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Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging
Ebola virus causes devastating hemorrhagic fever outbreaks for which no approved therapeutic exists. The viral nucleocapsid, which is minimally composed of the proteins NP, VP35, and VP24, represents an attractive target for drug development; however, the molecular determinants that govern the inter...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550494/ https://www.ncbi.nlm.nih.gov/pubmed/28794491 http://dx.doi.org/10.1038/s41598-017-08167-8 |
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author | Banadyga, Logan Hoenen, Thomas Ambroggio, Xavier Dunham, Eric Groseth, Allison Ebihara, Hideki |
author_facet | Banadyga, Logan Hoenen, Thomas Ambroggio, Xavier Dunham, Eric Groseth, Allison Ebihara, Hideki |
author_sort | Banadyga, Logan |
collection | PubMed |
description | Ebola virus causes devastating hemorrhagic fever outbreaks for which no approved therapeutic exists. The viral nucleocapsid, which is minimally composed of the proteins NP, VP35, and VP24, represents an attractive target for drug development; however, the molecular determinants that govern the interactions and functions of these three proteins are still unknown. Through a series of mutational analyses, in combination with biochemical and bioinformatics approaches, we identified a region on VP24 that was critical for its interaction with NP. Importantly, we demonstrated that the interaction between VP24 and NP was required for both nucleocapsid assembly and genome packaging. Not only does this study underscore the critical role that these proteins play in the viral replication cycle, but it also identifies a key interaction interface on VP24 that may serve as a novel target for antiviral therapeutic intervention. |
format | Online Article Text |
id | pubmed-5550494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55504942017-08-11 Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging Banadyga, Logan Hoenen, Thomas Ambroggio, Xavier Dunham, Eric Groseth, Allison Ebihara, Hideki Sci Rep Article Ebola virus causes devastating hemorrhagic fever outbreaks for which no approved therapeutic exists. The viral nucleocapsid, which is minimally composed of the proteins NP, VP35, and VP24, represents an attractive target for drug development; however, the molecular determinants that govern the interactions and functions of these three proteins are still unknown. Through a series of mutational analyses, in combination with biochemical and bioinformatics approaches, we identified a region on VP24 that was critical for its interaction with NP. Importantly, we demonstrated that the interaction between VP24 and NP was required for both nucleocapsid assembly and genome packaging. Not only does this study underscore the critical role that these proteins play in the viral replication cycle, but it also identifies a key interaction interface on VP24 that may serve as a novel target for antiviral therapeutic intervention. Nature Publishing Group UK 2017-08-09 /pmc/articles/PMC5550494/ /pubmed/28794491 http://dx.doi.org/10.1038/s41598-017-08167-8 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Banadyga, Logan Hoenen, Thomas Ambroggio, Xavier Dunham, Eric Groseth, Allison Ebihara, Hideki Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging |
title | Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging |
title_full | Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging |
title_fullStr | Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging |
title_full_unstemmed | Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging |
title_short | Ebola virus VP24 interacts with NP to facilitate nucleocapsid assembly and genome packaging |
title_sort | ebola virus vp24 interacts with np to facilitate nucleocapsid assembly and genome packaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550494/ https://www.ncbi.nlm.nih.gov/pubmed/28794491 http://dx.doi.org/10.1038/s41598-017-08167-8 |
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