Shao Z, Yang J, Somlyo A P
Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville 22908, USA.
Annu Rev Cell Dev Biol. 1995;11:241-65. doi: 10.1146/annurev.cb.11.110195.001325.
In recent years, atomic force microscopy (AFM) has become the most rapidly developing imaging method. We summarize its recent applications in structural biology, with emphasis on high-resolution imaging, and illustrate these applications with images of cell membranes, DNA, and soluble and membrane proteins. With present technology, and at room temperature, nanometer resolution of DNA and soluble proteins is achievable, although the resolution attained on cell surfaces is more limited (10-50 nm). We suggest that high-resolution imaging of cell surfaces and very high (sub-nanometer) resolution molecular imaging requires an approach that increases specimen rigidity. Operation at cryogenic temperatures, the most promising approach, is discussed, and a cryo-AFM designed for operating at ambient pressure and liquid nitrogen temperature is described. The results include high-resolution images and evidence of increased molecular rigidity at low temperatures.
近年来,原子力显微镜(AFM)已成为发展最为迅速的成像方法。我们总结了其近期在结构生物学中的应用,重点是高分辨率成像,并通过细胞膜、DNA以及可溶性和膜蛋白的图像来说明这些应用。利用当前技术,在室温下,DNA和可溶性蛋白可实现纳米级分辨率,尽管在细胞表面获得的分辨率更为有限(10 - 50纳米)。我们认为,细胞表面的高分辨率成像以及超高(亚纳米级)分辨率分子成像需要一种提高样本刚性的方法。讨论了在低温下操作这一最具前景的方法,并描述了一种设计用于在常压和液氮温度下操作的低温AFM。结果包括高分辨率图像以及低温下分子刚性增加的证据。