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2D hybrid analysis: Approach for building three-dimensional atomic model by electron microscopy image matching

机译:二维混合分析:通过电子显微镜图像匹配建立三维原子模型的方法

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摘要

In this study, we develop an approach termed “2D hybrid analysis” for building atomic models by image matching from electron microscopy (EM) images of biological molecules. The key advantage is that it is applicable to flexible molecules, which are difficult to analyze by 3DEM approach. In the proposed approach, first, a lot of atomic models with different conformations are built by computer simulation. Then, simulated EM images are built from each atomic model. Finally, they are compared with the experimental EM image. Two kinds of models are used as simulated EM images: the negative stain model and the simple projection model. Although the former is more realistic, the latter is adopted to perform faster computations. The use of the negative stain model enables decomposition of the averaged EM images into multiple projection images, each of which originated from a different conformation or orientation. We apply this approach to the EM images of integrin to obtain the distribution of the conformations, from which the pathway of the conformational change of the protein is deduced.
机译:在这项研究中,我们开发了一种称为“ 2D混合分析”的方法,用于通过生物分子的电子显微镜(EM)图像的图像匹配来建立原子模型。关键优势在于它适用于柔性分子,这些分子很难通过3DEM方法进行分析。在提出的方法中,首先,通过计算机模拟建立了许多具有不同构象的原子模型。然后,从每个原子模型构建仿真的EM图像。最后,将它们与实验EM图像进行比较。两种模型用作模拟EM图像:负染模型和简单投影模型。尽管前者更现实,但后者被采用来执行更快的计算。负染色模型的使用可以将平均的EM图像分解为多个投影图像,每个投影图像都源自不同的构象或方向。我们将此方法应用于整联蛋白的EM图像,以获取构象的分布,从中推导出蛋白质构象变化的途径。

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