Madisch Ijad, Hofmayer Soeren, Moritz Christian, Grintzalis Alexander, Hainmueller Jens, Pring-Akerblom Patricia, Heim Albert
Institut für Virologie, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.
J Virol. 2007 Aug;81(15):8270-81. doi: 10.1128/JVI.00048-07. Epub 2007 May 23.
The penton base is a major capsid protein of human adenoviruses (HAdV) which forms the vertices of the capsid and interacts with hexon and fiber protein. Two hypervariable loops of the penton are exposed on the capsid surface. Sequences of these and 300 adjacent amino acid residues of all 51 HAdV and closely related simian adenoviruses were studied. Adjacent sequences and predicted overall secondary structure were conserved. Phylogenetic analysis revealed clustering corresponding to the HAdV species and recombination events in the origin of HAdV prototypes. All HAdV except serotypes 40 and 41 of species F exhibited an integrin binding RGD motif in the second loop. The lengths of the loops (HVR1 and RGD loops) varied significantly between HAdV species with the longest RGD loop observed in species C and the longest HVR1 in species B. Long loops may permit the insertion of motifs that modify tissue tropism. Genetic analysis of HAdV prime strain p17'H30, a neutralization variant of HAdV-D17, indicated the significance of nonhexon neutralization epitopes for HAdV immune escape. Fourteen highly conserved motifs of the penton base were analyzed by site-directed mutagenesis of HAdV-D8 and tested for sustained induction of early cytopathic effects. Thus, three new motifs essential for penton base function were identified additionally to the RGD site, which interacts with a secondary cellular receptor responsible for internalization. Therefore, our penton primary structure data and secondary structure modeling in combination with the recently published fiber knob sequences may permit the rational design of tissue-specific adenoviral vectors.
五邻体基底是人类腺病毒(HAdV)的一种主要衣壳蛋白,它形成衣壳的顶点,并与六邻体和纤维蛋白相互作用。五邻体的两个高变环暴露在衣壳表面。研究了所有51种HAdV以及与之密切相关的猿猴腺病毒的这些环及其300个相邻氨基酸残基的序列。相邻序列和预测的整体二级结构是保守的。系统发育分析揭示了与HAdV种类相对应的聚类以及HAdV原型起源中的重组事件。除F种的40型和41型血清型外,所有HAdV在第二个环中都表现出整合素结合RGD基序。不同HAdV种类之间环(高变环1和RGD环)的长度差异显著,在C种中观察到最长的RGD环,在B种中观察到最长的高变环1。长环可能允许插入修饰组织嗜性的基序。对HAdV-D17的中和变体HAdV原代菌株p17'H30的遗传分析表明,非六邻体中和表位对HAdV免疫逃逸具有重要意义。通过对HAdV-D8进行定点诱变,分析了五邻体基底的14个高度保守基序,并测试了其对早期细胞病变效应的持续诱导作用。因此,除了与负责内化的二级细胞受体相互作用的RGD位点外,还额外鉴定出了三个对五邻体基底功能至关重要的新基序。因此,我们的五邻体一级结构数据和二级结构模型,结合最近发表的纤维结序列,可能有助于合理设计组织特异性腺病毒载体。