Atomic force microscopy of nanometric liposome adsorption and nanoscopic membrane domain formation

被引:82
作者
Tokumasu, F
Jin, AJ
Feigenson, GW
Dvorak, JA
机构
[1] NIAID, Lab Malaria & Vestor Res, Biochem & Biophys Parasitol Sect, NIH, Bethesda, MD 20892 USA
[2] NIH, Off Director, ORS, Div Bioengn & Phys Sci, Bethesda, MD 20892 USA
[3] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
atomic force microscopy (AFM); membrane domain; raft; membrane fusion; surface interaction; phase transition; phase behavior; phospholipids; cholesterol;
D O I
10.1016/S0304-3991(03)00046-9
中图分类号
TH742 [显微镜];
学科分类号
摘要
Scanning probe microscopy studies of membrane fusion and nanoscopic structures were performed using hydrated single lipids and lipid mixtures. Extruded vesicles of DMPC and mixtures at various concentrations of DLPC, DPPC and cholesterol were deposited on freshly cleaved mica and studied in a fluid environment by AFM. The nanostructures formed by these extruded liposomes ranged from isolated unilamellar vesicles to flat sheet membranes and were marked influenced by thermodynamic phase behavior. For DMPC membrane, intact bilayers exhibited a phase transition process in agreement with large bilayer patches. In the DLPC, DPPC and cholesterol mixtures, nanoscopic domain diameters ranged from similar to 25 to 48 nm with height differences of similar to 1.4 nm; all values were lipid composition-dependent. Our data support and extend previous studies of microscopic domains and phase boundaries of the same mixtures in giant unilamellar vesicles determined by confocal light microscopy. Our approach for preparing and utilizing supported membrane structures is potentially relevant to studies of native cell membranes. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:217 / 227
页数:11
相关论文
共 35 条
[1]   Cell biology - A role for lipid shells in targeting proteins to caveolae, rafts, and other lipid domains [J].
Anderson, RGW ;
Jacobson, K .
SCIENCE, 2002, 296 (5574) :1821-1825
[2]  
[Anonymous], 1998, LONG CIRCULATING LIP
[3]   X-RAY STANDING WAVES - A MOLECULAR YARDSTICK FOR BIOLOGICAL-MEMBRANES [J].
BEDZYK, MJ ;
BILDERBACK, DH ;
BOMMARITO, GM ;
CAFFREY, M ;
SCHILDKRAUT, JS .
SCIENCE, 1988, 241 (4874) :1788-1791
[4]   A novel strategy for the preparation of liposomes: rapid solvent exchange [J].
Buboltz, JT ;
Feigenson, GW .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1417 (02) :232-245
[5]   LIPIDAT - A DATABASE OF LIPID PHASE-TRANSITION TEMPERATURES AND ENTHALPY CHANGES - DMPC DATA SUBSET ANALYSIS [J].
CAFFREY, M ;
HOGAN, J .
CHEMISTRY AND PHYSICS OF LIPIDS, 1992, 61 (01) :1-109
[6]   A POSSIBLE MECHANISM FOR VESICLE FORMATION BY EXTRUSION [J].
CLERC, SG ;
THOMPSON, TE .
BIOPHYSICAL JOURNAL, 1994, 67 (01) :475-476
[7]  
DAMMANN B, 1996, HDB NONMEDICAL APPL, P85
[8]   INVASION OF ERYTHROCYTES BY MALARIA MEROZOITES [J].
DVORAK, JA ;
MILLER, LH ;
WHITEHOUSE, WC ;
SHIROISHI, T .
SCIENCE, 1975, 187 (4178) :748-750
[9]   Lipid microdomains in cell surface membranes [J].
Edidin, M .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1997, 7 (04) :528-532
[10]   Shrinking patches and slippery rafts: scales of domains in the plasma membrane [J].
Edidin, M .
TRENDS IN CELL BIOLOGY, 2001, 11 (12) :492-496