Castón José R
Department of Macromolecular Structure, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Subcell Biochem. 2024;105:55-78. doi: 10.1007/978-3-031-65187-8_2.
Viruses are elegant macromolecular assemblies and constitute a paradigm of the economy of genomic resources; they must use simple general principles to complete their life cycles successfully. Viruses need only one or a few different capsid structural subunits to build an infectious particle, which is possible for two reasons: extensive use of symmetry and built-in conformational flexibility. Although viruses come in many shapes and sizes, two major symmetric assemblies are found: icosahedral and helical. The enormous diversity of virus structures appears to be derived from one or a limited number of basic schemes that became more complex by consecutive incorporation of additional structural elements. The intrinsic structural polymorphism of the viral proteins results in dynamic capsids. The study of virus structures is required to understand structure-function relationships, including those related to morphogenesis and antigenicity, among many others. These structural foundations can be extended to other macromolecular complexes that control many fundamental processes in biology.
病毒是精巧的大分子组装体,构成了基因组资源经济性的典范;它们必须运用简单的通用原则才能成功完成其生命周期。病毒仅需一种或几种不同的衣壳结构亚基就能构建出感染性颗粒,这之所以可行有两个原因:广泛利用对称性以及固有的构象灵活性。尽管病毒有多种形状和大小,但主要发现了两种对称组装形式:二十面体和螺旋形。病毒结构的巨大多样性似乎源自一种或有限数量的基本模式,这些模式通过连续纳入额外的结构元件而变得更加复杂。病毒蛋白固有的结构多态性导致衣壳具有动态性。研究病毒结构对于理解结构与功能的关系是必要的,这其中包括与形态发生和抗原性等相关的关系。这些结构基础可以扩展到控制生物学中许多基本过程的其他大分子复合物。