Interplay of proteins and lipids in generating membrane curvature

被引:169
作者
Graham, Todd R. [1 ]
Kozlov, Michael M. [2 ]
机构
[1] Vanderbilt Univ, Dept Biol Sci, Nashville, TN 37235 USA
[2] Tel Aviv Univ, Sackler Fac Med, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
基金
以色列科学基金会;
关键词
P-TYPE ATPASE; PHOSPHOLIPID FLIPPASES; BIOLOGICAL-MEMBRANES; ELASTIC PROPERTIES; VESICLE FORMATION; TUBULE FORMATION; GOLGI; FUSION; BAR; MECHANISMS;
D O I
10.1016/j.ceb.2010.05.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The majority of intracellular membranes have strongly bent shapes with radii of curvature ranging from 20 to 50 nm. Many different proteins provide the substantial energy needed to generate and sustain this curvature. One of the most effective mechanisms of curvature creation is based on asymmetry of membrane monolayers. Proteins generate this asymmetry by flipping phospholipid across the membrane, modifying lipid molecules, or embedding their hydrophobic domains into the membrane matrix. We review the physical principles of these mechanisms of membrane bending and highlight the action of specific proteins driving vesicle-mediated transport. A model of clathrin-mediated vesicle budding from the trans-Golgi network is described to illustrate the interplay and mutual reinforcement of different mechanisms for generating membrane curvature.
引用
收藏
页码:430 / 436
页数:7
相关论文
共 51 条
[1]   N-terminal hydrophobic residues of the G-protein ADP-ribosylation factor-1 insert into membrane phospholipids upon GDP to GTP exchange [J].
Antonny, B ;
BeraudDufour, S ;
Chardin, P ;
Chabre, M .
BIOCHEMISTRY, 1997, 36 (15) :4675-4684
[2]   Membrane curvature induced by Arf1-GTP is essential for vesicle formation [J].
Beck, Rainer ;
Sun, Zhe ;
Adolf, Frank ;
Rutz, Chistoph ;
Bassler, Jochen ;
Wild, Klemens ;
Sinning, Irmgard ;
Hurt, Ed ;
Bruegger, Britta ;
Bethune, Julien ;
Wieland, Felix .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (33) :11731-11736
[3]   Phospholipase A2 (PLA2) enzymes in membrane trafficking:: Mediators of membrane shape and function [J].
Brown, WJ ;
Chambers, K ;
Doody, A .
TRAFFIC, 2003, 4 (04) :214-221
[4]  
CAMPELO F, 2009, FEBS LETT
[5]   The hydrophobic insertion mechanism of membrane curvature generation by proteins [J].
Campelo, Felix ;
McMahon, Harvey T. ;
Kozlov, Michael M. .
BIOPHYSICAL JOURNAL, 2008, 95 (05) :2325-2339
[6]   The Arf activator Gea2p and the P-type ATPase Drs2p interact at the golgi in Saccharomyces cerevisiae [J].
Chantalat, S ;
Park, SK ;
Hua, ZL ;
Liu, K ;
Gobin, R ;
Peyroche, A ;
Rambourg, A ;
Graham, TR ;
Jackson, CL .
JOURNAL OF CELL SCIENCE, 2004, 117 (05) :711-722
[7]   Role for Drs2p, a P-type ATPase and potential aminophospholipid translocase, in yeast late Golgi function [J].
Chen, CY ;
Ingram, MF ;
Rosal, PH ;
Graham, TR .
JOURNAL OF CELL BIOLOGY, 1999, 147 (06) :1223-1236
[8]   Protein-lipid interplay in fusion and fission of biological membranes [J].
Chernomordik, LV ;
Kozlov, MM .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :175-207
[9]   Localization, Purification, and Functional Reconstitution of the P4-ATPase Atp8a2, a Phosphatidylserine Flippase in Photoreceptor Disc Membranes [J].
Coleman, Jonathan A. ;
Kwok, Michael C. M. ;
Molday, Robert S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (47) :32670-32679
[10]   Phospholipid flippases [J].
Daleke, David L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (02) :821-825