Spatiotemporal resolution in high-speed atomic force microscopy for studying biological macromolecules in action

被引:18
|
作者
Umeda, Kenichi [1 ]
McArthur, Steven J. [1 ]
Kodera, Noriyuki [1 ]
机构
[1] Kanazawa Univ, Nano Life Sci Inst WPI NanoLSI, Kanazawa 9201192, Japan
关键词
atomic force microscopy; single-molecule imaging; biophysics; proteins; nucleic acids; biomolecules; SILICON (111)-(7X7) SURFACE; PROTEIN INTERACTIONS; DYNAMIC-BEHAVIOR; REAL-TIME; AFM; REVEALS; BACTERIORHODOPSIN; RECONSTRUCTION; VISUALIZATION; LOCALIZATION;
D O I
10.1093/jmicro/dfad011
中图分类号
TH742 [显微镜];
学科分类号
摘要
High-speed atomic force microscopy (HS-AFM) is a unique approach that allows direct real-time visualization of biological macromolecules in action under near-physiological conditions, without any chemical labeling. Typically, the temporal resolution is sub-100 ms, and the spatial resolution is 2-3 nm in the lateral direction and similar to 0.1 nm in the vertical direction. A wide range of biomolecular systems and their dynamic processes have been studied by HS-AFM, providing deep mechanistic insights into how biomolecules function. However, the level of mechanistic detail gleaned from an HS-AFM experiment critically depends on the spatiotemporal resolution of the system. In this review article, we explain the principle of HS-AFM and describe how the resolution is determined. We also discuss recent attempts to improve the resolution of HS-AFM to further extend the observable range of biological phenomena.
引用
收藏
页码:151 / 161
页数:11
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