Lipid domains in the exoplasmic and cytoplasmic leaflet of the human erythrocyte membrane:: a spin label approach

被引:18
作者
Zuvic-Butorac, M
Müller, P
Pomorski, T
Libera, J
Herrmann, A
Schara, M
机构
[1] Humboldt Univ, Fak Math Nat 1, Inst Biol Biophys, D-10115 Berlin, Germany
[2] Univ Rijeka, Rijeka, Croatia
[3] Univ Ljubljana, Jozef Stefan Inst, SI-1000 Ljubljana, Slovenia
来源
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS | 1999年 / 28卷 / 04期
关键词
erythrocyte; plasma membrane; leaflet; lipid domains; spin label;
D O I
10.1007/s002490050212
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The existence of different lipid domains in the monolayers of the human erythrocyte membrane was investigated at 4 degrees C by employing spin-labelled phospholipid analogues. Spectra of analogues located exclusively either in the exoplasmic or in the cytoplasmic leaflet of erythrocyte membranes were recorded. Spectra were simulated by variation of order parameter describing the average amplitude of motion of the long molecular axis of the nitrogen 2p pi orbital of the spin label and of the respective correlation times. For both leaflets at least three components were required to fit the experimental spectra, differing mainly in the order parameter. While the parameters of each component are not very different between both membrane halves, the relative contribution of each component to the spectrum is different between the exoplasmic and cytoplasmic leaflet. The order parameter of the most fluid component, presumably resembling the lipid bulk phase, is smaller in the cytoplasmic leaflet in comparison to the exoplasmic one. The lateral coexistence of different lipid domains in the human red blood cell membrane is concluded. The molecular nature of those domains is discussed.
引用
收藏
页码:302 / 311
页数:10
相关论文
共 37 条
[1]   On the origin of sphingolipid/cholesterol-rich detergent-insoluble cell membranes: Physiological concentrations of cholesterol and sphingolipid induce formation of a detergent-insoluble, liquid-ordered lipid phase in model membranes [J].
Ahmed, SN ;
Brown, DA ;
London, E .
BIOCHEMISTRY, 1997, 36 (36) :10944-10953
[2]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[3]   LIPID INTERMOLECULAR HYDROGEN-BONDING - INFLUENCE ON STRUCTURAL ORGANIZATION AND MEMBRANE-FUNCTION [J].
BOGGS, JM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 906 (03) :353-404
[4]   INTERMOLECULAR HYDROGEN-BONDING BETWEEN LIPIDS - INFLUENCE ON ORGANIZATION AND FUNCTION OF LIPIDS IN MEMBRANES [J].
BOGGS, JM .
CANADIAN JOURNAL OF BIOCHEMISTRY, 1980, 58 (10) :755-770
[5]   Structure and origin of ordered lipid domains in biological membranes [J].
Brown, DA ;
London, E .
JOURNAL OF MEMBRANE BIOLOGY, 1998, 164 (02) :103-114
[6]   ASYMMETRIC DISTRIBUTION OF PHOSPHOLIPIDS IN SPECTRIN-POOR ERYTHROCYTE VESICLES [J].
CALVEZ, JY ;
ZACHOWSKI, A ;
HERRMANN, A ;
MORROT, G ;
DEVAUX, PF .
BIOCHEMISTRY, 1988, 27 (15) :5666-5670
[7]  
CRIBIER S, 1990, EUR BIOPHYS J, V18, P33, DOI 10.1007/BF00185418
[8]   SPECIFICITY OF LIPID-PROTEIN INTERACTIONS AS DETERMINED BY SPECTROSCOPIC TECHNIQUES [J].
DEVAUX, PF ;
SEIGNEURET, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 822 (01) :63-125
[9]   STATIC AND DYNAMIC LIPID ASYMMETRY IN CELL-MEMBRANES [J].
DEVAUX, PF .
BIOCHEMISTRY, 1991, 30 (05) :1163-1173
[10]   Interactions of the nicotinic acetylcholine receptor transmembrane segments with the lipid bilayer in native receptor-rich membranes [J].
Dreger, M ;
Krauss, M ;
Herrmann, A ;
Hucho, F .
BIOCHEMISTRY, 1997, 36 (04) :839-847