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Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins
Flaviviruses such as Dengue (DENV) or Zika virus (ZIKV) assemble into an immature form within the endoplasmatic reticulum (ER), and are then processed by furin protease in the trans-Golgi. To better grasp maturation, we carry out cryo-EM reconstructions of immature Spondweni virus (SPOV), a human fl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902656/ https://www.ncbi.nlm.nih.gov/pubmed/33623019 http://dx.doi.org/10.1038/s41467-021-21505-9 |
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author | Renner, Max Dejnirattisai, Wanwisa Carrique, Loïc Martin, Itziar Serna Karia, Dimple Ilca, Serban L. Ho, Shu F. Kotecha, Abhay Keown, Jeremy R. Mongkolsapaya, Juthathip Screaton, Gavin R. Grimes, Jonathan M. |
author_facet | Renner, Max Dejnirattisai, Wanwisa Carrique, Loïc Martin, Itziar Serna Karia, Dimple Ilca, Serban L. Ho, Shu F. Kotecha, Abhay Keown, Jeremy R. Mongkolsapaya, Juthathip Screaton, Gavin R. Grimes, Jonathan M. |
author_sort | Renner, Max |
collection | PubMed |
description | Flaviviruses such as Dengue (DENV) or Zika virus (ZIKV) assemble into an immature form within the endoplasmatic reticulum (ER), and are then processed by furin protease in the trans-Golgi. To better grasp maturation, we carry out cryo-EM reconstructions of immature Spondweni virus (SPOV), a human flavivirus of the same serogroup as ZIKV. By employing asymmetric localised reconstruction we push the resolution to 3.8 Å, enabling us to refine an atomic model which includes the crucial furin protease recognition site and a conserved Histidine pH-sensor. For direct comparison, we also solve structures of the mature forms of SPONV and DENV to 2.6 Å and 3.1 Å, respectively. We identify an ordered lipid that is present in only the mature forms of ZIKV, SPOV, and DENV and can bind as a consequence of rearranging amphipathic stem-helices of E during maturation. We propose a structural role for the pocket and suggest it stabilizes mature E. |
format | Online Article Text |
id | pubmed-7902656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79026562021-03-11 Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins Renner, Max Dejnirattisai, Wanwisa Carrique, Loïc Martin, Itziar Serna Karia, Dimple Ilca, Serban L. Ho, Shu F. Kotecha, Abhay Keown, Jeremy R. Mongkolsapaya, Juthathip Screaton, Gavin R. Grimes, Jonathan M. Nat Commun Article Flaviviruses such as Dengue (DENV) or Zika virus (ZIKV) assemble into an immature form within the endoplasmatic reticulum (ER), and are then processed by furin protease in the trans-Golgi. To better grasp maturation, we carry out cryo-EM reconstructions of immature Spondweni virus (SPOV), a human flavivirus of the same serogroup as ZIKV. By employing asymmetric localised reconstruction we push the resolution to 3.8 Å, enabling us to refine an atomic model which includes the crucial furin protease recognition site and a conserved Histidine pH-sensor. For direct comparison, we also solve structures of the mature forms of SPONV and DENV to 2.6 Å and 3.1 Å, respectively. We identify an ordered lipid that is present in only the mature forms of ZIKV, SPOV, and DENV and can bind as a consequence of rearranging amphipathic stem-helices of E during maturation. We propose a structural role for the pocket and suggest it stabilizes mature E. Nature Publishing Group UK 2021-02-23 /pmc/articles/PMC7902656/ /pubmed/33623019 http://dx.doi.org/10.1038/s41467-021-21505-9 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Renner, Max Dejnirattisai, Wanwisa Carrique, Loïc Martin, Itziar Serna Karia, Dimple Ilca, Serban L. Ho, Shu F. Kotecha, Abhay Keown, Jeremy R. Mongkolsapaya, Juthathip Screaton, Gavin R. Grimes, Jonathan M. Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
title | Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
title_full | Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
title_fullStr | Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
title_full_unstemmed | Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
title_short | Flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
title_sort | flavivirus maturation leads to the formation of an occupied lipid pocket in the surface glycoproteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902656/ https://www.ncbi.nlm.nih.gov/pubmed/33623019 http://dx.doi.org/10.1038/s41467-021-21505-9 |
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