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A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses
The epidemic emergence of relatively rare and geographically isolated flaviviruses adds to the ongoing disease burden of viruses such as dengue. Structural analysis is key to understand and combat these pathogens. Here, we present a chimeric platform based on an insect-specific flavivirus for the sa...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169900/ https://www.ncbi.nlm.nih.gov/pubmed/34075032 http://dx.doi.org/10.1038/s41467-021-22773-1 |
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author | Hardy, Joshua M. Newton, Natalee D. Modhiran, Naphak Scott, Connor A. P. Venugopal, Hariprasad Vet, Laura J. Young, Paul R. Hall, Roy A. Hobson-Peters, Jody Coulibaly, Fasséli Watterson, Daniel |
author_facet | Hardy, Joshua M. Newton, Natalee D. Modhiran, Naphak Scott, Connor A. P. Venugopal, Hariprasad Vet, Laura J. Young, Paul R. Hall, Roy A. Hobson-Peters, Jody Coulibaly, Fasséli Watterson, Daniel |
author_sort | Hardy, Joshua M. |
collection | PubMed |
description | The epidemic emergence of relatively rare and geographically isolated flaviviruses adds to the ongoing disease burden of viruses such as dengue. Structural analysis is key to understand and combat these pathogens. Here, we present a chimeric platform based on an insect-specific flavivirus for the safe and rapid structural analysis of pathogenic viruses. We use this approach to resolve the architecture of two neurotropic viruses and a structure of dengue virus at 2.5 Å, the highest resolution for an enveloped virion. These reconstructions allow improved modelling of the stem region of the envelope protein, revealing two lipid-like ligands within highly conserved pockets. We show that these sites are essential for viral growth and important for viral maturation. These findings define a hallmark of flavivirus virions and a potential target for broad-spectrum antivirals and vaccine design. We anticipate the chimeric platform to be widely applicable for investigating flavivirus biology. |
format | Online Article Text |
id | pubmed-8169900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81699002021-06-07 A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses Hardy, Joshua M. Newton, Natalee D. Modhiran, Naphak Scott, Connor A. P. Venugopal, Hariprasad Vet, Laura J. Young, Paul R. Hall, Roy A. Hobson-Peters, Jody Coulibaly, Fasséli Watterson, Daniel Nat Commun Article The epidemic emergence of relatively rare and geographically isolated flaviviruses adds to the ongoing disease burden of viruses such as dengue. Structural analysis is key to understand and combat these pathogens. Here, we present a chimeric platform based on an insect-specific flavivirus for the safe and rapid structural analysis of pathogenic viruses. We use this approach to resolve the architecture of two neurotropic viruses and a structure of dengue virus at 2.5 Å, the highest resolution for an enveloped virion. These reconstructions allow improved modelling of the stem region of the envelope protein, revealing two lipid-like ligands within highly conserved pockets. We show that these sites are essential for viral growth and important for viral maturation. These findings define a hallmark of flavivirus virions and a potential target for broad-spectrum antivirals and vaccine design. We anticipate the chimeric platform to be widely applicable for investigating flavivirus biology. Nature Publishing Group UK 2021-06-01 /pmc/articles/PMC8169900/ /pubmed/34075032 http://dx.doi.org/10.1038/s41467-021-22773-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hardy, Joshua M. Newton, Natalee D. Modhiran, Naphak Scott, Connor A. P. Venugopal, Hariprasad Vet, Laura J. Young, Paul R. Hall, Roy A. Hobson-Peters, Jody Coulibaly, Fasséli Watterson, Daniel A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
title | A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
title_full | A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
title_fullStr | A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
title_full_unstemmed | A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
title_short | A unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
title_sort | unified route for flavivirus structures uncovers essential pocket factors conserved across pathogenic viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169900/ https://www.ncbi.nlm.nih.gov/pubmed/34075032 http://dx.doi.org/10.1038/s41467-021-22773-1 |
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