Yilmaz Neval, Kobayashi Toshihide
Lipid Biology Laboratory, RIKEN, Wako, Saitama 351-0198, Japan.
Lipid Biology Laboratory, RIKEN, Wako, Saitama 351-0198, Japan; INSERM U106-Université Lyon1, 69621 Villeurbanne, France.
Biochim Biophys Acta. 2016 Mar;1858(3):500-11. doi: 10.1016/j.bbamem.2015.11.005. Epub 2015 Nov 12.
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.
许多成孔毒素(PFTs)能够通过与脂质的特异性相互作用在脂质膜上组装。一些PFTs的寡聚体组装已通过电子显微镜(EM)和/或原子力显微镜(AFM)成功揭示。与EM不同,AFM成像可在生理条件下进行,能够实时观察PFT组装以及从毒素不跨越膜的前孔状态到孔状态的转变。除了表征PFT寡聚体外,AFM还被用于研究毒素诱导的膜组织变化。在本综述中,我们总结了AFM在理解PFT组装和PFT诱导的膜重组方面所做的贡献。本文是由Mauro Dalla Serra和Franco Gambale编辑的名为《成孔毒素》的特刊的一部分。