Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783654573136674816
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
work_keys_str_mv AT rennermax flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT dejnirattisaiwanwisa flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT carriqueloic flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT martinitziarserna flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT kariadimple flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT ilcaserbanl flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT hoshuf flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT kotechaabhay flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT keownjeremyr flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT mongkolsapayajuthathip flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT screatongavinr flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins
AT grimesjonathanm flavivirusmaturationleadstotheformationofanoccupiedlipidpocketinthesurfaceglycoproteins