Structure and function of membrane rafts

被引:0
作者
Brown, D [1 ]
机构
[1] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
关键词
raft; cholesterol; sphingolipid; GPI-anchored protein; liquid-ordered;
D O I
暂无
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lipids do not always mix uniformly in membranes, but can cluster to form microdomains. We will consider one type of microdomain that can form in cell membranes. These are enriched in cholesterol and sphingolipids, and are referred to as rafts. Rafts probably exist in membranes in the liquid-ordered phase or a phase with similar properties. We will briefly review membrane lipid phase behavior, and the differences between liquid-crystalline, liquid-ordered, and gel-phase membrane bilayer domains. We will present evidence suggesting that phospholipid-rich, liquid-crystalline phase domains and sphingolipid-rich, liquid-ordered phase domains (rafts) can exist in equilibrium in biological membranes, especially the plasma membrane. Preferential partitioning of membrane proteins into rafts can affect function. Among the proteins that are targeted to rafts are those anchored in the outer leaflet of the membrane through covalent attachment to a special glycolipid, glycosyl phosphatidylinositol (GPI). Other proteins that are linked to saturated acyl chains, such as those that are directly acylated with two or more palmitate chains, or a palmitate and a myristate chain, are also targeted to rafts. Targeting of GPI-anchored proteins and other proteins to rafts plays a role in signal transduction in hematopoietic cells, and possibly also in sorting in intracellular membranes and regulation of cell-surface proteolysis in other mammalian cells.
引用
收藏
页码:433 / 437
页数:5
相关论文
共 29 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]   SORTING AND INTRACELLULAR TRAFFICKING OF A GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED PROTEIN AND 2 HYBRID TRANSMEMBRANE PROTEINS WITH THE SAME ECTODOMAIN IN MADIN-DARBY CANINE KIDNEY EPITHELIAL-CELLS [J].
ARREAZA, G ;
BROWN, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23641-23647
[3]   Functions of lipid rafts in biological membranes [J].
Brown, DA ;
London, E .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :111-136
[4]   MECHANISM OF MEMBRANE ANCHORING AFFECTS POLARIZED EXPRESSION OF 2 PROTEINS IN MDCK CELLS [J].
BROWN, DA ;
CRISE, B ;
ROSE, JK .
SCIENCE, 1989, 245 (4925) :1499-1501
[5]   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
[6]   Structure and origin of ordered lipid domains in biological membranes [J].
Brown, DA ;
London, E .
JOURNAL OF MEMBRANE BIOLOGY, 1998, 164 (02) :103-114
[7]   AN AUTONOMOUS SIGNAL FOR BASOLATERAL SORTING IN THE CYTOPLASMIC DOMAIN OF THE POLYMERIC IMMUNOGLOBULIN RECEPTOR [J].
CASANOVA, JE ;
APODACA, G ;
MOSTOV, KE .
CELL, 1991, 66 (01) :65-75
[8]  
CINEK T, 1992, J IMMUNOL, V149, P2262
[9]   THE ROLE OF N-GLYCANS IN THE SECRETORY PATHWAY [J].
FIEDLER, K ;
SIMONS, K .
CELL, 1995, 81 (03) :309-312
[10]   Electron spin resonance characterization of liquid ordered phase of detergent-resistant membranes from RBL-2H3 cells [J].
Ge, MT ;
Field, KA ;
Aneja, R ;
Holowka, D ;
Baird, B ;
Freed, JH .
BIOPHYSICAL JOURNAL, 1999, 77 (02) :925-933