Fluorescence energy transfer reveals microdomain formation at physiological temperatures in lipid mixtures modeling the outer leaflet of the plasma membrane

被引:125
作者
Silvius, JR [1 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
关键词
D O I
10.1016/S0006-3495(03)74542-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An approach is described using fluorescence resonance energy transfer (FRET) to detect inhomogeneity in lipid organization, on distance scales of the order of tens of nanometers or greater, in lipid bilayers. This approach compares the efficiency of energy transfer between two matched fluorescent lipid donors, differing in their affinities for ordered versus disordered regions of the bilayer, and an acceptor lipid that distributes preferentially into disordered regions. Inhomogeneities in bilayer organization, on spatial scales of tens of nanometers or greater, are detected as a marked difference in the efficiencies of quenching of fluorescence of the two donor species by the acceptor. Using a novel pair of 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD)-labeled tetraacyl lipids as donor species with a rhodaminyl-labeled acceptor, this strategy faithfully reports homo-versus inhomogeneous mixing in each of several lipid bilayer systems whose organization on the FRET distance scale can be predicted from previous findings. Interestingly, however, the present FRET method reports clear evidence of inhomogeneity in the organization of mixtures combining sphingomyelin or saturated phospholipids with unsaturated phospholipids and physiological proportions of cholesterol, even at physiological temperatures where these systems have been reported to appear homogeneous by fluorescence microscopy. These results indicate that under physiological conditions, lipid mixtures mimicking the lipid composition of the outer lea. et of the plasma membrane can form domains on a spatial scale comparable to that inferred for the dimensions of lipid rafts in biological membranes.
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页码:1034 / 1045
页数:12
相关论文
共 64 条
[41]   Critical role for cholesterol in Lyn-mediated tyrosine phosphorylation of FcεRI and their association with detergent-resistant membranes [J].
Sheets, ED ;
Holowka, D ;
Baird, B .
JOURNAL OF CELL BIOLOGY, 1999, 145 (04) :877-887
[42]   CHOLESTEROL MODULATION OF LIPID INTERMIXING IN PHOSPHOLIPID AND GLYCOSPHINGOLIPID MIXTURES - EVALUATION USING FLUORESCENT LIPID PROBES AND BROMINATED LIPID QUENCHERS [J].
SILVIUS, JR .
BIOCHEMISTRY, 1992, 31 (13) :3398-3408
[43]   Cholesterol at different bilayer concentrations can promote or antagonize lateral segregation of phospholipids of differing acyl chain length [J].
Silvius, JR ;
delGiudice, D ;
Lafleur, M .
BIOCHEMISTRY, 1996, 35 (48) :15198-15208
[44]   Lipid rafts and signal transduction [J].
Simons, K ;
Toomre, D .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) :31-39
[45]   Functional rafts in cell membranes [J].
Simons, K ;
Ikonen, E .
NATURE, 1997, 387 (6633) :569-572
[46]  
Smart EJ, 2002, METHOD ENZYMOL, V353, P131
[47]   PARTITIONING BEHAVIOR OF INDOCARBOCYANINE PROBES BETWEEN COEXISTING GEL AND FLUID PHASES IN MODEL MEMBRANES [J].
SPINK, CH ;
YEAGER, MD ;
FEIGENSON, GW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1023 (01) :25-33
[48]   Detection of lipid domains in docosahexaenoic acid-rich bilayers by acyl chain-specific FRET probes [J].
Stillwell, W ;
Jenski, LJ ;
Zerouga, M ;
Dumaual, AF .
CHEMISTRY AND PHYSICS OF LIPIDS, 2000, 104 (02) :113-132
[49]   USE OF RESONANCE ENERGY-TRANSFER TO MONITOR MEMBRANE-FUSION [J].
STRUCK, DK ;
HOEKSTRA, D ;
PAGANO, RE .
BIOCHEMISTRY, 1981, 20 (14) :4093-4099
[50]   RETRACTED: Cholesterol detection inhibits epidermal growth factor receptor transactivation by angiotensin II in vascular smooth muscle cells - Role of cholesterol-rich microdomains and focal adhesions in angiotensin II signaling (Retracted Article) [J].
Ushio-Fukai, M ;
Hilenski, L ;
Santanam, N ;
Becker, PL ;
Ma, YX ;
Griendling, KK ;
Alexander, RW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :48269-48275