Fleischli Christoph, Sirena Dominique, Lesage Guillaume, Havenga Menzo J E, Cattaneo Roberto, Greber Urs F, Hemmi Silvio
Institute of Molecular Biology, University of Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.
Crucell Holland BV, Archimedesweg 4, 2333 CN Leiden, The Netherlands.
J Gen Virol. 2007 Nov;88(Pt 11):2925-2934. doi: 10.1099/vir.0.83142-0.
We recently characterized the domains of the human cofactor protein CD46 involved in binding species B2 adenovirus (Ad) serotype 35. Here, the CD46 binding determinants are mapped for the species B1 Ad serotypes 3 and 7 and for the species B2 Ad11. Ad3, 7 and 11 bound and transduced CD46-positive rodent BHK cells at levels similar to Ad35. By using antibody-blocking experiments, hybrid CD46-CD4 receptor constructs and CD46 single point mutants, it is shown that Ad3, 7 and 11 share many of the Ad35-binding features on CD46. Both CD46 short consensus repeat domains SCR I and SCR II were necessary and sufficient for optimal binding and transgene expression, provided that they were positioned at an appropriate distance from the cell membrane. Similar to Ad35, most of the putative binding residues of Ad3, 7 and 11 were located on the same glycan-free, solvent-exposed face of the SCR I or SCR II domains, largely overlapping with the binding surface of the recently solved fiber knob Ad11-SCR I-II three-dimensional structure. Differences between species B1 and B2 Ads were documented with competition experiments based on anti-CD46 antibodies directed against epitopes flanking the putative Ad-binding sites, and with competition experiments based on soluble CD46 protein. It is concluded that the B1 and B2 species of Ad engage CD46 through similar binding surfaces.
我们最近对参与结合B2亚群35型腺病毒(Ad)的人辅助因子蛋白CD46的结构域进行了表征。在此,绘制了B1亚群3型和7型Ad以及B2亚群11型Ad的CD46结合决定簇。Ad3、7和11以与Ad35相似的水平结合并转导CD46阳性啮齿动物BHK细胞。通过抗体阻断实验、杂交CD46-CD4受体构建体和CD46单点突变体,表明Ad3、7和11在CD46上具有许多Ad35结合特征。CD46短共有重复序列结构域SCR I和SCR II对于最佳结合和转基因表达是必需且充分的,前提是它们与细胞膜保持适当的距离。与Ad35类似,Ad3、7和11的大多数推定结合残基位于SCR I或SCR II结构域的同一无糖基、溶剂暴露面上,与最近解析的纤维结Ad11-SCR I-II三维结构的结合表面大部分重叠。基于针对推定Ad结合位点侧翼表位的抗CD46抗体的竞争实验以及基于可溶性CD46蛋白的竞争实验记录了B1和B2亚群Ad之间的差异。得出的结论是,Ad的B1和B2亚群通过相似的结合表面与CD46结合。