Single-molecule fluorescence vistas of how lipids regulate membrane proteins

被引:3
|
作者
Ward, Alyssa E. [1 ]
Ye, Yujie [1 ]
Schuster, Jennifer A. [1 ]
Wei, Shushu [1 ]
Barrera, Francisco N. [1 ]
机构
[1] Univ Tennessee, Dept Biochem & Cellular & Mol Biol, Knoxville, TN 37996 USA
基金
美国国家卫生研究院;
关键词
BILAYER THICKNESS; POTASSIUM-CHANNEL; EPHA2; CHOLESTEROL; DIMERIZATION; STABILITY; DOMAINS; CURVATURE; DIVERSITY; INTERPLAY;
D O I
10.1042/BST20201074
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 study of membrane proteins is undergoing a golden era, and we are gaining unprecedented knowledge on how this key group of proteins works. However, we still have only a basic understanding of how the chemical composition and the physical properties of lipid bilayers control the activity of membrane proteins. Single-molecule (SM) fluorescence methods can resolve sample heterogeneity, allowing to discriminate between the different molecular populations that biological systems often adopt. This short review highlights relevant examples of how SM fluorescence methodologies can illuminate the different ways in which lipids regulate the activity of membrane proteins. These studies are not limited to lipid molecules acting as ligands, but also consider how the physical properties of the bilayer can be determining factors on how membrane proteins function.
引用
收藏
页码:1685 / 1694
页数:10
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