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1
Mechanisms of Sec61/SecY-mediated protein translocation across membranes.Sec61/SecY 介导的跨膜蛋白易位的机制。
Annu Rev Biophys. 2012;41:21-40. doi: 10.1146/annurev-biophys-050511-102312. Epub 2011 Dec 16.
2
A calmodulin-dependent translocation pathway for small secretory proteins.钙调蛋白依赖性小分泌蛋白转位途径。
Cell. 2011 Dec 23;147(7):1576-88. doi: 10.1016/j.cell.2011.11.048.
3
Structure, mechanism, and evolution of Ero1 family enzymes.Ero1 家族酶的结构、机制和进化。
Antioxid Redox Signal. 2012 Apr 15;16(8):790-9. doi: 10.1089/ars.2011.4418. Epub 2012 Jan 25.
4
Crosstalk and barriers between the electron carriers of the endoplasmic reticulum.内质网电子载体间的串扰和屏障。
Antioxid Redox Signal. 2012 Apr 15;16(8):772-80. doi: 10.1089/ars.2011.4437. Epub 2012 Jan 18.
5
The protein disulfide isomerase family: key players in health and disease.蛋白质二硫键异构酶家族:健康与疾病的关键因素。
Antioxid Redox Signal. 2012 Apr 15;16(8):781-9. doi: 10.1089/ars.2011.4439. Epub 2012 Jan 25.
6
GRP94: An HSP90-like protein specialized for protein folding and quality control in the endoplasmic reticulum.葡萄糖调节蛋白94:一种在内质网中专门负责蛋白质折叠和质量控制的热休克蛋白90样蛋白。
Biochim Biophys Acta. 2012 Mar;1823(3):774-87. doi: 10.1016/j.bbamcr.2011.10.013. Epub 2011 Nov 3.
7
A systematic study of site-specific GalNAc-type O-glycosylation modulating proprotein convertase processing.一种针对特定位点的 GalNAc 型 O-糖基化调节蛋白原转化酶加工的系统研究。
J Biol Chem. 2011 Nov 18;286(46):40122-32. doi: 10.1074/jbc.M111.287912. Epub 2011 Sep 20.
8
Fringe benefits: functional and structural impacts of O-glycosylation on the extracellular domain of Notch receptors.[标题:神经钙黏蛋白胞外结构域 O-糖基化的功能与结构影响] 附加福利:神经钙黏蛋白受体胞外结构域 O-糖基化对其功能和结构的影响。
Curr Opin Struct Biol. 2011 Oct;21(5):583-9. doi: 10.1016/j.sbi.2011.08.008. Epub 2011 Sep 15.
9
Protein export at the ER: loading big collagens into COPII carriers.内质网中的蛋白输出:将大胶原加载到 COPII 载体中。
EMBO J. 2011 Aug 31;30(17):3475-80. doi: 10.1038/emboj.2011.255.
10
Ero1α regulates Ca(2+) fluxes at the endoplasmic reticulum-mitochondria interface (MAM).Ero1α 调节内质网-线粒体接触位点(MAM)处的 Ca(2+) 流。
Antioxid Redox Signal. 2012 May 15;16(10):1077-87. doi: 10.1089/ars.2011.4004. Epub 2011 Oct 19.

蛋白质分泌与内质网。

Protein secretion and the endoplasmic reticulum.

机构信息

School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, United Kingdom.

出版信息

Cold Spring Harb Perspect Biol. 2012 Aug 1;4(8):a012872. doi: 10.1101/cshperspect.a012872.

DOI:10.1101/cshperspect.a012872
PMID:22700933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3405867/
Abstract

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.

摘要

在复杂的多细胞生物中,不同的细胞类型执行专门的功能,因此,细胞和组织的分泌产物差异很大。有些静止的细胞类型只分泌少量的蛋白质,而像胰腺这样产生胰岛素和其他激素的组织,以及产生抗体的成熟 B 细胞,对它们的内质网(ER)有很高的要求。我们现在对 ER 中一般的蛋白质分泌是如何被控制的有了相当复杂的理解。然而,我们的知识仍然存在空白,特别是在将从模型系统中获得的见解应用于体内更复杂的情况时。本文描述了我们对内质网及其在为分泌准备蛋白质方面的作用的理解的最新进展,重点介绍糖蛋白的质量控制和二硫键形成途径。