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分析病毒结构的几何形状和动力学:基于 Alpha 形状理论、正则模态分析和泊松-玻尔兹曼理论的计算方法综述。

Analyzing the Geometry and Dynamics of Viral Structures: A Review of Computational Approaches Based on Alpha Shape Theory, Normal Mode Analysis, and Poisson-Boltzmann Theories.

机构信息

Institute for Arctic and Marine Biology, Department of Biosciences, Fisheries, and Economics, UiT The Arctic University of Norway, 9037 Tromso, Norway.

Institut Pasteur, Université Paris-Cité and CNRS, UMR 3528, Unité Architecture et Dynamique des Macromolécules Biologiques, 75015 Paris, France.

出版信息

Viruses. 2023 Jun 13;15(6):1366. doi: 10.3390/v15061366.

Abstract

The current SARS-CoV-2 pandemic highlights our fragility when we are exposed to emergent viruses either directly or through zoonotic diseases. Fortunately, our knowledge of the biology of those viruses is improving. In particular, we have more and more structural information on virions, i.e., the infective form of a virus that includes its genomic material and surrounding protective capsid, and on their gene products. It is important to have methods that enable the analyses of structural information on such large macromolecular systems. We review some of those methods in this paper. We focus on understanding the geometry of virions and viral structural proteins, their dynamics, and their energetics, with the ambition that this understanding can help design antiviral agents. We discuss those methods in light of the specificities of those structures, mainly that they are huge. We focus on three of our own methods based on the alpha shape theory for computing geometry, normal mode analyses to study dynamics, and modified Poisson-Boltzmann theories to study the organization of ions and co-solvent and solvent molecules around biomacromolecules. The corresponding software has computing times that are compatible with the use of regular desktop computers. We show examples of their applications on some outer shells and structural proteins of the West Nile Virus.

摘要

当前的 SARS-CoV-2 大流行凸显了我们在直接或通过动物源性病原体暴露于新发病毒时的脆弱性。幸运的是,我们对这些病毒的生物学认识正在不断提高。特别是,我们对病毒粒子(即病毒的感染形式,包括其基因组材料和周围的保护性衣壳)及其基因产物有了越来越多的结构信息。拥有能够分析此类大型大分子系统结构信息的方法非常重要。本文综述了其中的一些方法。我们专注于理解病毒粒子和病毒结构蛋白的几何形状、它们的动力学和它们的能量学,以期这种理解可以帮助设计抗病毒药物。我们根据这些结构的特异性来讨论这些方法,主要是它们非常巨大。我们专注于我们自己的三种方法,基于 alpha 形状理论进行计算几何、正常模式分析研究动力学以及修改后的泊松-玻尔兹曼理论研究离子和共溶剂以及溶剂分子在生物大分子周围的组织。相应的软件具有与使用常规台式计算机兼容的计算时间。我们展示了它们在西尼罗河病毒的一些外壳和结构蛋白上的应用示例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fae/10300701/df608b81d072/viruses-15-01366-g001.jpg

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