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How membrane lipids control the 3D structure and function of receptors
被引:5
作者:
Fantini, Jacques
[1
]
Barrantes, Francisco J.
[2
]
机构:
[1] Aix Marseille Univ, INSERM, UMR 1072, Blvd Pierre Dramard, F-13015 Marseille, France
[2] Consejo Nacl Invest Cient & Tecn, UCA, Inst Biomed Res BIOMED, Lab Mol Neurobiol, Buenos Aires, DF, Argentina
关键词:
cholesterol;
sphingolipids;
hopanoids;
lipid rafts;
ion channels;
GPCR;
D O I:
10.3934/biophy.2018.1.22
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
The cohabitation of lipids and proteins in the plasma membrane of mammalian cells is controlled by specific biochemical and biophysical rules. Lipids may be either constitutively tightly bound to cell-surface receptors (non-annular lipids) or less tightly attached to the external surface of the protein (annular lipids). The latter are exchangeable with surrounding bulk membrane lipids on a faster time scale than that of non-annular lipids. Not only do non-annular lipids bind to membrane proteins through stereoselective mechanisms, they can also help membrane receptors acquire (or maintain) a functional 3D structure. Cholesterol is the prototype of membrane lipids that finely controls the 3D structure and function of receptors. However, several other lipids such as sphingolipids may also modulate the function of membrane proteins though conformational adjustments. All these concepts are discussed in this review in the light of representative examples taken from the literature.
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页码:22 / 35
页数:14
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