Assemblies of pore-forming toxins visualized by atomic force microscopy

被引:22
作者
Yilmaz, Neval [1 ]
Kobayashi, Toshihide [1 ,2 ]
机构
[1] RIKEN, Lipid Biol Lab, Wako, Saitama 3510198, Japan
[2] Univ Lyon 1, INSERM, U106, F-69621 Villeurbanne, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2016年 / 1858卷 / 03期
关键词
Oligomer; Supported lipid bilayer; Phase boundary; High resolution; Real time; AFM imaging; STAPHYLOCOCCAL ALPHA-HEMOLYSIN; SUPPORTED LIPID-BILAYERS; CHOLESTEROL-DEPENDENT CYTOLYSIN; TRANSMEMBRANE BETA-HAIRPINS; SCANNING PROBE MICROSCOPY; RESOLUTION AFM TOPOGRAPHS; NATIVE MEMBRANE-PROTEINS; PHOSPHOLIPID-BILAYERS; IN-SITU; SUBNANOMETER RESOLUTION;
D O I
10.1016/j.bbamem.2015.11.005
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
A number of pore-forming toxins (PFTs) can assemble on lipid membranes through their specific interactions with lipids. The oligomeric assemblies of some PFTs have been successfully revealed either by electron microscopy (EM) and/or atomic force microscopy (AFM). Unlike EM, AFM imaging can be performed under physiological conditions, enabling the real-time visualization of PFT assembly and the transition from the prepore state, in which the toxin does not span the membrane, to the pore state. In addition to characterizing PFT oligomers, AFM has also been used to examine toxin-induced alterations in membrane organization. In this review, we summarize the contributions of AFM to the understanding of both PFT assembly and PFT-induced membrane reorganization. This article is part of a Special Issue entitled: Pore-Forming Toxins edited by Mauro Dalla Serra and Franco Gambale. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:500 / 511
页数:12
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