Protein quality control at the endoplasmic reticulum

被引:109
作者
McCaffrey, Kathleen [1 ]
Braakman, Ineke [1 ]
机构
[1] Univ Utrecht, Cellular Prot Chem, Padualaan 8, NL-3584 CH Utrecht, Netherlands
来源
PROTEOSTASIS | 2016年 / 60卷 / 02期
关键词
ER-ASSOCIATED DEGRADATION; PATHWAY; ATF6-ALPHA;
D O I
10.1042/EBC20160003
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 ER (endoplasmic reticulum) is the protein folding 'factory' of the secretory pathway. Virtually all proteins destined for the plasma membrane, the extracellular space or other secretory compartments undergo folding and maturation within the ER. The ER hosts a unique PQC (protein quality control) system that allows specialized modifications such as glycosylation and disulfide bond formation essential for the correct folding and function of many secretory proteins. It is also the major checkpoint for misfolded or aggregation-prone proteins that may be toxic to the cell or extracellular environment. A failure of this system, due to aging or other factors, has therefore been implicated in a number of serious human diseases. In this article, we discuss several key features of ER PQC that maintain the health of the cellular secretome.
引用
收藏
页码:227 / 235
页数:9
相关论文
共 28 条
[1]   BiP and Its Nucleotide Exchange Factors Grp170 and Sil1: Mechanisms of Action and Biological Functions [J].
Behnke, Julia ;
Feige, Matthias J. ;
Hendershot, Linda M. .
JOURNAL OF MOLECULAR BIOLOGY, 2015, 427 (07) :1589-1608
[2]   Glycan regulation of ER-associated degradation through compartmentalization [J].
Benyair, Ron ;
Ogen-Shtern, Navit ;
Lederkremer, Gerardo Z. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2015, 41 :99-109
[3]   Targeting pathways of C-tail-anchored proteins [J].
Borgese, Nica ;
Fasana, Elisa .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2011, 1808 (03) :937-946
[4]   Cleaning Up: ER-Associated Degradation to the Rescue [J].
Brodsky, Jeffrey L. .
CELL, 2012, 151 (06) :1163-1167
[5]   A sweet code for glycoprotein folding [J].
Caramelo, Julio J. ;
Parodi, Armando J. .
FEBS LETTERS, 2015, 589 (22) :3379-3387
[6]   Distinct ubiquitin-ligase complexes define convergent pathways for the degradation of ER proteins [J].
Carvalho, Pedro ;
Goder, Veit ;
Rapoport, Tom A. .
CELL, 2006, 126 (02) :361-373
[7]   Mechanisms of Integral Membrane Protein Insertion and Folding [J].
Cymer, Florian ;
von Heijne, Gunnar ;
White, Stephen H. .
JOURNAL OF MOLECULAR BIOLOGY, 2015, 427 (05) :999-1022
[8]   Co- and Post-Translational Protein Folding in the ER [J].
Ellgaard, Lars ;
McCaul, Nicholas ;
Chatsisvili, Anna ;
Braakman, Ineke .
TRAFFIC, 2016, 17 (06) :615-638
[9]   Ubiquitin-Dependent Intramembrane Rhomboid Protease Promotes ERAD of Membrane Proteins [J].
Fleig, Lina ;
Bergbold, Nina ;
Sahasrabudhe, Priyanka ;
Geiger, Beate ;
Kaltak, Lejla ;
Lemberg, Marius K. .
MOLECULAR CELL, 2012, 47 (04) :558-569
[10]   Unfolded Proteins Are Ire1-Activating Ligands That Directly Induce the Unfolded Protein Response [J].
Gardner, Brooke M. ;
Walter, Peter .
SCIENCE, 2011, 333 (6051) :1891-1894