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A BioID-derived proximity interactome for SARS-CoV-2 proteins

The novel coronavirus SARS-CoV-2 is responsible for the ongoing COVID-19 pandemic and has caused a major health and economic burden worldwide. Understanding how SARS-CoV-2 viral proteins behave in host cells can reveal underlying mechanisms of pathogenesis and assist in development of antiviral ther...

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Autores principales: May, Danielle G., Martin-Sancho, Laura, Anschau, Valesca, Liu, Sophie, Chrisopulos, Rachel J., Scott, Kelsey L., Halfmann, Charles T., Peña, Ramon Díaz, Pratt, Dexter, Campos, Alexandre R., Roux, Kyle J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8475972/
https://www.ncbi.nlm.nih.gov/pubmed/34580671
http://dx.doi.org/10.1101/2021.09.17.460814
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author May, Danielle G.
Martin-Sancho, Laura
Anschau, Valesca
Liu, Sophie
Chrisopulos, Rachel J.
Scott, Kelsey L.
Halfmann, Charles T.
Peña, Ramon Díaz
Pratt, Dexter
Campos, Alexandre R.
Roux, Kyle J.
author_facet May, Danielle G.
Martin-Sancho, Laura
Anschau, Valesca
Liu, Sophie
Chrisopulos, Rachel J.
Scott, Kelsey L.
Halfmann, Charles T.
Peña, Ramon Díaz
Pratt, Dexter
Campos, Alexandre R.
Roux, Kyle J.
author_sort May, Danielle G.
collection PubMed
description The novel coronavirus SARS-CoV-2 is responsible for the ongoing COVID-19 pandemic and has caused a major health and economic burden worldwide. Understanding how SARS-CoV-2 viral proteins behave in host cells can reveal underlying mechanisms of pathogenesis and assist in development of antiviral therapies. Here we use BioID to map the SARS-CoV-2 virus-host interactome using human lung cancer derived A549 cells expressing individual SARS-CoV-2 viral proteins. Functional enrichment analyses revealed previously reported and unreported cellular pathways that are in association with SARS-CoV-2 proteins. We have also established a website to host the proteomic data to allow for public access and continued analysis of host-viral protein associations and whole-cell proteomes of cells expressing the viral-BioID fusion proteins. Collectively, these studies provide a valuable resource to potentially uncover novel SARS-CoV-2 biology and inform development of antivirals.
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spelling pubmed-84759722021-09-28 A BioID-derived proximity interactome for SARS-CoV-2 proteins May, Danielle G. Martin-Sancho, Laura Anschau, Valesca Liu, Sophie Chrisopulos, Rachel J. Scott, Kelsey L. Halfmann, Charles T. Peña, Ramon Díaz Pratt, Dexter Campos, Alexandre R. Roux, Kyle J. bioRxiv Article The novel coronavirus SARS-CoV-2 is responsible for the ongoing COVID-19 pandemic and has caused a major health and economic burden worldwide. Understanding how SARS-CoV-2 viral proteins behave in host cells can reveal underlying mechanisms of pathogenesis and assist in development of antiviral therapies. Here we use BioID to map the SARS-CoV-2 virus-host interactome using human lung cancer derived A549 cells expressing individual SARS-CoV-2 viral proteins. Functional enrichment analyses revealed previously reported and unreported cellular pathways that are in association with SARS-CoV-2 proteins. We have also established a website to host the proteomic data to allow for public access and continued analysis of host-viral protein associations and whole-cell proteomes of cells expressing the viral-BioID fusion proteins. Collectively, these studies provide a valuable resource to potentially uncover novel SARS-CoV-2 biology and inform development of antivirals. Cold Spring Harbor Laboratory 2021-09-21 /pmc/articles/PMC8475972/ /pubmed/34580671 http://dx.doi.org/10.1101/2021.09.17.460814 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
May, Danielle G.
Martin-Sancho, Laura
Anschau, Valesca
Liu, Sophie
Chrisopulos, Rachel J.
Scott, Kelsey L.
Halfmann, Charles T.
Peña, Ramon Díaz
Pratt, Dexter
Campos, Alexandre R.
Roux, Kyle J.
A BioID-derived proximity interactome for SARS-CoV-2 proteins
title A BioID-derived proximity interactome for SARS-CoV-2 proteins
title_full A BioID-derived proximity interactome for SARS-CoV-2 proteins
title_fullStr A BioID-derived proximity interactome for SARS-CoV-2 proteins
title_full_unstemmed A BioID-derived proximity interactome for SARS-CoV-2 proteins
title_short A BioID-derived proximity interactome for SARS-CoV-2 proteins
title_sort bioid-derived proximity interactome for sars-cov-2 proteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8475972/
https://www.ncbi.nlm.nih.gov/pubmed/34580671
http://dx.doi.org/10.1101/2021.09.17.460814
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