Insights from biophysical studies on the role of polyunsaturated fatty acids for function of G-protein coupled membrane receptors

被引:55
作者
Gawrisch, Klaus [1 ]
Soubias, Olivier [1 ]
Mihailescu, Mihaela [2 ]
机构
[1] NIAAA, Sect NMR, Lab Membrane Biochem & Biophys, NIH, Bethesda, MD 20892 USA
[2] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92717 USA
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2008年 / 79卷 / 3-5期
关键词
Docosahexaenoic acid; G-protein-coupled membrane receptor; Rhodopsin; Nuclear Magnetic Resonance; Neutron Scattering;
D O I
10.1016/j.plefa.2008.09.002
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
The composition of the lipid matrix is critical for function of membrane proteins. Perhaps one of the best studied examples is the function of the G-protein-coupled membrane receptor (GPCR) rhodopsin which is located in membranes with high content of phospholipids with polyunsaturated docosahexaenoic acid chains (DHA, 22:6n-3). Technological advances enabled a more detailed study of structure and dynamics of DHA chains and their interaction with rhodopsin. It was established that polyunsaturated DHA differs from saturated and monounsaturated hydrocarbon chains by far more rapid structural conversions. Furthermore, DHA chains tend to have higher density near the lipid/water inter-face while density of saturated chains is higher in the bilayer center. The interface of rhodopsin has a small number of sites for tighter interaction with DHA. Polyunsaturated phosphatidylethanolamines accumulate preferentially near the protein. Surprisingly, the high conformational freedom of most DHA chains is not measurably reduced upon interaction with rhodopsin. While some observations point at an involvement of continuum elastic properties of membranes in modulation of rhodopsin function, there is growing evidence for a role of weakly specific DHA-rhodopsin interactions. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:131 / 134
页数:4
相关论文
共 39 条
[1]  
APPLEGATE KR, 1991, J LIPID RES, V32, P1635
[2]  
APPLEGATE KR, 1986, J LIPID RES, V27, P658
[3]  
Balendiran GK, 2000, J BIOL CHEM, V275, P27045
[4]   Dehydration induces lateral expansion of polyunsaturated 18:0-22:6 phosphatidylcholine in a new lamellar phase [J].
Binder, H ;
Gawrisch, K .
BIOPHYSICAL JOURNAL, 2001, 81 (02) :969-982
[5]   Effect of unsaturated lipid chains on dimensions, molecular order and hydration of membranes [J].
Binder, H ;
Gawrisch, K .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (49) :12378-12390
[6]   Conformational energetics of rhodopsin modulated by nonlamellar-forming lipids [J].
Botelho, AV ;
Gibson, NJ ;
Thurmond, RL ;
Wang, Y ;
Brown, MF .
BIOCHEMISTRY, 2002, 41 (20) :6354-6368
[7]   Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling [J].
Bracey, MH ;
Hanson, MA ;
Masuda, KR ;
Stevens, RC ;
Cravatt, BF .
SCIENCE, 2002, 298 (5599) :1793-1796
[8]   Lipid composition and the lateral pressure profile in bilayers [J].
Cantor, RS .
BIOPHYSICAL JOURNAL, 1999, 76 (05) :2625-2639
[9]   Lateral pressures in cell membranes: A mechanism for modulation of protein function [J].
Cantor, RS .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (10) :1723-1725
[10]   Evidence for a mechanism by which ω-3 polyunsaturated lipids may affect membrane protein function [J].
Carrillo-Tripp, M ;
Feller, SE .
BIOCHEMISTRY, 2005, 44 (30) :10164-10169