Serveur d'exploration H2N2

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Influenza Hemagglutinin and Neuraminidase Membrane Glycoproteins*

Identifieur interne : 000E63 ( Main/Exploration ); précédent : 000E62; suivant : 000E64

Influenza Hemagglutinin and Neuraminidase Membrane Glycoproteins*

Auteurs : Steven J. Gamblin [Royaume-Uni] ; John J. Skehel [Royaume-Uni]

Source :

RBID : PMC:2937864

Abstract

Considerable progress has been made toward understanding the structural basis of the interaction of the two major surface glycoproteins of influenza A virus with their common ligand/substrate: carbohydrate chains terminating in sialic acid. The specificity of virus attachment to target cells is mediated by hemagglutinin, which acquires characteristic changes in its receptor-binding site to switch its host from avian species to humans. Anti-influenza drugs mimic the natural sialic acid substrate of the virus neuraminidase enzyme but utilize the much tighter binding of the drugs for efficacy. Resistance to one of the two main antiviral drugs is differentially acquired by the two distinct subsets of neuraminidase as a consequence of structural differences in the enzyme active site between the two phylogenetic groups.


Url:
DOI: 10.1074/jbc.R110.129809
PubMed: 20538598
PubMed Central: 2937864


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Considerable progress has been made toward understanding the structural basis of the interaction of the two major surface glycoproteins of influenza A virus with their common ligand/substrate: carbohydrate chains terminating in sialic acid. The specificity of virus attachment to target cells is mediated by hemagglutinin, which acquires characteristic changes in its receptor-binding site to switch its host from avian species to humans. Anti-influenza drugs mimic the natural sialic acid substrate of the virus neuraminidase enzyme but utilize the much tighter binding of the drugs for efficacy. Resistance to one of the two main antiviral drugs is differentially acquired by the two distinct subsets of neuraminidase as a consequence of structural differences in the enzyme active site between the two phylogenetic groups.</p>
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