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Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus
SARS-CoV-2 infection has caused a global pandemic that has severely damaged both public health and the economy. The nucleocapsid protein of SARS-CoV-2 is multifunctional and plays an important role in ribonucleocapsid formation and viral genome replication. In order to elucidate its functions, inter...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465953/ https://www.ncbi.nlm.nih.gov/pubmed/34578187 http://dx.doi.org/10.3390/pathogens10091155 |
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author | Zheng, Xiaoqin Sun, Zeyu Yu, Liang Shi, Danrong Zhu, Miaojin Yao, Hangping Li, Lanjuan |
author_facet | Zheng, Xiaoqin Sun, Zeyu Yu, Liang Shi, Danrong Zhu, Miaojin Yao, Hangping Li, Lanjuan |
author_sort | Zheng, Xiaoqin |
collection | PubMed |
description | SARS-CoV-2 infection has caused a global pandemic that has severely damaged both public health and the economy. The nucleocapsid protein of SARS-CoV-2 is multifunctional and plays an important role in ribonucleocapsid formation and viral genome replication. In order to elucidate its functions, interaction partners of the SARS-CoV-2 N protein in human cells were identified via affinity purification and mass spectrometry. We identified 160 cellular proteins as interaction partners of the SARS-CoV-2 N protein in HEK293T and/or Calu-3 cells. Functional analysis revealed strong enrichment for ribosome biogenesis and RNA-associated processes, including ribonucleoprotein complex biogenesis, ribosomal large and small subunits biogenesis, RNA binding, catalysis, translation and transcription. Proteins related to virus defence responses, including MOV10, EIF2AK2, TRIM25, G3BP1, ZC3HAV1 and ZCCHC3 were also identified in the N protein interactome. This study comprehensively profiled the viral–host interactome of the SARS-CoV-2 N protein in human cells, and the findings provide the basis for further studies on the pathogenesis and antiviral strategies for this emerging infection. |
format | Online Article Text |
id | pubmed-8465953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84659532021-09-27 Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus Zheng, Xiaoqin Sun, Zeyu Yu, Liang Shi, Danrong Zhu, Miaojin Yao, Hangping Li, Lanjuan Pathogens Article SARS-CoV-2 infection has caused a global pandemic that has severely damaged both public health and the economy. The nucleocapsid protein of SARS-CoV-2 is multifunctional and plays an important role in ribonucleocapsid formation and viral genome replication. In order to elucidate its functions, interaction partners of the SARS-CoV-2 N protein in human cells were identified via affinity purification and mass spectrometry. We identified 160 cellular proteins as interaction partners of the SARS-CoV-2 N protein in HEK293T and/or Calu-3 cells. Functional analysis revealed strong enrichment for ribosome biogenesis and RNA-associated processes, including ribonucleoprotein complex biogenesis, ribosomal large and small subunits biogenesis, RNA binding, catalysis, translation and transcription. Proteins related to virus defence responses, including MOV10, EIF2AK2, TRIM25, G3BP1, ZC3HAV1 and ZCCHC3 were also identified in the N protein interactome. This study comprehensively profiled the viral–host interactome of the SARS-CoV-2 N protein in human cells, and the findings provide the basis for further studies on the pathogenesis and antiviral strategies for this emerging infection. MDPI 2021-09-08 /pmc/articles/PMC8465953/ /pubmed/34578187 http://dx.doi.org/10.3390/pathogens10091155 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zheng, Xiaoqin Sun, Zeyu Yu, Liang Shi, Danrong Zhu, Miaojin Yao, Hangping Li, Lanjuan Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus |
title | Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus |
title_full | Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus |
title_fullStr | Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus |
title_full_unstemmed | Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus |
title_short | Interactome Analysis of the Nucleocapsid Protein of SARS-CoV-2 Virus |
title_sort | interactome analysis of the nucleocapsid protein of sars-cov-2 virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465953/ https://www.ncbi.nlm.nih.gov/pubmed/34578187 http://dx.doi.org/10.3390/pathogens10091155 |
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