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4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus
Venezuelan equine encephalitis virus (VEEV), a member of the membrane-containing Alphavirus genus, is a human and equine pathogen, and has been developed as a biological weapon. Using electron cryo-microscopy (cryo-EM), we determined the structure of an attenuated vaccine strain, TC-83, of VEEV to 4...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173789/ https://www.ncbi.nlm.nih.gov/pubmed/21829169 http://dx.doi.org/10.1038/emboj.2011.261 |
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author | Zhang, Rui Hryc, Corey F Cong, Yao Liu, Xiangan Jakana, Joanita Gorchakov, Rodion Baker, Matthew L Weaver, Scott C Chiu, Wah |
author_facet | Zhang, Rui Hryc, Corey F Cong, Yao Liu, Xiangan Jakana, Joanita Gorchakov, Rodion Baker, Matthew L Weaver, Scott C Chiu, Wah |
author_sort | Zhang, Rui |
collection | PubMed |
description | Venezuelan equine encephalitis virus (VEEV), a member of the membrane-containing Alphavirus genus, is a human and equine pathogen, and has been developed as a biological weapon. Using electron cryo-microscopy (cryo-EM), we determined the structure of an attenuated vaccine strain, TC-83, of VEEV to 4.4 Å resolution. Our density map clearly resolves regions (including E1, E2 transmembrane helices and cytoplasmic tails) that were missing in the crystal structures of domains of alphavirus subunits. These new features are implicated in the fusion, assembly and budding processes of alphaviruses. Furthermore, our map reveals the unexpected E3 protein, which is cleaved and generally thought to be absent in the mature VEEV. Our structural results suggest a mechanism for the initial stage of nucleocapsid core formation, and shed light on the virulence attenuation, host recognition and neutralizing activities of VEEV and other alphavirus pathogens. |
format | Online Article Text |
id | pubmed-3173789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-31737892011-10-21 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus Zhang, Rui Hryc, Corey F Cong, Yao Liu, Xiangan Jakana, Joanita Gorchakov, Rodion Baker, Matthew L Weaver, Scott C Chiu, Wah EMBO J Article Venezuelan equine encephalitis virus (VEEV), a member of the membrane-containing Alphavirus genus, is a human and equine pathogen, and has been developed as a biological weapon. Using electron cryo-microscopy (cryo-EM), we determined the structure of an attenuated vaccine strain, TC-83, of VEEV to 4.4 Å resolution. Our density map clearly resolves regions (including E1, E2 transmembrane helices and cytoplasmic tails) that were missing in the crystal structures of domains of alphavirus subunits. These new features are implicated in the fusion, assembly and budding processes of alphaviruses. Furthermore, our map reveals the unexpected E3 protein, which is cleaved and generally thought to be absent in the mature VEEV. Our structural results suggest a mechanism for the initial stage of nucleocapsid core formation, and shed light on the virulence attenuation, host recognition and neutralizing activities of VEEV and other alphavirus pathogens. European Molecular Biology Organization 2011-09-14 2011-08-09 /pmc/articles/PMC3173789/ /pubmed/21829169 http://dx.doi.org/10.1038/emboj.2011.261 Text en Copyright © 2011, European Molecular Biology Organization https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission. |
spellingShingle | Article Zhang, Rui Hryc, Corey F Cong, Yao Liu, Xiangan Jakana, Joanita Gorchakov, Rodion Baker, Matthew L Weaver, Scott C Chiu, Wah 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus |
title | 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus |
title_full | 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus |
title_fullStr | 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus |
title_full_unstemmed | 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus |
title_short | 4.4 Å cryo-EM structure of an enveloped alphavirus Venezuelan equine encephalitis virus |
title_sort | 4.4 å cryo-em structure of an enveloped alphavirus venezuelan equine encephalitis virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173789/ https://www.ncbi.nlm.nih.gov/pubmed/21829169 http://dx.doi.org/10.1038/emboj.2011.261 |
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