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Structural insight into Marburg virus nucleoprotein–RNA complex formation
The nucleoprotein (NP) of Marburg virus (MARV), a close relative of Ebola virus (EBOV), encapsidates the single-stranded, negative-sense viral genomic RNA (vRNA) to form the helical NP–RNA complex. The NP–RNA complex constitutes the core structure for the assembly of the nucleocapsid that is respons...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897395/ https://www.ncbi.nlm.nih.gov/pubmed/35246537 http://dx.doi.org/10.1038/s41467-022-28802-x |
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author | Fujita-Fujiharu, Yoko Sugita, Yukihiko Takamatsu, Yuki Houri, Kazuya Igarashi, Manabu Muramoto, Yukiko Nakano, Masahiro Tsunoda, Yugo Taniguchi, Ichiro Becker, Stephan Noda, Takeshi |
author_facet | Fujita-Fujiharu, Yoko Sugita, Yukihiko Takamatsu, Yuki Houri, Kazuya Igarashi, Manabu Muramoto, Yukiko Nakano, Masahiro Tsunoda, Yugo Taniguchi, Ichiro Becker, Stephan Noda, Takeshi |
author_sort | Fujita-Fujiharu, Yoko |
collection | PubMed |
description | The nucleoprotein (NP) of Marburg virus (MARV), a close relative of Ebola virus (EBOV), encapsidates the single-stranded, negative-sense viral genomic RNA (vRNA) to form the helical NP–RNA complex. The NP–RNA complex constitutes the core structure for the assembly of the nucleocapsid that is responsible for viral RNA synthesis. Although appropriate interactions among NPs and RNA are required for the formation of nucleocapsid, the structural basis of the helical assembly remains largely elusive. Here, we show the structure of the MARV NP–RNA complex determined using cryo-electron microscopy at a resolution of 3.1 Å. The structures of the asymmetric unit, a complex of an NP and six RNA nucleotides, was very similar to that of EBOV, suggesting that both viruses share common mechanisms for the nucleocapsid formation. Structure-based mutational analysis of both MARV and EBOV NPs identified key residues for helical assembly and subsequent viral RNA synthesis. Importantly, most of the residues identified were conserved in both viruses. These findings provide a structural basis for understanding the nucleocapsid formation and contribute to the development of novel antivirals against MARV and EBOV. |
format | Online Article Text |
id | pubmed-8897395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88973952022-03-17 Structural insight into Marburg virus nucleoprotein–RNA complex formation Fujita-Fujiharu, Yoko Sugita, Yukihiko Takamatsu, Yuki Houri, Kazuya Igarashi, Manabu Muramoto, Yukiko Nakano, Masahiro Tsunoda, Yugo Taniguchi, Ichiro Becker, Stephan Noda, Takeshi Nat Commun Article The nucleoprotein (NP) of Marburg virus (MARV), a close relative of Ebola virus (EBOV), encapsidates the single-stranded, negative-sense viral genomic RNA (vRNA) to form the helical NP–RNA complex. The NP–RNA complex constitutes the core structure for the assembly of the nucleocapsid that is responsible for viral RNA synthesis. Although appropriate interactions among NPs and RNA are required for the formation of nucleocapsid, the structural basis of the helical assembly remains largely elusive. Here, we show the structure of the MARV NP–RNA complex determined using cryo-electron microscopy at a resolution of 3.1 Å. The structures of the asymmetric unit, a complex of an NP and six RNA nucleotides, was very similar to that of EBOV, suggesting that both viruses share common mechanisms for the nucleocapsid formation. Structure-based mutational analysis of both MARV and EBOV NPs identified key residues for helical assembly and subsequent viral RNA synthesis. Importantly, most of the residues identified were conserved in both viruses. These findings provide a structural basis for understanding the nucleocapsid formation and contribute to the development of novel antivirals against MARV and EBOV. Nature Publishing Group UK 2022-03-04 /pmc/articles/PMC8897395/ /pubmed/35246537 http://dx.doi.org/10.1038/s41467-022-28802-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fujita-Fujiharu, Yoko Sugita, Yukihiko Takamatsu, Yuki Houri, Kazuya Igarashi, Manabu Muramoto, Yukiko Nakano, Masahiro Tsunoda, Yugo Taniguchi, Ichiro Becker, Stephan Noda, Takeshi Structural insight into Marburg virus nucleoprotein–RNA complex formation |
title | Structural insight into Marburg virus nucleoprotein–RNA complex formation |
title_full | Structural insight into Marburg virus nucleoprotein–RNA complex formation |
title_fullStr | Structural insight into Marburg virus nucleoprotein–RNA complex formation |
title_full_unstemmed | Structural insight into Marburg virus nucleoprotein–RNA complex formation |
title_short | Structural insight into Marburg virus nucleoprotein–RNA complex formation |
title_sort | structural insight into marburg virus nucleoprotein–rna complex formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897395/ https://www.ncbi.nlm.nih.gov/pubmed/35246537 http://dx.doi.org/10.1038/s41467-022-28802-x |
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