de Pablo Pedro J, San Martín Carmen
Departamento de Física de la Materia Condensada, Universidad Autónoma de Madrid and IFIMAC, 28049 Madrid, Spain.
Departamento de Estructura de Macromoléculas, Centro Nacional de Biotecnología (CNB-CSIC), Darwin 3, 28049 Madrid, Spain.
Curr Opin Virol. 2022 Feb;52:112-122. doi: 10.1016/j.coviro.2021.11.006. Epub 2021 Dec 11.
Understanding adenovirus assembly and disassembly poses many challenges due to the virion complexity. A distinctive feature of adenoviruses is the large amount of virus-encoded proteins packed together with the dsDNA genome. Cryo-electron microscopy (cryo-EM) structures are broadening our understanding of capsid variability along evolution, but little is known about the organization of the non-icosahedral nucleoproteic core and its influence in adenovirus function. Atomic force microscopy (AFM) probes the biomechanics of virus particles, while simultaneously inducing and monitoring their disassembly in real time. Synergistic combination of AFM with EM shows that core proteins play unexpected key roles in maturation and entry, and uncoating dynamics are finely tuned to ensure genome release at the appropriate time and place for successful infection.
由于腺病毒粒子的复杂性,了解腺病毒的组装和拆卸面临诸多挑战。腺病毒的一个显著特征是大量病毒编码蛋白与双链DNA基因组一起包装。冷冻电子显微镜(cryo-EM)结构正在拓宽我们对衣壳沿进化过程中变异性的理解,但对于非二十面体核蛋白核心的组织及其对腺病毒功能的影响知之甚少。原子力显微镜(AFM)可探测病毒颗粒的生物力学,同时实时诱导并监测其拆卸过程。AFM与EM的协同结合表明,核心蛋白在成熟和进入过程中发挥着意想不到的关键作用,并且脱壳动力学经过精细调节,以确保基因组在合适的时间和地点释放,从而成功感染。