Hörber J K, Häberle W, Ohnesorge F, Binnig G, Liebich H G, Czerny C P, Mahnel H, Mayr A
Max-Planck-Institut für Medizinische Forschung, Heidelberg, Federal Republic of Germany.
Scanning Microsc. 1992 Dec;6(4):919-29; discussion 929-30.
Membrane structures of different types of cells are imaged in the nanometer regime by scanning force microscopy (SFM). The images are compared to those obtained with a scanning electron microscope (SEM). The SFM imaging can be done on the outer cell membrane under conditions that keep the cells alive in aqueous solutions. This opens up the possibility of observing the kinematics of the structures that determine the interaction of a cell with its environment. Therefore, STM observations, together with information obtained with the electron microscope, open up new ways of studying the development of biological structures. With the currently possible resolution, the SFM gives access to processes such as antibody binding or endo- and exocytosis, including processes correlated to the infection of cells by viruses.
通过扫描力显微镜(SFM)在纳米尺度下对不同类型细胞的膜结构进行成像。将这些图像与用扫描电子显微镜(SEM)获得的图像进行比较。SFM成像可以在保持细胞在水溶液中存活的条件下对细胞外膜进行。这为观察决定细胞与其环境相互作用的结构的运动学提供了可能性。因此,扫描隧道显微镜(STM)观察以及从电子显微镜获得的信息,为研究生物结构的发育开辟了新途径。以目前可能达到的分辨率,SFM能够观察到诸如抗体结合或胞吞和胞吐等过程,包括与病毒感染细胞相关的过程。