Bizebard T, Gigant B, Rigolet P, Rasmussen B, Diat O, Bösecke P, Wharton S A, Skehel J J, Knossow M
Laboratoire de Biologie Structurale, UMR 9920, CNRS-Université Paris-Sud, Gif-sur-Yvette, France.
Nature. 1995 Jul 6;376(6535):92-4. doi: 10.1038/376092a0.
Haemagglutinin (HA) is the influenza surface glycoprotein that interacts with infectivity-neutralizing antibodies. As a consequence of this immune pressure, it is the variable virus component, which is important in antigenic drift, that results in recurrent epidemics of influenza. We have determined the crystallographic structure of a complex formed between the antigen-binding fragment (Fab) of a neutralizing antibody and the membrane-distal domain ('HA top') of a HA subunit prepared from HA in its membrane-fusion-active conformation. A dramatic change is seen in the structure of the Fab-combining site on complex formation. Our results indicate that neutralization of infectivity by this antibody involves the inhibition of receptor binding, and demonstrate how influenza virus can maintain its conserved receptor-binding site despite the immune selective pressure for change in this region of the molecule; they also contribute to a complete description of the endosomal pH-induced fusion-active HA structure.
血凝素(HA)是流感病毒的表面糖蛋白,可与感染性中和抗体相互作用。由于这种免疫压力,它是可变的病毒成分,在抗原漂移中起重要作用,导致流感反复流行。我们已经确定了一种复合物的晶体结构,该复合物由中和抗体的抗原结合片段(Fab)与从处于膜融合活性构象的HA制备的HA亚基的膜远端结构域(“HA顶部”)形成。复合物形成时,Fab结合位点的结构发生了显著变化。我们的结果表明,该抗体对感染性的中和作用涉及对受体结合的抑制,并证明了流感病毒如何在该分子区域存在免疫选择压力要求发生变化的情况下仍能维持其保守的受体结合位点;它们还有助于完整描述内体pH诱导的融合活性HA结构。