Structure and mechanics of membrane proteins

被引:188
作者
Engel, Andreas [1 ]
Gaub, Hermann E. [2 ,3 ]
机构
[1] Univ Basel, Biozentrum, Maurice E Muller Inst Struct Biol, CH-4056 Basel, Switzerland
[2] Univ Munich, Ctr Neurosci, D-80799 Munich, Germany
[3] Univ Munich, Dept Phys, D-80799 Munich, Germany
关键词
atomic force microscope; bacteriorhodopsin; folding potential; ligand binding; scanning electrochemical microscope; single-molecule force spectroscopy;
D O I
10.1146/annurev.biochem.77.062706.154450
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
Evolution has tuned membrane proteins to exist in a lipid bilayer, provide for cell-cell communication, transport solutes, and convert energies. These proteins exhibit a hydrophobic belt that interacts with the lipid bilayer. Detergents are therefore used to extract membrane proteins and keep them in solution for purification and subsequent analyses. However, most membrane proteins are unstable when solubilized and hence often not accessible to NMR or X-ray crystallography. The atomic force microscope (AFM) is a powerful tool for imaging and manipulating membrane proteins in their native state. Superb images of native membranes have been recorded, and a quantitative interpretation of the data acquired using the AFM tip has become possible. In addition, multifunctional probes to simultaneously acquire information on the topography and electrical properties of membrane proteins have been produced. This progress is discussed here and fosters expectations for future developments and applications of AFM and single-molecule force spectroscopy.
引用
收藏
页码:127 / 148
页数:22
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