Departamento de Física de la Materia Condensada, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Sci Rep. 2013;3:1434. doi: 10.1038/srep01434.
The standard pathway for virus infection of eukaryotic cells requires disassembly of the viral shell to facilitate release of the viral genome into the host cell. Here we use mechanical fatigue, well below rupture strength, to induce stepwise disruption of individual human adenovirus particles under physiological conditions, and simultaneously monitor disassembly in real time. Our data show the sequence of dismantling events in individual mature (infectious) and immature (noninfectious) virions, starting with consecutive release of vertex structures followed by capsid cracking and core exposure. Further, our experiments demonstrate that vertex resilience depends inextricably on maturation, and establish the relevance of penton vacancies as seeding loci for virus shell disruption. The mechanical fatigue disruption route recapitulates the adenovirus disassembly pathway in vivo, as well as the stability differences between mature and immature virions.
真核细胞中病毒感染的标准途径需要病毒外壳的解体,以促进病毒基因组释放到宿主细胞中。在这里,我们在生理条件下使用远低于断裂强度的机械疲劳来诱导单个人类腺病毒颗粒的逐步解体,并实时监测解体过程。我们的数据显示了单个成熟(感染性)和不成熟(非感染性)病毒粒子的拆卸事件序列,从顶点结构的连续释放开始,然后是衣壳的破裂和核心的暴露。此外,我们的实验证明,顶点的弹性与成熟度密不可分,并且确立了五邻体空位作为病毒外壳解体的种子位置的相关性。机械疲劳破坏途径再现了体内腺病毒的解体途径,以及成熟和不成熟病毒粒子之间的稳定性差异。