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An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking
β-Coronaviruses such as SARS-CoV-2 hijack coatomer protein-I (COPI) for spike protein retrograde trafficking to the progeny assembly site in endoplasmic reticulum-Golgi intermediate compartment (ERGIC). However, limited residue-level details are available into how the spike interacts with COPI. Here...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825798/ https://www.ncbi.nlm.nih.gov/pubmed/35136165 http://dx.doi.org/10.1038/s42003-022-03063-y |
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author | Dey, Debajit Singh, Suruchi Khan, Saif Martin, Matthew Schnicker, Nicholas J. Gakhar, Lokesh Pierce, Brian G. Hasan, S. Saif |
author_facet | Dey, Debajit Singh, Suruchi Khan, Saif Martin, Matthew Schnicker, Nicholas J. Gakhar, Lokesh Pierce, Brian G. Hasan, S. Saif |
author_sort | Dey, Debajit |
collection | PubMed |
description | β-Coronaviruses such as SARS-CoV-2 hijack coatomer protein-I (COPI) for spike protein retrograde trafficking to the progeny assembly site in endoplasmic reticulum-Golgi intermediate compartment (ERGIC). However, limited residue-level details are available into how the spike interacts with COPI. Here we identify an extended COPI binding motif in the spike that encompasses the canonical K-x-H dibasic sequence. This motif demonstrates selectivity for αCOPI subunit. Guided by an in silico analysis of dibasic motifs in the human proteome, we employ mutagenesis and binding assays to show that the spike motif terminal residues are critical modulators of complex dissociation, which is essential for spike release in ERGIC. αCOPI residues critical for spike motif binding are elucidated by mutagenesis and crystallography and found to be conserved in the zoonotic reservoirs, bats, pangolins, camels, and in humans. Collectively, our investigation on the spike motif identifies key COPI binding determinants with implications for retrograde trafficking. |
format | Online Article Text |
id | pubmed-8825798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88257982022-02-17 An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking Dey, Debajit Singh, Suruchi Khan, Saif Martin, Matthew Schnicker, Nicholas J. Gakhar, Lokesh Pierce, Brian G. Hasan, S. Saif Commun Biol Article β-Coronaviruses such as SARS-CoV-2 hijack coatomer protein-I (COPI) for spike protein retrograde trafficking to the progeny assembly site in endoplasmic reticulum-Golgi intermediate compartment (ERGIC). However, limited residue-level details are available into how the spike interacts with COPI. Here we identify an extended COPI binding motif in the spike that encompasses the canonical K-x-H dibasic sequence. This motif demonstrates selectivity for αCOPI subunit. Guided by an in silico analysis of dibasic motifs in the human proteome, we employ mutagenesis and binding assays to show that the spike motif terminal residues are critical modulators of complex dissociation, which is essential for spike release in ERGIC. αCOPI residues critical for spike motif binding are elucidated by mutagenesis and crystallography and found to be conserved in the zoonotic reservoirs, bats, pangolins, camels, and in humans. Collectively, our investigation on the spike motif identifies key COPI binding determinants with implications for retrograde trafficking. Nature Publishing Group UK 2022-02-08 /pmc/articles/PMC8825798/ /pubmed/35136165 http://dx.doi.org/10.1038/s42003-022-03063-y 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 Dey, Debajit Singh, Suruchi Khan, Saif Martin, Matthew Schnicker, Nicholas J. Gakhar, Lokesh Pierce, Brian G. Hasan, S. Saif An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking |
title | An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking |
title_full | An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking |
title_fullStr | An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking |
title_full_unstemmed | An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking |
title_short | An extended motif in the SARS-CoV-2 spike modulates binding and release of host coatomer in retrograde trafficking |
title_sort | extended motif in the sars-cov-2 spike modulates binding and release of host coatomer in retrograde trafficking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825798/ https://www.ncbi.nlm.nih.gov/pubmed/35136165 http://dx.doi.org/10.1038/s42003-022-03063-y |
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