Overview and applications of map and model validation tools in the CCP-EM software suite†

IF 3.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Agnel Praveen Joseph, Sony Malhotra, Tom Burnley and Martyn D. Winn
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引用次数: 0

Abstract

Cryogenic electron microscopy (cryo-EM) has recently been established as a powerful technique for solving macromolecular structures. Although the best resolutions achievable are improving, a significant majority of data are still resolved at resolutions worse than 3 ?, where it is non-trivial to build or fit atomic models. The map reconstructions and atomic models derived from the maps are also prone to errors accumulated through the different stages of data processing. Here, we highlight the need to evaluate both model geometry and fit to data at different resolutions. Assessment of cryo-EM structures from SARS-CoV-2 highlights a bias towards optimising the model geometry to agree with the most common conformations, compared to the agreement with data. We present the CoVal web service which provides multiple validation metrics to reflect the quality of atomic models derived from cryo-EM data of structures from SARS-CoV-2. We demonstrate that further refinement can lead to improvement of the agreement with data without the loss of geometric quality. We also discuss the recent CCP-EM developments aimed at addressing some of the current shortcomings.

Abstract Image

CCP-EM软件套件中地图和模型验证工具的概述和应用
低温电子显微镜(cryo-EM)是近年来研究大分子结构的一种强有力的技术。尽管可实现的最佳分辨率正在提高,但绝大多数数据的分辨率仍然低于3 ?,在这种情况下,构建或拟合原子模型是非常重要的。从地图中提取的地图重建和原子模型也容易在数据处理的不同阶段积累错误。在这里,我们强调需要评估模型几何形状和适合不同分辨率的数据。对SARS-CoV-2的低温电镜结构的评估突出了与数据一致相比,优化模型几何形状以符合最常见构象的倾向。我们提出了CoVal web服务,该服务提供了多个验证指标,以反映从SARS-CoV-2结构的低温电镜数据中得出的原子模型的质量。我们证明了进一步的细化可以在不损失几何质量的情况下改善与数据的一致性。我们还讨论了最近CCP-EM的发展,旨在解决当前的一些缺点。
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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
自引率
0.00%
发文量
259
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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