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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...

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Autores principales: Banadyga, Logan, Hoenen, Thomas, Ambroggio, Xavier, Dunham, Eric, Groseth, Allison, Ebihara, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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