Model membrane platforms to study protein-membrane interactions

被引:62
|
作者
Sezgin, Erdinc [1 ,2 ]
Schwille, Petra [1 ,3 ]
机构
[1] Tech Univ Dresden, Biophys BIOTEC, D-01307 Dresden, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, Dresden, Germany
[3] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
Membrane model; membrane lipid; membrane protein; GIANT UNILAMELLAR VESICLES; 2-PHOTON FLUORESCENCE MICROSCOPY; LATERAL PRESSURE PROFILE; LIPID-BILAYERS; PHOSPHOLIPID-COMPOSITION; MEDIATED INTERACTIONS; ALKALINE-PHOSPHATASE; AMPHIPATHIC HELICES; SYNTHETIC BIOLOGY; ANCHORED PROTEINS;
D O I
10.3109/09687688.2012.700490
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
Constituting functional interactions between proteins and lipid membranes is one of the essential features of cellular membranes. The major challenge of quantitatively studying these interactions in living cells is the multitude of involved components that are difficult, if not impossible, to simultaneously control. Therefore, there is great need for simplified but still sufficiently detailed model systems to investigate the key constituents of biological processes. To specifically focus on interactions between membrane proteins and lipids, several membrane models have been introduced which recapitulate to varying degrees the complexity and physicochemical nature of biological membranes. Here, we summarize the presently most widely used minimal model membrane systems, namely Supported Lipid Bilayers (SLBs), Giant Unilamellar Vesicles (GUVs) and Giant Plasma Membrane Vesicles (GPMVs) and their applications for protein-membrane interactions.
引用
收藏
页码:144 / 154
页数:11
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