Dufrêne Yves F
Université Catholique de Louvain, Unité de chimie des interfaces/Nanobio team, Croix du Sud 2/18, Louvain-la-Neuve, Belgium.
Future Microbiol. 2006 Dec;1(4):387-96. doi: 10.2217/17460913.1.4.387.
Atomic force microscopy (AFM) has recently opened a variety of novel possibilities for imaging and manipulating microbial surfaces in their native environment. While AFM imaging offers a means to visualize surface structures at high resolution and in physiological conditions, AFM force spectroscopy enables researchers to probe a variety of properties, including the unfolding pathways of single-membrane proteins, the elasticity of cell walls and surface macromolecules, and the molecular forces responsible for cell-cell and cell-solid interactions. These nanoscale analyses enable us to answer a number of questions that were difficult to address previously, such as: how does the surface architecture of microbes change as they grow or interact with antibiotics; what is the force required to unfold and extract a single membrane protein; and what are the molecular forces driving the interaction between a pathogen and a host or biomaterial surface? This review will expand on these issues.
原子力显微镜(AFM)最近为在原生环境中成像和操纵微生物表面开辟了各种新的可能性。虽然AFM成像提供了一种在生理条件下以高分辨率可视化表面结构的方法,但AFM力谱使研究人员能够探测各种特性,包括单膜蛋白的展开途径、细胞壁和表面大分子的弹性以及负责细胞间和细胞与固体相互作用的分子力。这些纳米级分析使我们能够回答一些以前难以解决的问题,例如:微生物的表面结构在其生长或与抗生素相互作用时如何变化;展开和提取单个膜蛋白所需的力是多少;以及驱动病原体与宿主或生物材料表面相互作用的分子力是什么?本综述将详细阐述这些问题。