Structural determinants of protein partitioning into ordered membrane domains and lipid rafts

被引:120
|
作者
Lorent, Joseph Helmuth [1 ]
Levental, Ilya [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Integrat Biol & Pharmacol, Houston, TX 77030 USA
关键词
Lipid rafts; Partitioning; Membrane order; Liquid ordered; Membrane domains; INFLUENZA-VIRUS HEMAGGLUTININ; GPI-ANCHORED PROTEINS; PLACENTAL ALKALINE-PHOSPHATASE; DETERGENT-RESISTANT MEMBRANES; SINGLE-MOLECULE TRACKING; PLASMA-MEMBRANE; TRANSMEMBRANE DOMAIN; MODEL MEMBRANES; CHAIN-LENGTH; BILAYER THICKNESS;
D O I
10.1016/j.chemphyslip.2015.07.022
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
Increasing evidence supports the existence of lateral nanoscopic lipid domains in plasma membranes, known as lipid rafts. These domains preferentially recruit membrane proteins and lipids to facilitate their interactions and thereby regulate transmembrane signaling and cellular homeostasis. The functionality of raft domains is intrinsically dependent on their selectivity for specific membrane components; however, while the physicochemical determinants of raft association for lipids are known, very few systematic studies have focused on the structural aspects that guide raft partitioning of proteins. In this review, we describe biophysical and thermodynamic aspects of raft-mimetic liquid ordered phases, focusing on those most relevant for protein partitioning. Further, we detail the variety of experimental models used to study protein-raft interactions. Finally, we review the existing literature on mechanisms for raft targeting, including lipid post-translational modifications, lipid binding, and transmembrane domain features. We conclude that while protein palmitoylation is a clear raft-targeting signal, few other general structural determinants for raft partitioning have been revealed, suggesting that many discoveries lie ahead in this burgeoning field. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:23 / 32
页数:10
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