Effect of temperature on the formation of liquid phase-separating giant unilamellar vesicles (GUV)

被引:15
作者
Betaneli, Viktoria [1 ]
Worch, Remigiusz [1 ,2 ]
Schwille, Petra [1 ]
机构
[1] Tech Univ Dresden, Biophys Res Grp, BIOTEC, D-01307 Dresden, Germany
[2] Polish Acad Sci, Inst Phys, Phys Biol Lab, PL-02668 Warsaw, Poland
关键词
Giant unilamellar vesicles; Protein reconstitution; Lipid rafts; Confocal microscopy; Fluorescence correlation spectroscopy; Lipid fluorescent probe; LIPID RAFTS; LATERAL DIFFUSION; MODEL; CHOLESTEROL; PROTEIN; PHOSPHOLIPIDS; MIXTURES; RELEVANT; DIAGRAMS;
D O I
10.1016/j.chemphyslip.2012.06.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Giant unilamellar vesicles (GUVs) are widely used as model systems to study both, lipid and membrane protein behavior. During their preparation by the commonly applied electroformation method, a number of issues must be considered to avoid the production of artifacts due to a poor lipid hydration and protein degradation. Here we focus on the effect of preparation temperature on GUVs composed of the most commonly used domain-forming mixture dioleoylelphospatidylcholine/shingomyelin/cholesterol (DOPC/SM/chol) (2/2/1). Lower production temperatures are generally preferable when aiming at a functional reconstitution of proteins into the membrane. On the other hand, lower growth temperature is suspected to alter the lipid composition and the yield of phase-separating vesicles. By confocal imaging, we find that vesicles prepared significantly above and below the melting temperature T-m have the same overall morphology, similar size distributions of vesicles and a similar area coverage by liquid-ordered (L-o) domains. However, a large population analysis indeed reveals a different overall yield of phase-separating vesicles. Two-focus scanning fluorescence correlation spectroscopy measurements did not show any divergence of lipid analog mobility in (L-o) and (L-d) phases in vesicles prepared at different temperatures, indicating that the lowered growth temperature did not influence the lipid organization within the two phases. Moreover, the expected advantages of lower preparation temperature for proteo-GUVs could be exemplified by the reconstitution of voltage dependent anion channel (VDAC) into DOPC/SM/chol GUVs, which aggregates at high, but not at low preparation temperatures. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:630 / 637
页数:8
相关论文
共 39 条
[1]   A Simple Thermodynamic Model of the Liquid-Ordered State and the Interactions between Phospholipids and Cholesterol [J].
Almeida, Paulo F. .
BIOPHYSICAL JOURNAL, 2011, 100 (02) :420-429
[2]   Thermodynamics of lipid interactions in complex bilayers [J].
Almeida, Paulo F. F. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2009, 1788 (01) :72-85
[3]   PERCOLATION AND DIFFUSION IN 3-COMPONENT LIPID BILAYERS - EFFECT OF CHOLESTEROL ON AN EQUIMOLAR MIXTURE OF 2 PHOSPHATIDYLCHOLINES [J].
ALMEIDA, PFF ;
VAZ, WLC ;
THOMPSON, TE .
BIOPHYSICAL JOURNAL, 1993, 64 (02) :399-412
[4]   LIPOSOME ELECTROFORMATION [J].
ANGELOVA, MI ;
DIMITROV, DS .
FARADAY DISCUSSIONS, 1986, 81 :303-+
[5]   The Role of Lipids in VDAC Oligomerization [J].
Betaneli, Viktoria ;
Petrov, Eugene P. ;
Schwille, Petra .
BIOPHYSICAL JOURNAL, 2012, 102 (03) :523-531
[6]   Asymmetry determines the effects of natural ceramides on model membranes [J].
Carrer, Dolores C. ;
Kummer, Eva ;
Chwastek, Grzegorz ;
Chiantia, Salvatore ;
Schwille, Petra .
SOFT MATTER, 2009, 5 (17) :3279-3286
[7]   Model membrane systems and their applications [J].
Chan, Yee-Hung M. ;
Boxer, Steven G. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2007, 11 (06) :581-587
[8]   Lipid rafts reconstituted in model membranes [J].
Dietrich, C ;
Bagatolli, LA ;
Volovyk, ZN ;
Thompson, NL ;
Levi, M ;
Jacobson, K ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2001, 80 (03) :1417-1428
[9]   EVIDENCE FOR METASTABILITY IN STEAROYLSPHINGOMYELIN BILAYERS [J].
ESTEP, TN ;
CALHOUN, WI ;
BARENHOLZ, Y ;
BILTONEN, RL ;
SHIPLEY, GG ;
THOMPSON, TE .
BIOCHEMISTRY, 1980, 19 (01) :20-24
[10]   Phase diagrams and lipid domains in multicomponent lipid bilayer mixtures [J].
Feigenson, Gerald W. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2009, 1788 (01) :47-52