Marsh Michael P, Campos Samuel K, Baker Matthew L, Chen Christopher Y, Chiu Wah, Barry Michael A
Program in Structural and Computational Biology and Molecular Biophysics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
J Virol. 2006 Dec;80(23):11881-6. doi: 10.1128/JVI.01471-06. Epub 2006 Sep 20.
Recombinant human adenovirus is a useful gene delivery vector for clinical gene therapy. Minor capsid protein IX of adenovirus has been of recent interest since multiple studies have shown that modifications can be made to its C terminus to alter viral tropism or add molecular tags and/or reporter proteins. We examined the structure of an engineered adenovirus displaying the enhanced green fluorescent protein (EGFP) fused to the C terminus of protein IX. Cryoelectron microscopy and reconstruction localized the C-terminal EGFP fusion between the H2 hexon and the H4 hexon, positioned between adjacent facets, directly above the density previously assigned as protein IIIa. The original assignment of IIIa was based largely on indirect evidence, and the data presented herein support the reassignment of the IIIa density as protein IX.
重组人腺病毒是临床基因治疗中一种有用的基因递送载体。腺病毒的次要衣壳蛋白IX最近受到关注,因为多项研究表明,可以对其C末端进行修饰以改变病毒嗜性或添加分子标签和/或报告蛋白。我们研究了一种工程腺病毒的结构,该腺病毒展示了与蛋白IX的C末端融合的增强型绿色荧光蛋白(EGFP)。冷冻电子显微镜和重建技术将C末端EGFP融合定位在H2六邻体和H4六邻体之间,位于相邻小面之间,正好在先前被指定为蛋白IIIa的密度上方。IIIa的原始归属很大程度上基于间接证据,本文提供的数据支持将IIIa密度重新归属为蛋白IX。