Weisenhorn A L, Gaub H E, Hansma H G, Sinsheimer R L, Kelderman G L, Hansma P K
Dept. of Physics, University of California, Santa Barbara 93106.
Scanning Microsc. 1990 Sep;4(3):511-6.
The combination of an (AFM) atomic force microscope together with microfabricated cantilevers that have integrated tips opens many possibilities for imaging systems of great importance in biology. We have imaged single-stranded 25mer DNA that was adsorbed on treated mica or that was covalently bound with a crosslinker to a polymerized Langmuir-Blodgett (LB) film, the top monolayer of a bilayer system. At low magnification the AFM shows cracks between solid domains, like in an image taken with a fluorescence microscope. At higher magnification, however, the AFM reveals much finer cracks and at still higher magnification it reveals rows of individual molecules in the polymerized LB film with a spacing of 0.45 nm. We have also imaged a LB film consisting of lipids in which 4% of the lipids had hapten molecules chemically bound to the lipid headgroups. Specific antibodies can then bind to these hapten molecules and be imaged with the AFM. This points to the possibility of using the AFM to monitor selective antibody binding.
原子力显微镜(AFM)与集成了探针的微加工悬臂相结合,为生物学中极为重要的成像系统开辟了诸多可能性。我们对吸附在经过处理的云母上或通过交联剂共价结合到聚合朗缪尔-布洛杰特(LB)膜(双层系统的顶层单分子层)上的单链25聚体DNA进行了成像。在低放大倍数下,AFM显示出固体区域之间的裂缝,就如同用荧光显微镜拍摄的图像一样。然而,在更高放大倍数下,AFM揭示出更细微的裂缝,在更高的放大倍数下,它能显示出聚合LB膜中一排排间距为0.45纳米的单个分子。我们还对由脂质组成的LB膜进行了成像,其中4%的脂质在其头部基团上化学结合了半抗原分子。然后,特异性抗体可以结合到这些半抗原分子上,并通过AFM进行成像。这表明利用AFM监测选择性抗体结合的可能性。