High-Resolution Cryo-Scanning Electron Microscopy of Macromolecular Complexes

Sebastian Tacke, F. Lucas, J. Woodward, H. Gross, R. Wepf
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引用次数: 2

Abstract

The beauty of Scanning Electron Microscopy (SEM) is its power to describe and integrate structural details, mainly surface related details, within the context of a complex system. Its unique ability compared to other Electron Microscopy techniques (STEM & TEM) is that handling and imaging of bulk samples is in principal possible and hence sectioning, thinning or replicating of the specimen is not essential when surfaces structures are to be investigated. With the introduction of Field Emission SEM (FESEM), especially in combination with improvements to the signal detection efficiency ("in-lens" detection and new type of detectors), high resolution SEM (HRSEM) has become a powerful approach to describe structural details even down to macromolecular dimensions (1-2nm) for structural studies in Biology and soft-material science.
大分子复合物的高分辨率冷冻扫描电镜
扫描电子显微镜(SEM)的优点在于它能够在复杂系统的背景下描述和整合结构细节,主要是与表面相关的细节。与其他电子显微镜技术(STEM和TEM)相比,其独特的能力在于,处理和成像大量样品基本上是可能的,因此在研究表面结构时,不需要对样品进行切片、减薄或复制。随着场发射扫描电镜(FESEM)的引入,特别是结合信号检测效率的提高(“透镜内”检测和新型探测器),高分辨率扫描电镜(HRSEM)已经成为描述结构细节的有力方法,甚至可以达到大分子尺寸(1-2nm),用于生物学和软材料科学的结构研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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