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pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin

Influenza hemagglutinin (HA) is a viral membrane bound protein that plays a critical role in the viral life cycle by mediating entry into target cells. HA exploits the lowering of the pH in the endosomal compartment to initiate a series of conformational changes that promote access of the viral gene...

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Detalles Bibliográficos
Autores principales: Caffrey, Michael, Lavie, Arnon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718792/
https://www.ncbi.nlm.nih.gov/pubmed/34977156
http://dx.doi.org/10.3389/fmolb.2021.777095
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author Caffrey, Michael
Lavie, Arnon
author_facet Caffrey, Michael
Lavie, Arnon
author_sort Caffrey, Michael
collection PubMed
description Influenza hemagglutinin (HA) is a viral membrane bound protein that plays a critical role in the viral life cycle by mediating entry into target cells. HA exploits the lowering of the pH in the endosomal compartment to initiate a series of conformational changes that promote access of the viral genetic material to the cytoplasm, and hence viral replication. In this review we will first discuss what is known about the structural properties of HA as a function of pH. Next, we will discuss the dynamics and intermediate states of HA. We will then discuss the specific residues that are thought to be titrated by the change in pH and possible mechanisms for the pH triggered conformational changes. Finally, we will discuss small molecules that disrupt the pH trigger and thus serve as potential therapeutic strategies to prevent influenza infection.
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spelling pubmed-87187922022-01-01 pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin Caffrey, Michael Lavie, Arnon Front Mol Biosci Molecular Biosciences Influenza hemagglutinin (HA) is a viral membrane bound protein that plays a critical role in the viral life cycle by mediating entry into target cells. HA exploits the lowering of the pH in the endosomal compartment to initiate a series of conformational changes that promote access of the viral genetic material to the cytoplasm, and hence viral replication. In this review we will first discuss what is known about the structural properties of HA as a function of pH. Next, we will discuss the dynamics and intermediate states of HA. We will then discuss the specific residues that are thought to be titrated by the change in pH and possible mechanisms for the pH triggered conformational changes. Finally, we will discuss small molecules that disrupt the pH trigger and thus serve as potential therapeutic strategies to prevent influenza infection. Frontiers Media S.A. 2021-12-17 /pmc/articles/PMC8718792/ /pubmed/34977156 http://dx.doi.org/10.3389/fmolb.2021.777095 Text en Copyright © 2021 Caffrey and Lavie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Caffrey, Michael
Lavie, Arnon
pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin
title pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin
title_full pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin
title_fullStr pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin
title_full_unstemmed pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin
title_short pH-Dependent Mechanisms of Influenza Infection Mediated by Hemagglutinin
title_sort ph-dependent mechanisms of influenza infection mediated by hemagglutinin
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718792/
https://www.ncbi.nlm.nih.gov/pubmed/34977156
http://dx.doi.org/10.3389/fmolb.2021.777095
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