Membrane Fission: The Biogenesis of Transport Carriers

被引:87
作者
Campelo, Felix [1 ,2 ]
Malhotra, Vivek [1 ,2 ,3 ]
机构
[1] CRG, Dept Cell & Dev Biol, Barcelona 08003, Spain
[2] UPF, Barcelona 08003, Spain
[3] ICREA, Barcelona 08010, Spain
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 81 | 2012年 / 81卷
关键词
dynamin; BAR domain; actin; Sar1; Arf; protein kinase D; PROTEIN-KINASE-D; COATED VESICLE FORMATION; ADP-RIBOSYLATION FACTOR; CLATHRIN-MEDIATED ENDOCYTOSIS; PLECKSTRIN HOMOLOGY DOMAIN; RETICULUM EXIT SITES; PLASMA-MEMBRANE; GOLGI MEMBRANES; LIPID-BILAYERS; CELL-SURFACE;
D O I
10.1146/annurev-biochem-051710-094912
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Membrane-bound transport carriers are used to transfer cargo between membranes of the secretory and the endocytic pathways. The generation of these carriers can be classified into three steps: segregation of cargo away from the residents of a donor compartment (cargo sorting), generation of membrane curvature commensurate with the size of the cargo (membrane budding or tubulation), and finally separation of the nascent carrier from the donor membrane by a scission or membrane fission event. This review summarizes advances in our understanding of some of the best-characterized proteins required for the membrane fission that separates a transport carrier from its progenitor compartment: the large GTPase dynamin, the small guanine nucleotide-binding (G) proteins of the Arf family, BAR (Bin-amphiphysin-Rvs) domain proteins, and protein kinase D. These proteins share their ability to insert into membranes and oligomerize to create the large curvatures; however, the overall process of fission that involves these proteins appears to be quite different.
引用
收藏
页码:407 / 427
页数:21
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