A sensor-adaptor mechanism for enterovirus uncoating from structures of EV71
Enterovirus 71 (EV71) is a major agent of hand, foot and mouth disease in children, but no vaccine or antiviral therapy is available. Structural analysis of the mature virus and natural empty particles reveals that the larger empty particles resemble elusive enterovirus uncoating intermediates, allo...
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Published in | Nature structural & molecular biology Vol. 19; no. 4; pp. 424 - 429 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.04.2012
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1545-9993 1545-9985 1545-9985 |
DOI | 10.1038/nsmb.2255 |
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Summary: | Enterovirus 71 (EV71) is a major agent of hand, foot and mouth disease in children, but no vaccine or antiviral therapy is available. Structural analysis of the mature virus and natural empty particles reveals that the larger empty particles resemble elusive enterovirus uncoating intermediates, allowing insight into the process of enterovirus uncoating.
Enterovirus 71 (EV71) is a major agent of hand, foot and mouth disease in children that can cause severe central nervous system disease and death. No vaccine or antiviral therapy is available. High-resolution structural analysis of the mature virus and natural empty particles shows that the mature virus is structurally similar to other enteroviruses. In contrast, the empty particles are markedly expanded and resemble elusive enterovirus-uncoating intermediates not previously characterized in atomic detail. Hydrophobic pockets in the EV71 capsid are collapsed in this expanded particle, providing a detailed explanation of the mechanism for receptor-binding triggered virus uncoating. These structures provide a model for enterovirus uncoating in which the VP1 GH loop acts as an adaptor-sensor for cellular receptor attachment, converting heterologous inputs to a generic uncoating mechanism, highlighting new opportunities for therapeutic intervention. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 X.W., W.P. and J.R. contributed equally to this work. Author Contribution. JW, ZH, WY and XS prepared samples. XW, WP, XL, ZL, JX,JR, CP, TSW, EEF and DIS performed research, WP, XW, ZL JR, EEF and DIS analysed data and with DJR and ZR wrote the manuscript, in discussion with JW, ZH, WY and XS. All authors contributed to experimental design. Project supervision: ZR, DIS. |
ISSN: | 1545-9993 1545-9985 1545-9985 |
DOI: | 10.1038/nsmb.2255 |