Kadam Rameshwar U, Wilson Ian A
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037.
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037;
Proc Natl Acad Sci U S A. 2017 Jan 10;114(2):206-214. doi: 10.1073/pnas.1617020114. Epub 2016 Dec 21.
The broad-spectrum antiviral drug Arbidol shows efficacy against influenza viruses by targeting the hemagglutinin (HA) fusion machinery. However, the structural basis of the mechanism underlying fusion inhibition by Arbidol has remained obscure, thereby hindering its further development as a specific and optimized influenza therapeutic. We determined crystal structures of Arbidol in complex with influenza virus HA from pandemic 1968 H3N2 and recent 2013 H7N9 viruses. Arbidol binds in a hydrophobic cavity in the HA trimer stem at the interface between two protomers. This cavity is distal to the conserved epitope targeted by broadly neutralizing stem antibodies and is ∼16 Å from the fusion peptide. Arbidol primarily makes hydrophobic interactions with the binding site but also induces some conformational rearrangements to form a network of inter- and intraprotomer salt bridges. By functioning as molecular glue, Arbidol stabilizes the prefusion conformation of HA that inhibits the large conformational rearrangements associated with membrane fusion in the low pH of the endosome. This unique binding mode compared with the small-molecule inhibitors of other class I fusion proteins enhances our understanding of how small molecules can function as fusion inhibitors and guides the development of broad-spectrum therapeutics against influenza virus.
广谱抗病毒药物阿比朵尔通过作用于血凝素(HA)融合机制来对抗流感病毒。然而,阿比朵尔抑制融合的机制的结构基础仍不清楚,这阻碍了其作为一种特异性和优化的流感治疗药物的进一步开发。我们确定了阿比朵尔与1968年大流行的H3N2流感病毒和2013年的H7N9流感病毒的HA形成的复合物的晶体结构。阿比朵尔结合在HA三聚体茎部两个原体之间界面处的一个疏水腔内。这个腔位于广泛中和性茎抗体靶向的保守表位的远端,距离融合肽约16 Å。阿比朵尔主要与结合位点进行疏水相互作用,但也诱导一些构象重排以形成原体间和原体内盐桥网络。通过充当分子胶水,阿比朵尔稳定了HA的融合前构象,该构象抑制了在内体低pH值下与膜融合相关的大的构象重排。与其他I类融合蛋白的小分子抑制剂相比,这种独特的结合模式加深了我们对小分子如何作为融合抑制剂发挥作用的理解,并指导了针对流感病毒的广谱治疗药物的开发。