Development of Nano-Biology with Atomic Force Microscopy

K. Takeyasu, Katashi Deguchi, Jamie L. Gilmore, J. Hejna
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Abstract

The first observation of double-stranded DNA by atomic force microscopy in the late 1980’s greatly encouraged many biological researchers to jump into the nano-world. Here we briefly review the history of how AFM has been utilized to reveal nanometer-scale structures of DNA-protein complexes, and we highlight key technical developments that have accelerated applications of AFM to molecular biology, physiology, biophysics, and cell biology. Biology is a visual science. Understanding the ‘biological events’ around us through visualization and observation has always been a fundamental part of biological scientific inquiry. Since the early days in the 17th century, biological investigations of the fundamental components of biological systems have relied on microscopes, the resolution of which is limited to one half the wavelength of light. Electron microscopy (EM), invented in the 1920-1930’s, brought a hundred times greater resolution than the light microscope, and it continues to enable us to visualize biological materials in the nanometer range [1]. However, EM requires special specimen preparation and operational constraints, e.g., coating the sample with a fine layer of gold and observing it under vacuum. These limitations were in large part circumvented in the 1980’s by an altogether new concept. Shortly after Binnig invented atomic force microscopy (AFM) [2], Hansma [3] proposed many possible uses for AFM in biology [3]. However it took almost 20 years for it to become an indispensable technique in biological research that allows observations in solution without fixation of the specimen. Commercially available instruments equipped with a scanning method known as the tapping mode [4,5], have yielded unprecedented views of biological materials such as DNA and proteins in their native state. The subsequent invention of high-speed AFM [6], which can scan biological samples in solution with sub-second temporal resolution, was a landmark accomplishment that has contributed greatly to the establishment of nanobiology as a major field in bioscience [7].
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原子力显微镜在纳米生物学研究中的进展
20世纪80年代末,原子力显微镜首次观察到双链DNA,极大地鼓舞了许多生物学研究人员进入纳米世界。在这里,我们简要回顾了原子力显微镜用于揭示dna -蛋白质复合物纳米结构的历史,并重点介绍了加速原子力显微镜在分子生物学、生理学、生物物理学和细胞生物学中的应用的关键技术发展。生物学是一门视觉科学。通过可视化和观察来理解我们周围的“生物事件”一直是生物科学探索的基本组成部分。自17世纪早期以来,对生物系统基本组成部分的生物学研究一直依赖于显微镜,其分辨率仅限于光波长的一半。电子显微镜(EM)发明于20世纪20年代至30年代,它带来了比光学显微镜高100倍的分辨率,并继续使我们能够在纳米范围内可视化生物材料[1]。然而,EM需要特殊的样品制备和操作限制,例如,在样品上涂上一层细金并在真空下观察。在20世纪80年代,一种全新的概念在很大程度上规避了这些限制。在binning发明原子力显微镜(atomic force microscopy, AFM)[2]后不久,Hansma[3]提出了AFM在生物学中的许多可能用途[3]。然而,它花了将近20年的时间才成为生物学研究中不可或缺的技术,可以在溶液中观察而无需固定标本。商用仪器配备了一种被称为敲击模式的扫描方法[4,5],已经产生了前所未有的生物材料,如DNA和蛋白质在其天然状态的视图。随后发明的高速AFM[6]能够以亚秒级的时间分辨率扫描溶液中的生物样品,这是一项里程碑式的成就,为纳米生物学作为生物科学的一个主要领域的建立做出了巨大贡献[7]。
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