Lipid-protein interactions in GPCR-associated signaling

被引:138
作者
Escriba, Pablo V.
Wedegaertner, Philip B.
Goni, Felix M.
Vogler, Oliver
机构
[1] Univ Balearic Isl, Dept Biol, IUNICS, Lab Mol & Cellular Biomed, E-07122 Palma de Mallorca, Spain
[2] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
[3] Univ Basque Country, Dept Bioquim, E-48080 Bilbao, Spain
[4] Univ Balearic Isl, EHU, CSIC, Ctr Mixto,Unidad Biofis, E-07122 Palma de Mallorca, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2007年 / 1768卷 / 04期
关键词
signal transduction; membrane structure; G-protein-coupled receptor; G protein; palmitoylation; myristoylation; isoprenylation; farnesyl; geranylgeraniol; phospholipase C; protein kinase C;
D O I
10.1016/j.bbamem.2006.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Signal transduction via G-protein-coupled receptors (GPCRs) is a fundamental pathway through which the functions of an individual cell can be integrated within the demands of a multicellular organism. Since this family of receptors first discovered, the proteins that constitute this signaling cascade and their interactions with one another have been studied intensely. In parallel, the pivotal role of lipids in the correct and efficient propagation of extracellular signals has attracted ever increasing attention. This is not surprising given that most of the signal transduction machinery is membrane-associated and therefore lipid-related. Hence, lipid-protein interactions exert a considerable influence on the activity of these proteins. This review focuses on the post-translational lipid modifications of GPCRs and G proteins (palmitoylation, myristoylation, and isoprenylation) and their significance for membrane binding, trafficking and signaling. Moreover, we address how the particular biophysical properties of different membrane structures may regulate the localization of these proteins and the potential functional consequences of this phenomenon in signal transduction. Finally, the interactions that occur between membrane lipids and GPCR effector enzymes such as PLC and PKC are also considered. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:836 / 852
页数:17
相关论文
共 210 条
[1]  
ADAMSON P, 1992, J BIOL CHEM, V267, P20033
[2]   Modulation of PI-specific phospholipase C by membrane curvature and molecular order [J].
Ahyayauch, H ;
Villar, AV ;
Alonso, A ;
Goñi, FM .
BIOCHEMISTRY, 2005, 44 (34) :11592-11600
[3]   β-adrenergic receptor stimulation promotes Gαs internalization through lipid rafts:: A study in living cells [J].
Allen, JA ;
Yu, JZ ;
Donati, RJ ;
Rasenick, MM .
MOLECULAR PHARMACOLOGY, 2005, 67 (05) :1493-1504
[4]  
Alves ID, 2005, BIOPHYS J, V88, P198, DOI [10.1529/biophysj.104.046722, 10.1529/biophj.104.046722]
[5]   X-ray structure of the R69D phosphatidylinositol-specific phospholipase C enzyme: Insight into the role of calcium and surrounding amino acids in active site geometry and catalysis [J].
Apiyo, D ;
Zhao, L ;
Tsai, MD ;
Selby, TL .
BIOCHEMISTRY, 2005, 44 (30) :9980-9989
[6]   Cholesterol dynamics in membranes of raft composition:: A molecular point of view from 2H and 31P solid-state NMR [J].
Aussenac, F ;
Tavares, M ;
Dufourc, EJ .
BIOCHEMISTRY, 2003, 42 (06) :1383-1390
[7]  
BARD F, 2006, IN PRESS ANN REV CEL
[8]   Effect of olive oil on early and late events of colon carcinogenesis in rats:: modulation of arachidonic acid metabolism and local prostaglandin E2 synthesis [J].
Bartoli, R ;
Fernández-Bañares, F ;
Navarro, E ;
Castellà, E ;
Mañé, J ;
Alvarez, M ;
Pastor, C ;
Cabré, E ;
Gassull, MA .
GUT, 2000, 46 (02) :191-199
[9]   Origin of the lag period in the phospholipase C cleavage of phospholipids in membranes. Concomitant vesicle aggregation and enzyme activation [J].
Basanez, G ;
Nieva, JL ;
Goni, FM ;
Alonso, A .
BIOCHEMISTRY, 1996, 35 (48) :15183-15187
[10]  
BELL RM, 1991, J BIOL CHEM, V266, P4661