Journal of Virology · 2018 · 50 citations · 66 references
Life SciencesInfectious DiseasesMolecular BiologyMolecular VirologyStructural BiologyVirologyAmino Acid PropertiesAmino Acid Sequence DeterminantsAmino Acid StructureProtein StructureViral VaccinesVirus StructureAmino AcidsAvian Influenza VirusAvian Influenza VirusesHemagglutinin-receptor BindingRational Vaccine DesignReceptor Binding SpecificityStructural Basis Of Receptor RecognitionViral Receptor Usage
A single amino acid change at position 226 in the hemagglutinin (HA) from glutamine (Q) to leucine (L) has been shown to play a key role in receptor specificity switching in various influenza virus HA subtypes, including H9. We tested the flexibility of amino acid usage and determined the effects of such changes. The results reveal that amino acids other than L226 and Q226 are well tolerated and that some amino acids allow for the recognition of both avian and human influenza virus receptors in the absence of other changes. Our results can inform better avian influenza virus surveillance efforts as well as contribute to rational vaccine design and improve structural molecular dynamics algorithms.
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