Transfer on hydrophobic substrates and AFM imaging of membrane proteins reconstituted in planar lipid bilayers

被引:3
|
作者
Seantier, Bastien [2 ]
Dezi, Manuela [1 ]
Gubellini, Francesca [1 ]
Berquand, Alexandre [1 ]
Godefroy, Cedric [2 ]
Dosset, Patrice [2 ]
Levy, Daniel [1 ]
Milhiet, Pierre-Emmanuel [2 ]
机构
[1] Inst Curie, UMR CNRS 168, F-75248 Paris 05, France
[2] UM2, Ctr Biochim Struct, INSERM, UMR 5048,U554,UM1,CNRS, Montpellier, France
关键词
atomic force microscopy; membrane protein; structure; 2D crystallization; Shiga toxin; ABC transporter; 2-DIMENSIONAL CRYSTALLIZATION; ELECTRON CRYSTALLOGRAPHY; TRANSPORTER BMRA; 2D CRYSTALS; RESOLUTION; LAYER;
D O I
10.1002/jmr.1070
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 lipid-layer technique allows reconstituting transmembrane proteins at a high density in microns size planar membranes and suspended to a lipid monolayer at the air/water interface. In this paper, we transferred these membranes onto two hydrophobic substrates for further structural analysis of reconstituted proteins by Atomic Force Microscopy (AFM). We used a mica sheet covered by a lipid monolayer or a sheet of highly oriented pyrolytic graphite (HOPG) to trap the lipid monolayer at the interface and the suspended membranes. In both cases, we succeeded in the transfer of large membrane patches containing densely packed or 2D-crystallized proteins. As a proof of concept, we transferred and imaged the soluble Shiga toxin bound to its lipid ligand and the ATP-binding cassette (ABC) transporter BmrA reconstituted into a planar bilayer. AFM imaging with a lateral resolution in the nanometer range was achieved. Potential applications of this technique in structural biology and nanobiotechnology are discussed. Copyright (C) 2011 John Wiley & Sons, Ltd.
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页码:461 / 466
页数:6
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