Weis W, Brown J H, Cusack S, Paulson J C, Skehel J J, Wiley D C
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Nature. 1988 Jun 2;333(6172):426-31. doi: 10.1038/333426a0.
The three-dimensional structures of influenza virus haemagglutinins complexed with cell receptor analogues show sialic acids bound to a pocket of conserved amino acids surrounded by antibody-binding sites. Sialic acid fills the conserved pocket, demonstrating that it is the influenza virus receptor. The proximity of the antibody-binding sites suggests that antibodies neutralize virus infectivity by preventing virus-to-cell binding. The structures suggest approaches to the design of anti-viral drugs that could block attachment of viruses to cells.
与细胞受体类似物复合的流感病毒血凝素的三维结构显示,唾液酸与由抗体结合位点包围的保守氨基酸口袋结合。唾液酸填充了保守口袋,表明它是流感病毒受体。抗体结合位点的接近表明抗体通过阻止病毒与细胞结合来中和病毒感染性。这些结构为设计可阻断病毒与细胞附着的抗病毒药物提供了方法。