Inhibitors of Protein Translocation Across the ER Membrane

被引:20
作者
Kalies, Kai-Uwe [1 ]
Roemisch, Karin [2 ]
机构
[1] Med Univ Lubeck, Inst Biol, CSCM, D-23538 Lubeck, Germany
[2] Univ Saarland, Fac Nat Sci & Technol 8, Dept Microbiol, D-66123 Saarbrucken, Germany
关键词
antigen cross-presentation; endoplasmic reticulum; ER-associated degradation; membrane protein integration; protein secretion; protein translocation; Sec61; channel; ENDOPLASMIC-RETICULUM MEMBRANE; CELL-ADHESION MOLECULE-1; COTRANSLATIONAL TRANSLOCATION; MYCOBACTERIUM-ULCERANS; SEC61; COMPLEX; CD4; RECEPTOR; APRATOXIN-A; IN-VITRO; CHOLESTEROL; VALINOMYCIN;
D O I
10.1111/tra.12308
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Protein translocation into the endoplasmic reticulum (ER) constitutes the first step of protein secretion. ER protein import is essential in all eukaryotic cells and is particularly critical in fast-growing tumour cells. Thus, the process can serve as target both for potential cancer drugs and for bacterial virulence factors. Inhibitors of protein transport across the ER membrane range from broad-spectrum to highly substrate-specific and can interfere with virtually any stage of this multistep process, and even with transport of endocytosed antigens into the cytosol for cross-presentation.
引用
收藏
页码:1027 / 1038
页数:12
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