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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7551194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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