用二维类平均法分析分子复合物图像的负染色透射电子显微镜

John R. Gallagher, Alexander J. Kim, Neetu M. Gulati, Audray K. Harris
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引用次数: 16

摘要

负染色透射电子显微镜(EM)是一种提供纳米分辨率的大分子图像的技术,已有大约60年的历史。低温电子显微镜图像处理的发展使从平均大量粒子中获得的信息最大化。这些发展现在可以应用到负染色图像分析,以确定区域水平的分子结构(10至20 Å)比原子分辨率冷冻电镜更快,更有效。利用醋酸铀酰染色的流感血凝素与Fab 441D6结合的分子复合物,我们描述了一种简单而有效的方法,可以用SerialEM收集数百张显微照片。使用RELION,我们说明了如何自动选择和分类成千上万的复合物,以准确地描述这种非常规血凝素头结构域表位的结构域水平拓扑结构。通过与相同复合体的低温电镜密度图进行比较,我们发现这种阴性染色方法可以很容易地回答有关表位定位和构象异质性的问题。©2019作者。
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Negative-Stain Transmission Electron Microscopy of Molecular Complexes for Image Analysis by 2D Class Averaging

Negative-stain transmission electron microscopy (EM) is a technique that has provided nanometer resolution images of macromolecules for about 60 years. Developments in cryo-EM image processing have maximized the information gained from averaging large numbers of particles. These developments can now be applied back to negative-stain image analysis to ascertain domain level molecular structure (10 to 20 Å) more quickly and efficiently than possible by atomic resolution cryo-EM. Using uranyl acetate stained molecular complexes of influenza hemagglutinin bound to Fab 441D6, we describe a simple and efficient means to collect several hundred micrographs with SerialEM. Using RELION, we illustrate how tens of thousands of complexes can be auto-picked and classified to accurately describe the domain level topology of this unconventional hemagglutinin head-domain epitope. By comparing to the cryo-EM density map of the same complex, we show that questions about epitope mapping and conformational heterogeneity can readily be answered by this negative-stain method. © 2019 The Authors.

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来源期刊
Current Protocols in Microbiology
Current Protocols in Microbiology Immunology and Microbiology-Parasitology
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期刊介绍: Current Protocols in Microbiology provides detailed, step-by-step instructions for analyzing bacteria, animal and plant viruses, fungi, protozoans and other microbes. It offers updated coverage of emerging technologies and concepts, such as biofilms, quorum sensing and quantitative PCR, as well as proteomic and genomic methods. It is the first comprehensive source of high-quality microbiology protocols that reflects and incorporates the new mandates and capabilities of this robust and rapidly evolving discipline.
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