Literature DB >> 14764886

The structure and receptor binding properties of the 1918 influenza hemagglutinin.

S J Gamblin1, L F Haire, R J Russell, D J Stevens, B Xiao, Y Ha, N Vasisht, D A Steinhauer, R S Daniels, A Elliot, D C Wiley, J J Skehel.   

Abstract

The 1918 influenza pandemic resulted in about 20 million deaths. This enormous impact, coupled with renewed interest in emerging infections, makes characterization of the virus involved a priority. Receptor binding, the initial event in virus infection, is a major determinant of virus transmissibility that, for influenza viruses, is mediated by the hemagglutinin (HA) membrane glycoprotein. We have determined the crystal structures of the HA from the 1918 virus and two closely related HAs in complex with receptor analogs. They explain how the 1918 HA, while retaining receptor binding site amino acids characteristic of an avian precursor HA, is able to bind human receptors and how, as a consequence, the virus was able to spread in the human population.

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Year:  2004        PMID: 14764886     DOI: 10.1126/science.1093155

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  279 in total

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9.  A human-infecting H10N8 influenza virus retains a strong preference for avian-type receptors.

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