Asymmetric Supported Lipid Bilayer Formation via Methyl-β-Cyclodextrin Mediated Lipid Exchange: Influence of Asymmetry on Lipid Dynamics and Phase Behavior

被引:44
|
作者
Visco, Ilaria [1 ]
Chiantia, Salvatore [2 ]
Schwille, Petra [1 ]
机构
[1] Max Planck Inst Biochem, Dept Cellular & Mol Biophys, D-82152 Martinsried, Germany
[2] Humboldt Univ, Dept Biol, D-10115 Berlin, Germany
关键词
GIANT UNILAMELLAR VESICLES; MEMBRANE-PROTEINS; PLASMA-MEMBRANE; FLIP-FLOP; CHOLESTEROL; MIXTURES; DOMAINS; CELLS; RECONSTITUTION; SPECTROSCOPY;
D O I
10.1021/la500468r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Supported lipid bilayers (SLBs) are broadly used as minimal membrane models and commonly produced by vesicle fusion (VF) on solid supports. Despite its advantages, VF does not allow the controlled formation of bilayers that mimic the leaflet asymmetry in lipid composition normally found in biological systems. Here we present a simple, quick, and versatile method to produce SLBs with a desired asymmetric lipid composition which is stable for ca. 4 h. We apply methyl-beta-cyclodextrin mediated lipid exchange to SLBs formed by VF to enrich the upper leaflet of the bilayer with sphingomyelin. The bilayer asymmetry is assessed by fluorescence correlation spectroscopy, measuring the lipid mobility separately in each leaflet. To check the compatibility of the method with the most common protein reconstitution approaches, we report the production of asymmetric SLBs (aSLBs) in the presence of a glycosylphosphatidylinositol-anchored protein, reconstituted in the bilayer both, via direct protein insertion, and via proteoliposomes fusion. We finally apply aSLBs to study phase separation and transbilayer lipid movement of raft-mimicking lipid mixtures. The observed differences in terms of phase separation in symmetric and asymmetric SLBs with the same overall lipid composition provide further experimental evidence that the transversal lipid distribution affects the overall lipid miscibility and allow to temporally investigate leaflet mixing.
引用
收藏
页码:7475 / 7484
页数:10
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