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通过展开二面角来明确描述病毒衣壳亚基的形状。

Explicit description of viral capsid subunit shapes by unfolding dihedrons.

机构信息

Department of General Systems Studies, The University of Tokyo, Tokyo, Japan.

Faculty of Information Science and Technology, Hokkaido University, Sapporo, Japan.

出版信息

Commun Biol. 2024 Nov 14;7(1):1509. doi: 10.1038/s42003-024-07218-x.

Abstract

Viral capsid assembly and the design of capsid-based nanocontainers critically depend on understanding the shapes and interfaces of constituent protein subunits. However, a comprehensive framework for characterizing these features is still lacking. Here, we introduce a novel approach based on spherical tiling theory that explicitly describes the 2D shapes and interfaces of subunits in icosahedral capsids. Our method unfolds spherical dihedrons defined by icosahedral symmetry axes, enabling systematic characterization of all possible subunit geometries. Applying this framework to real T = 1 capsid structures reveals distinct interface groups within this single classification, with variations in interaction patterns around 3-fold and 5-fold symmetry axes. We validate our classification through molecular docking simulations, demonstrating its consistency with physical subunit interactions. This analysis suggests different assembly pathways for capsid nucleation. Our general framework is applicable to other triangular numbers, paving the way for broader studies in structural virology and nanomaterial design.

摘要

病毒衣壳组装和基于衣壳的纳米容器的设计关键取决于对组成蛋白亚基的形状和界面的理解。然而,目前仍缺乏用于描述这些特征的综合框架。在这里,我们引入了一种基于球面平铺理论的新方法,该方法明确描述了二十面体衣壳中亚基的 2D 形状和界面。我们的方法展开由二十面体对称轴定义的球面二面体,从而能够系统地表征所有可能的亚基几何形状。将该框架应用于真实的 T=1 衣壳结构,揭示了该单一分类中存在不同的界面组,在 3 重和 5 重对称轴周围的相互作用模式存在差异。我们通过分子对接模拟验证了我们的分类,证明其与物理亚基相互作用一致。该分析表明衣壳成核有不同的组装途径。我们的通用框架适用于其他三角形数,为结构病毒学和纳米材料设计的更广泛研究铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccdf/11564659/2da2a6437edc/42003_2024_7218_Fig1_HTML.jpg

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