Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
J Virol. 2018 Aug 29;92(18). doi: 10.1128/JVI.00821-18. Print 2018 Sep 15.
The herpesvirus capsid assembles in the nucleus as an immature procapsid precursor built around viral scaffold proteins. The event that initiates procapsid maturation is unknown, but it is dependent upon activation of the VP24 internal protease. Scaffold cleavage triggers angularization of the shell and its decoration with the VP26 and pUL25 capsid-surface proteins. In both the procapsid and mature angularized capsid, the apical region of the major capsid protein (VP5) is surface exposed. We investigated whether the VP5 apical region contributes to intracellular transport dynamics following entry into primary sensory neurons and also tested the hypothesis that conserved negatively charged amino acids in the apical region contribute to VP26 acquisition. To our surprise, neither hypothesis proved true. Instead, mutation of glutamic acid residues in the apical region delayed viral propagation and induced focal capsid accumulations in nuclei. Examination of capsid morphogenesis based on epitope unmasking, capsid composition, and ultrastructural analysis indicated that these clusters consisted of procapsids. The results demonstrate that, in addition to established events that occur inside the capsid, the exterior capsid shell promotes capsid morphogenesis and maturation. Herpesviruses assemble capsids and encapsidate their genomes by a process that is unlike those of other mammalian viruses but is similar to those of some bacteriophage. Many important aspects of herpesvirus morphogenesis remain enigmatic, including how the capsid shell matures into a stable angularized configuration. Capsid maturation is triggered by activation of a protease that cleaves an internal protein scaffold. We report on the fortuitous discovery that a region of the major capsid protein that is exposed on the outer surface of the capsid also contributes to capsid maturation, demonstrating that the morphogenesis of the capsid shell from its procapsid precursor to the mature angularized form is dependent upon internal and external components of the megastructure.
疱疹病毒衣壳在核内作为不成熟的原衣壳前体组装,该前体围绕病毒支架蛋白构建。启动原衣壳成熟的事件尚不清楚,但它依赖于 VP24 内部蛋白酶的激活。支架切割触发壳的角状化及其与 VP26 和 pUL25 衣壳表面蛋白的装饰。在原衣壳和成熟的角状衣壳中,主要衣壳蛋白 (VP5) 的顶端区域暴露在表面。我们研究了 VP5 顶端区域是否有助于进入原感觉神经元后的细胞内运输动态,还测试了保守的顶端区域带负电荷氨基酸是否有助于 VP26 获得的假设。令我们惊讶的是,这两个假设都没有被证明是正确的。相反,突变顶端区域的谷氨酸残基会延迟病毒的繁殖,并在核内诱导焦点衣壳聚集。基于表位暴露、衣壳组成和超微结构分析的衣壳形态发生研究表明,这些簇由原衣壳组成。结果表明,除了发生在衣壳内部的既定事件外,外壳还促进了衣壳形态发生和成熟。疱疹病毒通过与其他哺乳动物病毒不同但与某些噬菌体相似的过程组装衣壳并将其基因组包裹起来。疱疹病毒形态发生的许多重要方面仍然是个谜,包括衣壳壳如何成熟为稳定的角状结构。衣壳成熟是由激活一种切割内部蛋白支架的蛋白酶触发的。我们报告了一个偶然的发现,即衣壳上暴露在外表面的主要衣壳蛋白的一个区域也有助于衣壳成熟,这表明从原衣壳前体到成熟的角状形式的衣壳壳的形态发生依赖于巨型结构的内部和外部组件。