Distribution of ganglioside GM1 in L-α-dipalmitoylphosphatidylcholine/cholesterol monolayers:: A model for lipid rafts

被引:107
作者
Yuan, CB [1 ]
Johnston, LJ [1 ]
机构
[1] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
关键词
D O I
10.1016/S0006-3495(00)76516-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The distribution of low concentrations of ganglioside GM1 in L-alpha -dipalmitoylphosphatidylcholine (DPPC) and DPPC/cholesterol monolayers supported on mica has been studied using atomic force microscopy (AFM). The monolayers studied correspond to a pure gel phase and a mixture of liquid-expanded (LE) and liquid-condensed (LC) phases for DPPC and to a single homogeneous liquid-ordered phase for 2:1 DPPC/cholesterol. The addition of 2.56% GM1 to phase-separated DPPC monolayers resulted in small round ganglioside-rich microdomains in the center and at the edges of the LC domains. Higher amounts of GM1 (10%) give numerous filaments in the center of the LC domains and larger patches at the edges. A gel phase DPPC monolayer containing GM1 showed large domains containing a network of GM1-rich filaments. The addition of GM1 to a liquid-ordered 2:1 DPPC/cholesterol monolayer gives small, round domains that vary in size from 50 to 150 nm for a range of surface pressures. Larger amounts of GM1 lead to coalescence of the small, round domains to give longer filaments that cover 30-40% of the monolayer surface for 10 mol % GM1. The results indicate that biologically relevant GM1 concentrations lead to submicron-sized domains in a cholesterol-rich liquid-ordered phase that is analogous to that found in detergent-insoluble membrane fractions, and are thought to be important in membrane microdomains or rafts. This demonstrates that AFM studies of model monolayers and bilayers provide a powerful method for the direct detection of microdomains that are too small for study with most other techniques.
引用
收藏
页码:2768 / 2781
页数:14
相关论文
共 49 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]   CALORIMETRIC STUDIES ON VARIOUS GANGLIOSIDES AND GANGLIOSIDE-LIPID INTERACTIONS [J].
BACH, D ;
MILLER, IR ;
SELA, BA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 686 (02) :233-239
[3]   Two photon fluorescence microscopy of coexisting lipid domains in giant unilamellar vesicles of binary phospholipid mixtures [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :290-305
[4]   SURFACE DIPOLE DENSITIES IN LIPID MONOLAYERS [J].
BENVEGNU, DJ ;
MCCONNELL, HM .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (25) :6686-6691
[5]   Functions of lipid rafts in biological membranes [J].
Brown, DA ;
London, E .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :111-136
[6]   SORTING OF GPI-ANCHORED PROTEINS TO GLYCOLIPID-ENRICHED MEMBRANE SUBDOMAINS DURING TRANSPORT TO THE APICAL CELL-SURFACE [J].
BROWN, DA ;
ROSE, JK .
CELL, 1992, 68 (03) :533-544
[7]   Structure and origin of ordered lipid domains in biological membranes [J].
Brown, DA ;
London, E .
JOURNAL OF MEMBRANE BIOLOGY, 1998, 164 (02) :103-114
[8]   DOMAIN-STRUCTURES IN LANGMUIR-BLODGETT-FILMS INVESTIGATED BY ATOMIC FORCE MICROSCOPY [J].
CHI, LF ;
ANDERS, M ;
FUCHS, H ;
JOHNSTON, RR ;
RINGSDORF, H .
SCIENCE, 1993, 259 (5092) :213-216
[9]   CLUSTERING OF GANGLIOSIDES IN PHOSPHOLIPID-BILAYERS [J].
DELMELLE, M ;
DUFRANE, SP ;
BRASSEUR, R ;
RUYSSCHAERT, JM .
FEBS LETTERS, 1980, 121 (01) :11-14
[10]   RELATION BETWEEN VARIOUS PHOSPHOLIPASE ACTIONS ON HUMAN RED-CELL MEMBRANES AND INTERFACIAL PHOSPHOLIPID PRESSURE IN MONOLAYERS [J].
DEMEL, RA ;
GEURTSVANKESSEL, WSM ;
ZWAAL, RFA ;
ROELOFSEN, B ;
VANDEENEN, LLM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 406 (01) :97-107