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Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure

Hemagglutinin (HA) glycoprotein is an important focus of influenza research due to its role in antigenic drift and shift, as well as its receptor binding and membrane fusion functions, which are indispensable for viral entry. Over the past four decades, X-ray crystallography has greatly facilitated...

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Autores principales: Wu, Nicholas C., Wilson, Ian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551194/
https://www.ncbi.nlm.nih.gov/pubmed/32971825
http://dx.doi.org/10.3390/v12091053
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author Wu, Nicholas C.
Wilson, Ian A.
author_facet Wu, Nicholas C.
Wilson, Ian A.
author_sort Wu, Nicholas C.
collection PubMed
description Hemagglutinin (HA) glycoprotein is an important focus of influenza research due to its role in antigenic drift and shift, as well as its receptor binding and membrane fusion functions, which are indispensable for viral entry. Over the past four decades, X-ray crystallography has greatly facilitated our understanding of HA receptor binding, membrane fusion, and antigenicity. The recent advances in cryo-EM have further deepened our comprehension of HA biology. Since influenza HA constantly evolves in natural circulating strains, there are always new questions to be answered. The incessant accumulation of knowledge on the structural biology of HA over several decades has also facilitated the design and development of novel therapeutics and vaccines. This review describes the current status of the field of HA structural biology, how we got here, and what the next steps might be.
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spelling pubmed-75511942020-10-16 Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure Wu, Nicholas C. Wilson, Ian A. Viruses Review Hemagglutinin (HA) glycoprotein is an important focus of influenza research due to its role in antigenic drift and shift, as well as its receptor binding and membrane fusion functions, which are indispensable for viral entry. Over the past four decades, X-ray crystallography has greatly facilitated our understanding of HA receptor binding, membrane fusion, and antigenicity. The recent advances in cryo-EM have further deepened our comprehension of HA biology. Since influenza HA constantly evolves in natural circulating strains, there are always new questions to be answered. The incessant accumulation of knowledge on the structural biology of HA over several decades has also facilitated the design and development of novel therapeutics and vaccines. This review describes the current status of the field of HA structural biology, how we got here, and what the next steps might be. MDPI 2020-09-22 /pmc/articles/PMC7551194/ /pubmed/32971825 http://dx.doi.org/10.3390/v12091053 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wu, Nicholas C.
Wilson, Ian A.
Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure
title Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure
title_full Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure
title_fullStr Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure
title_full_unstemmed Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure
title_short Structural Biology of Influenza Hemagglutinin: An Amaranthine Adventure
title_sort structural biology of influenza hemagglutinin: an amaranthine adventure
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551194/
https://www.ncbi.nlm.nih.gov/pubmed/32971825
http://dx.doi.org/10.3390/v12091053
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