Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Dey, Debajit, Singh, Suruchi, Khan, Saif, Martin, Matthew, Schnicker, Nicholas J., Gakhar, Lokesh, Pierce, Brian G., Hasan, S. Saif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
_version_ 1784647309152223232
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
work_keys_str_mv AT deydebajit anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT singhsuruchi anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT khansaif anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT martinmatthew anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT schnickernicholasj anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT gakharlokesh anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT piercebriang anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT hasanssaif anextendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT deydebajit extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT singhsuruchi extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT khansaif extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT martinmatthew extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT schnickernicholasj extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT gakharlokesh extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT piercebriang extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking
AT hasanssaif extendedmotifinthesarscov2spikemodulatesbindingandreleaseofhostcoatomerinretrogradetrafficking