Robust ab initio solution of the cryo-EM reconstruction problem at low resolution with small data sets

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aaditya V. Rangan, Leslie Greengard
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引用次数: 0

Abstract

Single particle cryo-electron microscopy has become a critical tool in structural biology over the last decade, able to achieve atomic scale resolution in three dimensional models from hundreds of thousands of (noisy) two-dimensional projection views of particles frozen at unknown orientations. This is accomplished by using a suite of software tools to (i) identify particles in large micrographs, (ii) obtain low-resolution reconstructions, (iii) refine those low-resolution structures, and (iv) finally match the obtained electron scattering density to the constituent atoms that make up the macromolecule or macromolecular complex of interest.

Here, we focus on the second stage of the reconstruction pipeline: obtaining a low resolution model from picked particle images. Our goal is to create an algorithm that is capable of ab initio reconstruction from small data sets (on the order of a few thousand selected particles). More precisely, we propose an algorithm that is robust, automatic, and fast enough that it can potentially be used to assist in the assessment of particle quality as the data is being generated during the microscopy experiment.

低分辨率小数据集低温电镜重建问题的鲁棒从头算方法
在过去的十年里,单粒子冷冻电子显微镜已经成为结构生物学中的一个关键工具,能够从数十万个(有噪声的)二维投影视图中获得在未知方向冷冻的粒子的三维模型中的原子级分辨率。这是通过使用一套软件工具来实现的:(i)识别大型显微照片中的颗粒,(ii)获得低分辨率重建,(iii)细化这些低分辨率结构,以及(iv)最终将获得的电子散射密度与组成感兴趣的大分子或大分子复合物的组成原子相匹配。在这里,我们关注重建管道的第二阶段:从拾取的粒子图像中获得低分辨率模型。我们的目标是创建一种能够从小数据集(几千个选定粒子的数量级)进行从头计算重建的算法。更准确地说,我们提出了一种稳健、自动且足够快的算法,在显微镜实验期间生成数据时,该算法可能用于帮助评估颗粒质量。
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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来源期刊
Journal of structural biology
Journal of structural biology 生物-生化与分子生物学
CiteScore
6.30
自引率
3.30%
发文量
88
审稿时长
65 days
期刊介绍: Journal of Structural Biology (JSB) has an open access mirror journal, the Journal of Structural Biology: X (JSBX), sharing the same aims and scope, editorial team, submission system and rigorous peer review. Since both journals share the same editorial system, you may submit your manuscript via either journal homepage. You will be prompted during submission (and revision) to choose in which to publish your article. The editors and reviewers are not aware of the choice you made until the article has been published online. JSB and JSBX publish papers dealing with the structural analysis of living material at every level of organization by all methods that lead to an understanding of biological function in terms of molecular and supermolecular structure. Techniques covered include: • Light microscopy including confocal microscopy • All types of electron microscopy • X-ray diffraction • Nuclear magnetic resonance • Scanning force microscopy, scanning probe microscopy, and tunneling microscopy • Digital image processing • Computational insights into structure
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