Protein Secretion and the Endoplasmic Reticulum

被引:83
作者
Benham, Adam M. [1 ]
机构
[1] Univ Durham, Sch Biol & Biomed Sci, Durham DH1 3LE, England
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2012年 / 4卷 / 08期
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
SIGNAL RECOGNITION PARTICLE; GLUCOSE GLYCOPROTEIN-GLUCOSYLTRANSFERASE; ELONGATION ARREST ACTIVITY; STRUCTURAL BASIS; QUALITY-CONTROL; THIOL OXIDASE; TRANSBILAYER TRANSLOCATION; LINKED OLIGOSACCHARIDES; DISULFIDE-ISOMERASE; DEFICIENCY LEADS;
D O I
10.1101/cshperspect.a012872
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In a complex multicellular organism, different cell types engage in specialist functions, and as a result, the secretory output of cells and tissues varies widely. Whereas some quiescent cell types secrete minor amounts of proteins, tissues like the pancreas, producing insulin and other hormones, and mature B cells, producing antibodies, place a great demand on their endoplasmic reticulum (ER). Our understanding of how protein secretion in general is controlled in the ER is now quite sophisticated. However, there remain gaps in our knowledge, particularly when applying insight gained from model systems to the more complex situations found in vivo. This article describes recent advances in our understanding of the ER and its role in preparing proteins for secretion, with an emphasis on glycoprotein quality control and pathways of disulfide bond formation.
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页数:16
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