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A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71
Enterovirus 71 (EV71), a major agent of hand-foot-and-mouth disease in children, can cause severe central nervous system disease and mortality. At present no vaccine or antiviral therapy is available. We have determined high-resolution structures for the mature virus and natural empty particles. The...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378640/ https://www.ncbi.nlm.nih.gov/pubmed/22388738 http://dx.doi.org/10.1038/nsmb.2255 |
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author | Wang, Xiangxi Peng, Wei Ren, Jingshan Hu, Zhongyu Xu, Jiwei Lou, Zhiyong Li, Xumei Yin, Weidong Shen, Xinliang Porta, Claudine Walter, Thomas S. Evans, Gwyndaf Axford, Danny Owen, Robin Rowlands, David J. Wang, Junzhi Stuart, David I. Fry, Elizabeth E. Rao, Zihe |
author_facet | Wang, Xiangxi Peng, Wei Ren, Jingshan Hu, Zhongyu Xu, Jiwei Lou, Zhiyong Li, Xumei Yin, Weidong Shen, Xinliang Porta, Claudine Walter, Thomas S. Evans, Gwyndaf Axford, Danny Owen, Robin Rowlands, David J. Wang, Junzhi Stuart, David I. Fry, Elizabeth E. Rao, Zihe |
author_sort | Wang, Xiangxi |
collection | PubMed |
description | Enterovirus 71 (EV71), a major agent of hand-foot-and-mouth disease in children, can cause severe central nervous system disease and mortality. At present no vaccine or antiviral therapy is available. We have determined high-resolution structures for the mature virus and natural empty particles. The structure of the mature virus is similar to that of other enteroviruses, whilst the empty particles are dramatically expanded, with notable fissures, resembling elusive enterovirus uncoating intermediates not previously characterized in atomic detail. Hydrophobic capsid pockets within the EV71 capsid are collapsed in this expanded particle, providing a detailed explanation of the mechanism for receptor-binding triggered virus uncoating. The results provide a paradigm for enterovirus uncoating, in which the VP1 GH loop acts as an adaptor-sensor for the attachment of cellular receptors, converting heterologous inputs to a generic uncoating mechanism, spotlighting novel points for therapeutic intervention. |
format | Online Article Text |
id | pubmed-3378640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-33786402012-10-01 A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 Wang, Xiangxi Peng, Wei Ren, Jingshan Hu, Zhongyu Xu, Jiwei Lou, Zhiyong Li, Xumei Yin, Weidong Shen, Xinliang Porta, Claudine Walter, Thomas S. Evans, Gwyndaf Axford, Danny Owen, Robin Rowlands, David J. Wang, Junzhi Stuart, David I. Fry, Elizabeth E. Rao, Zihe Nat Struct Mol Biol Article Enterovirus 71 (EV71), a major agent of hand-foot-and-mouth disease in children, can cause severe central nervous system disease and mortality. At present no vaccine or antiviral therapy is available. We have determined high-resolution structures for the mature virus and natural empty particles. The structure of the mature virus is similar to that of other enteroviruses, whilst the empty particles are dramatically expanded, with notable fissures, resembling elusive enterovirus uncoating intermediates not previously characterized in atomic detail. Hydrophobic capsid pockets within the EV71 capsid are collapsed in this expanded particle, providing a detailed explanation of the mechanism for receptor-binding triggered virus uncoating. The results provide a paradigm for enterovirus uncoating, in which the VP1 GH loop acts as an adaptor-sensor for the attachment of cellular receptors, converting heterologous inputs to a generic uncoating mechanism, spotlighting novel points for therapeutic intervention. 2012-03-04 /pmc/articles/PMC3378640/ /pubmed/22388738 http://dx.doi.org/10.1038/nsmb.2255 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Wang, Xiangxi Peng, Wei Ren, Jingshan Hu, Zhongyu Xu, Jiwei Lou, Zhiyong Li, Xumei Yin, Weidong Shen, Xinliang Porta, Claudine Walter, Thomas S. Evans, Gwyndaf Axford, Danny Owen, Robin Rowlands, David J. Wang, Junzhi Stuart, David I. Fry, Elizabeth E. Rao, Zihe A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 |
title | A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 |
title_full | A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 |
title_fullStr | A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 |
title_full_unstemmed | A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 |
title_short | A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71 |
title_sort | sensor-adaptor mechanism for enterovirus uncoating from structures of ev71 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378640/ https://www.ncbi.nlm.nih.gov/pubmed/22388738 http://dx.doi.org/10.1038/nsmb.2255 |
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