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Structural Studies of the Giant Mimivirus
Mimivirus is the largest known virus whose genome and physical size are comparable to some small bacteria, blurring the boundary between a virus and a cell. Structural studies of Mimivirus have been difficult because of its size and long surface fibers. Here we report the use of enzymatic digestions...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671561/ https://www.ncbi.nlm.nih.gov/pubmed/19402750 http://dx.doi.org/10.1371/journal.pbio.1000092 |
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author | Xiao, Chuan Kuznetsov, Yurii G Sun, Siyang Hafenstein, Susan L Kostyuchenko, Victor A Chipman, Paul R Suzan-Monti, Marie Raoult, Didier McPherson, Alexander Rossmann, Michael G |
author_facet | Xiao, Chuan Kuznetsov, Yurii G Sun, Siyang Hafenstein, Susan L Kostyuchenko, Victor A Chipman, Paul R Suzan-Monti, Marie Raoult, Didier McPherson, Alexander Rossmann, Michael G |
author_sort | Xiao, Chuan |
collection | PubMed |
description | Mimivirus is the largest known virus whose genome and physical size are comparable to some small bacteria, blurring the boundary between a virus and a cell. Structural studies of Mimivirus have been difficult because of its size and long surface fibers. Here we report the use of enzymatic digestions to remove the surface fibers of Mimivirus in order to expose the surface of the viral capsid. Cryo-electron microscopy (cryoEM) and atomic force microscopy were able to show that the 20 icosahedral faces of Mimivirus capsids have hexagonal arrays of depressions. Each depression is surrounded by six trimeric capsomers that are similar in structure to those in many other large, icosahedral double-stranded DNA viruses. Whereas in most viruses these capsomers are hexagonally close-packed with the same orientation in each face, in Mimivirus there are vacancies at the systematic depressions with neighboring capsomers differing in orientation by 60°. The previously observed starfish-shaped feature is well-resolved and found to be on each virus particle and is associated with a special pentameric vertex. The arms of the starfish fit into the gaps between the five faces surrounding the unique vertex, acting as a seal. Furthermore, the enveloped nucleocapsid is accurately positioned and oriented within the capsid with a concave surface facing the unique vertex. Thus, the starfish-shaped feature and the organization of the nucleocapsid might regulate the delivery of the genome to the host. The structure of Mimivirus, as well as the various fiber components observed in the virus, suggests that the Mimivirus genome includes genes derived from both eukaryotic and prokaryotic organisms. The three-dimensional cryoEM reconstruction reported here is of a virus with a volume that is one order of magnitude larger than any previously reported molecular assembly studied at a resolution of equal to or better than 65 Å. |
format | Text |
id | pubmed-2671561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26715612009-04-28 Structural Studies of the Giant Mimivirus Xiao, Chuan Kuznetsov, Yurii G Sun, Siyang Hafenstein, Susan L Kostyuchenko, Victor A Chipman, Paul R Suzan-Monti, Marie Raoult, Didier McPherson, Alexander Rossmann, Michael G PLoS Biol Research Article Mimivirus is the largest known virus whose genome and physical size are comparable to some small bacteria, blurring the boundary between a virus and a cell. Structural studies of Mimivirus have been difficult because of its size and long surface fibers. Here we report the use of enzymatic digestions to remove the surface fibers of Mimivirus in order to expose the surface of the viral capsid. Cryo-electron microscopy (cryoEM) and atomic force microscopy were able to show that the 20 icosahedral faces of Mimivirus capsids have hexagonal arrays of depressions. Each depression is surrounded by six trimeric capsomers that are similar in structure to those in many other large, icosahedral double-stranded DNA viruses. Whereas in most viruses these capsomers are hexagonally close-packed with the same orientation in each face, in Mimivirus there are vacancies at the systematic depressions with neighboring capsomers differing in orientation by 60°. The previously observed starfish-shaped feature is well-resolved and found to be on each virus particle and is associated with a special pentameric vertex. The arms of the starfish fit into the gaps between the five faces surrounding the unique vertex, acting as a seal. Furthermore, the enveloped nucleocapsid is accurately positioned and oriented within the capsid with a concave surface facing the unique vertex. Thus, the starfish-shaped feature and the organization of the nucleocapsid might regulate the delivery of the genome to the host. The structure of Mimivirus, as well as the various fiber components observed in the virus, suggests that the Mimivirus genome includes genes derived from both eukaryotic and prokaryotic organisms. The three-dimensional cryoEM reconstruction reported here is of a virus with a volume that is one order of magnitude larger than any previously reported molecular assembly studied at a resolution of equal to or better than 65 Å. Public Library of Science 2009-04 2009-04-28 /pmc/articles/PMC2671561/ /pubmed/19402750 http://dx.doi.org/10.1371/journal.pbio.1000092 Text en © 2009 Xiao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Xiao, Chuan Kuznetsov, Yurii G Sun, Siyang Hafenstein, Susan L Kostyuchenko, Victor A Chipman, Paul R Suzan-Monti, Marie Raoult, Didier McPherson, Alexander Rossmann, Michael G Structural Studies of the Giant Mimivirus |
title | Structural Studies of the Giant Mimivirus |
title_full | Structural Studies of the Giant Mimivirus |
title_fullStr | Structural Studies of the Giant Mimivirus |
title_full_unstemmed | Structural Studies of the Giant Mimivirus |
title_short | Structural Studies of the Giant Mimivirus |
title_sort | structural studies of the giant mimivirus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671561/ https://www.ncbi.nlm.nih.gov/pubmed/19402750 http://dx.doi.org/10.1371/journal.pbio.1000092 |
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