Sorting of Lipids and Proteins in Membrane Curvature Gradients

被引:244
作者
Tian, A. [1 ,2 ]
Baumgart, T. [1 ]
机构
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
BENDING STIFFNESS; TETHER FORMATION; BILAYER-MEMBRANE; CELL-MEMBRANE; CHOLERA-TOXIN; PHOSPHOLIPID-MEMBRANES; ERYTHROCYTE-MEMBRANE; PHASE-SEPARATION; EXTENSIONAL FLOW; PLASMA-MEMBRANE;
D O I
10.1016/j.bpj.2008.11.067
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The sorting of lipids and proteins in cellular trafficking pathways is a process of central importance in maintaining compartmentalization in eukaryotic cells. However, the mechanisms behind these sorting phenomena are currently far from being understood. Among several mechanistic suggestions, membrane curvature has been invoked as a means to segregate lipids and proteins in cellular sorting centers. To assess this hypothesis, we investigate the sorting of lipid analog dye trace components between highly curved tubular membranes and essentially flat membranes of giant unilamellar vesicles. Our experimental findings indicate that intracellular lipid sorting, contrary to frequent assumptions, is unlikely to occur by lipids fitting into membrane regions of appropriate curvature. This observation is explained in the framework of statistical mechanical lattice models that show that entropy, rather than curvature energy, dominates lipid distribution in the absence of strongly preferential lateral intermolecular interactions. Combined with previous findings of curvature induced phase segregation, we conclude that lipid cooperativity is required to enable efficient sorting. In contrast to lipid analog dyes, the peripheral membrane binding protein Cholera toxin subunit B is effectively curvature-sorted. The sorting of Cholera toxin subunit B is rationalized by statistical models. We discuss the implications of our findings for intracellular sorting mechanisms.
引用
收藏
页码:2676 / 2688
页数:13
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