A sub-nanometre view of how membrane curvature and composition modulate lipid packing and protein recruitment

被引:201
|
作者
Vanni, Stefano [1 ,2 ]
Hirose, Hisaaki [1 ,2 ]
Barelli, Helene [1 ,2 ]
Antonny, Bruno [1 ,2 ]
Gautier, Romain [1 ,2 ]
机构
[1] Univ Nice Sophia Antipolis, Inst Pharmacol Mol & Cellulaire, F-06560 Valbonne, France
[2] CNRS, UMR 7275, F-06560 Valbonne, France
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; AMPHIPATHIC HELICES; BAR DOMAINS; ARFGAP1; MOTIFS; BILAYER; SHAPE; MECHANISM; REVEALS; STRESS;
D O I
10.1038/ncomms5916
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Two parameters of biological membranes, curvature and lipid composition, direct the recruitment of many peripheral proteins to cellular organelles. Although these traits are often studied independently, it is their combination that generates the unique interfacial properties of cellular membranes. Here, we use a combination of in vivo, in vitro and in silico approaches to provide a comprehensive map of how these parameters modulate membrane adhesive properties. The correlation between the membrane partitioning of model amphipathic helices and the distribution of lipid-packing defects in membranes of different shape and composition explains how macroscopic membrane properties modulate protein recruitment by changing the molecular topography of the membrane interfacial region. Furthermore, our results suggest that the range of conditions that can be obtained in a cellular context is remarkably large because lipid composition and curvature have, under most circumstances, cumulative effects.
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页数:10
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