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Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network
COPII mediates Endoplasmic Reticulum to Golgi trafficking of thousands of cargoes. Five essential proteins assemble into a two-layer architecture, with the inner layer thought to regulate coat assembly and cargo recruitment, and the outer coat forming cages assumed to scaffold membrane curvature. He...
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/PMC8016994/ https://www.ncbi.nlm.nih.gov/pubmed/33795673 http://dx.doi.org/10.1038/s41467-021-22110-6 |
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author | Hutchings, Joshua Stancheva, Viktoriya G. Brown, Nick R. Cheung, Alan C. M. Miller, Elizabeth A. Zanetti, Giulia |
author_facet | Hutchings, Joshua Stancheva, Viktoriya G. Brown, Nick R. Cheung, Alan C. M. Miller, Elizabeth A. Zanetti, Giulia |
author_sort | Hutchings, Joshua |
collection | PubMed |
description | COPII mediates Endoplasmic Reticulum to Golgi trafficking of thousands of cargoes. Five essential proteins assemble into a two-layer architecture, with the inner layer thought to regulate coat assembly and cargo recruitment, and the outer coat forming cages assumed to scaffold membrane curvature. Here we visualise the complete, membrane-assembled COPII coat by cryo-electron tomography and subtomogram averaging, revealing the full network of interactions within and between coat layers. We demonstrate the physiological importance of these interactions using genetic and biochemical approaches. Mutagenesis reveals that the inner coat alone can provide membrane remodelling function, with organisational input from the outer coat. These functional roles for the inner and outer coats significantly move away from the current paradigm, which posits membrane curvature derives primarily from the outer coat. We suggest these interactions collectively contribute to coat organisation and membrane curvature, providing a structural framework to understand regulatory mechanisms of COPII trafficking and secretion. |
format | Online Article Text |
id | pubmed-8016994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80169942021-04-16 Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network Hutchings, Joshua Stancheva, Viktoriya G. Brown, Nick R. Cheung, Alan C. M. Miller, Elizabeth A. Zanetti, Giulia Nat Commun Article COPII mediates Endoplasmic Reticulum to Golgi trafficking of thousands of cargoes. Five essential proteins assemble into a two-layer architecture, with the inner layer thought to regulate coat assembly and cargo recruitment, and the outer coat forming cages assumed to scaffold membrane curvature. Here we visualise the complete, membrane-assembled COPII coat by cryo-electron tomography and subtomogram averaging, revealing the full network of interactions within and between coat layers. We demonstrate the physiological importance of these interactions using genetic and biochemical approaches. Mutagenesis reveals that the inner coat alone can provide membrane remodelling function, with organisational input from the outer coat. These functional roles for the inner and outer coats significantly move away from the current paradigm, which posits membrane curvature derives primarily from the outer coat. We suggest these interactions collectively contribute to coat organisation and membrane curvature, providing a structural framework to understand regulatory mechanisms of COPII trafficking and secretion. Nature Publishing Group UK 2021-04-01 /pmc/articles/PMC8016994/ /pubmed/33795673 http://dx.doi.org/10.1038/s41467-021-22110-6 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 Hutchings, Joshua Stancheva, Viktoriya G. Brown, Nick R. Cheung, Alan C. M. Miller, Elizabeth A. Zanetti, Giulia Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network |
title | Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network |
title_full | Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network |
title_fullStr | Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network |
title_full_unstemmed | Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network |
title_short | Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network |
title_sort | structure of the complete, membrane-assembled copii coat reveals a complex interaction network |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016994/ https://www.ncbi.nlm.nih.gov/pubmed/33795673 http://dx.doi.org/10.1038/s41467-021-22110-6 |
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