The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Science. 2010 Aug 27;329(5995):1071-5. doi: 10.1126/science.1187292.
Rational development of adenovirus vectors for therapeutic gene transfer is hampered by the lack of accurate structural information. Here, we report the x-ray structure at 3.5 angstrom resolution of the 150-megadalton adenovirus capsid containing nearly 1 million amino acids. We describe interactions between the major capsid protein (hexon) and several accessory molecules that stabilize the capsid. The virus structure also reveals an altered association between the penton base and the trimeric fiber protein, perhaps reflecting an early event in cell entry. The high-resolution structure provides a substantial advance toward understanding the assembly and cell entry mechanisms of a large double-stranded DNA virus and provides new opportunities for improving adenovirus-mediated gene transfer.
腺病毒载体的合理开发受到缺乏准确结构信息的阻碍。在这里,我们报告了包含近 100 万个氨基酸的 1.5 亿道尔顿腺病毒衣壳的 3.5 埃分辨率的 X 射线结构。我们描述了主要衣壳蛋白(六邻体)和几个稳定衣壳的辅助分子之间的相互作用。病毒结构还揭示了五邻体基底和三聚体纤维蛋白之间改变的关联,这可能反映了细胞进入的早期事件。高分辨率结构为理解大型双链 DNA 病毒的组装和细胞进入机制提供了重大进展,并为改进腺病毒介导的基因转移提供了新的机会。