利用基于物理的方法从低温电子显微镜数据中获得更好的结构模型。

IF 3 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Hande Boyaci Selcuk, Gabriella Reggiano, Jacob Robson-Tull, Lichirui Zhang, João P G L M Rodrigues
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引用次数: 0

摘要

冷冻电子显微镜现在可以常规地为各种生物系统提供原子分辨率结构。这些结构的相关性和价值直接关系到它们帮助合理化实验观测值的能力,这反过来又取决于密度图中构建的模型的质量。将传统的模型构建工具与基于物理的方法相结合,如对接、仿真和现代力场,已被证明可以提高所得结构的质量。在这里,我们调查了这些混合方法的前景,强调了它们对中低分辨率数据集以及小分子结构的有用性,并提出了社区将受益于它们在模型构建和改进工作流程中的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Towards better structural models from cryo-electron microscopy data with physics-based methods.

Cryo-electron microscopy can now routinely deliver atomic resolution structures for a variety of biological systems. The relevance and value of these structures are directly related to their ability to help rationalize experimental observables, which in turn depend on the quality of the model built into the density map. Coupling traditional model-building tools with physics-based methods, such as docking, simulation, and modern force fields, has been shown to improve the quality of the resulting structures. Here, we survey the landscape of these hybrid approaches, highlighting their usefulness for medium- and low-resolution datasets, as well as for structures of small molecules, and make the argument that the community stands to benefit from their inclusion in model building and refinement workflows.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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