Janshoff A, Steinem C
Institut für Physikalische Chemie, Johannes-Gutenberg-Universität, Jakob-Welder-Weg 11, 55128 Mainz, Germany.
Chembiochem. 2001 Nov 5;2(11):798-808. doi: 10.1002/1439-7633(20011105)2:11<798::AID-CBIC798>3.0.CO;2-L.
Visualization of biological membranes by scanning force microscopy (SFM) has tremendously improved the current understanding of protein-lipid interactions under physiological conditions. SFM is the only tool to directly image processes on surfaces in aqueous solution at molecular resolution. Besides being a supportive means to confirm results on lipid phases and domains obtained from fluorescence spectroscopy, calorimetry, and X-ray crystallography, SFM has contributed distinct aspects on the formation of 2D crystals of various membrane-confined proteins and morphological changes of membranes due to the interaction of peptides and proteins. This review will focus on recent results in SFM imaging of artificial solid-supported membranes, their phase behavior as a response to the environment, and changes in membrane morphology induced by the partitioning of peptides and proteins.
通过扫描力显微镜(SFM)对生物膜进行可视化,极大地增进了我们目前对生理条件下蛋白质 - 脂质相互作用的理解。SFM是唯一能够在分子分辨率下直接对水溶液表面过程进行成像的工具。除了作为一种辅助手段来确认从荧光光谱、量热法和X射线晶体学获得的关于脂质相和结构域的结果外,SFM在各种膜结合蛋白二维晶体的形成以及由于肽和蛋白质相互作用导致的膜形态变化方面也有独特贡献。本综述将聚焦于人工固体支撑膜的SFM成像的最新结果、它们对环境响应的相行为以及由肽和蛋白质分配引起的膜形态变化。