Key Laboratory for Microstructural Material Physics of Hebei Province, School of Science, Yanshan University, Qinhuangdao, China.
The Sixth Laboratory, National Vaccine and Serum Institute, Beijing, China.
Proteins. 2021 Oct;89(10):1365-1375. doi: 10.1002/prot.26157. Epub 2021 Jun 14.
The coxsackievirus A16 (CVA16) is a highly contagious virus that causes the hand, foot, and mouth disease, which seriously threatens the health of children. At present, there are still no available antiviral drugs or effective treatments against the infection of CVA16, and thus it is of great significance to develop anti-CVA16 vaccines. However, the intrinsic uncoating property of the capsid may destroy the neutralizing epitopes and influence its immunogenicity, which hinders the vaccine developments. In the present work, the functional-quantity-based elastic network model analysis method developed by our group was extended to combine with group theory to investigate the uncoating motions of the CVA16 capsid, and then the functionally key residues controlling the uncoating motions were identified by our functional-quantity-based perturbation method. Several motion modes encoded in the topological structure of the capsid were revealed to be responsible for the uncoating of CVA16 particle. These modes predominantly contribute to the fluctuation of the gyration radius of the capsid. Then, by using the perturbation method, four clusters of key sites involved in the uncoating motions were identified, whose perturbations induce significant changes in the fluctuation of the gyration radius. These key residues are mainly located at the 2-fold channels, the quasi 3-fold channels, the bottom of the canyons, and the inter-subunit interfaces around the 3-fold axes. Our studies are helpful for better understanding the uncoating mechanism of the CVA16 capsid and provide potential target sites to prevent the uncoating motions, which is valuable for the vaccine design against CVA16.
柯萨奇病毒 A16(CVA16)是一种高度传染性病毒,可引起手足口病,严重威胁儿童健康。目前,尚无针对 CVA16 感染的可用抗病毒药物或有效治疗方法,因此开发抗 CVA16 疫苗具有重要意义。然而,衣壳的内在脱壳特性可能会破坏中和表位并影响其免疫原性,从而阻碍疫苗的开发。在本工作中,我们小组开发的基于功能量的弹性网络模型分析方法扩展到结合群论来研究 CVA16 衣壳的脱壳运动,然后通过我们的基于功能量的扰动方法鉴定控制脱壳运动的功能关键残基。揭示了衣壳拓扑结构中编码的几种运动模式,这些模式负责 CVA16 颗粒的脱壳。这些模式主要有助于衣壳回旋半径的波动。然后,通过使用扰动方法,鉴定了参与脱壳运动的四个关键位点簇,其扰动会导致回旋半径波动发生显著变化。这些关键残基主要位于 2 倍通道、准 3 倍通道、峡谷底部和 3 倍轴周围的亚基界面。我们的研究有助于更好地理解 CVA16 衣壳的脱壳机制,并为防止脱壳运动提供潜在的靶位,这对于针对 CVA16 的疫苗设计具有重要价值。