic cells is able to recognize and degrade damaged cell surface proteins. Recent studies have identified two mechanisms involved in the recognition of unfolded transmembrane proteins. One system uses chaperones to detect unfolded cytoplasmic domains of transmembrane proteins, whereas the second mechanism relies on an internal quality control system of the protein, which can trigger degradation when the protein deviates from the folded state. Both quality control mechanisms are key to prevent proteotoxic effects at the cell surface and to ensure cell integrity.
引用
收藏
页码:11 / 20
页数:10
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