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Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin

[Image: see text] Membrane fusion is involved in many fundamental cellular processes and entry of enveloped viruses into host cells. Influenza type A virus HA has long served as a paradigm for mechanistic studies of protein-mediated membrane fusion via large-scale structural rearrangements induced b...

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Autores principales: Ni, Fengyun, Chen, Xiaorui, Shen, Jun, Wang, Qinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985705/
https://www.ncbi.nlm.nih.gov/pubmed/24433110
http://dx.doi.org/10.1021/bi401525h
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author Ni, Fengyun
Chen, Xiaorui
Shen, Jun
Wang, Qinghua
author_facet Ni, Fengyun
Chen, Xiaorui
Shen, Jun
Wang, Qinghua
author_sort Ni, Fengyun
collection PubMed
description [Image: see text] Membrane fusion is involved in many fundamental cellular processes and entry of enveloped viruses into host cells. Influenza type A virus HA has long served as a paradigm for mechanistic studies of protein-mediated membrane fusion via large-scale structural rearrangements induced by acidic pH. Here we report the newly determined crystal structure of influenza B virus HA(2) in the postfusion state. Together with a large number of previously determined prefusion structures of influenza A and B virus HA and a postfusion structure of influenza A/H3N2 HA(2), we identified conserved features that are shared between influenza A and B virus HA in the conformational transition and documented substantial differences that likely influence the detailed mechanisms of this process. Further studies are needed to dissect the effects of these and other structural differences in HA conformational changes and influenza pathogenicity and transmission, which may ultimately expedite the discovery of novel anti-influenza fusion inhibitors.
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spelling pubmed-39857052015-01-16 Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin Ni, Fengyun Chen, Xiaorui Shen, Jun Wang, Qinghua Biochemistry [Image: see text] Membrane fusion is involved in many fundamental cellular processes and entry of enveloped viruses into host cells. Influenza type A virus HA has long served as a paradigm for mechanistic studies of protein-mediated membrane fusion via large-scale structural rearrangements induced by acidic pH. Here we report the newly determined crystal structure of influenza B virus HA(2) in the postfusion state. Together with a large number of previously determined prefusion structures of influenza A and B virus HA and a postfusion structure of influenza A/H3N2 HA(2), we identified conserved features that are shared between influenza A and B virus HA in the conformational transition and documented substantial differences that likely influence the detailed mechanisms of this process. Further studies are needed to dissect the effects of these and other structural differences in HA conformational changes and influenza pathogenicity and transmission, which may ultimately expedite the discovery of novel anti-influenza fusion inhibitors. American Chemical Society 2014-01-16 2014-02-11 /pmc/articles/PMC3985705/ /pubmed/24433110 http://dx.doi.org/10.1021/bi401525h Text en Copyright © 2014 American Chemical Society
spellingShingle Ni, Fengyun
Chen, Xiaorui
Shen, Jun
Wang, Qinghua
Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
title Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
title_full Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
title_fullStr Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
title_full_unstemmed Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
title_short Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
title_sort structural insights into the membrane fusion mechanism mediated by influenza virus hemagglutinin
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985705/
https://www.ncbi.nlm.nih.gov/pubmed/24433110
http://dx.doi.org/10.1021/bi401525h
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