Chemokines simultaneously bind SARS-CoV-2 nucleocapsid protein RNA-binding and dimerization domains

Viruses express chemokine (CHK)-binding proteins to interfere with the host CHK network and thereby modulate leukocyte migration. SARS-CoV-2 Nucleocapsid (N) protein binds a subset of human CHKs with high affinity, inhibiting their chemoattractant properties. Here, we report that both N's RNA-binding and dimerization domains participate individually in CHK binding. CHKs typically possess independent sites for binding glycosaminoglycans (GAG) and their receptor proteins. We show that the interaction with the N protein occurs through the CHK GAG-binding site, pointing the way to developing compounds that block this interaction for potential anti-coronavirus therapeutics.

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Publication Details

Journal
Virology Journal
Published
2025-03-17
DOI
https://doi.org/10.1186/s12985-025-02658-1
Citations
1
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
1.40

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article

Chemokines simultaneously bind SARS-CoV-2 nucleocapsid protein RNA-binding and dimerization domains

Jonathan Wilson Yewdell, Alberto Domingo López-Muñoz
1 citations
Virology Journal
SARS-CoV-2 and COVID-19 Research
1.40
article

Chemokines simultaneously bind SARS-CoV-2 nucleocapsid protein RNA-binding and dimerization domains

Jonathan Wilson Yewdell, Alberto Domingo López-Muñoz
article en
1 citations

Abstract

Viruses express chemokine (CHK)-binding proteins to interfere with the host CHK network and thereby modulate leukocyte migration. SARS-CoV-2 Nucleocapsid (N) protein binds a subset of human CHKs with high affinity, inhibiting their chemoattractant properties. Here, we report that both N's RNA-binding and dimerization domains participate individually in CHK binding. CHKs typically possess independent sites for binding glycosaminoglycans (GAG) and their receptor proteins. We show that the interaction with the N protein occurs through the CHK GAG-binding site, pointing the way to developing compounds that block this interaction for potential anti-coronavirus therapeutics.

Virology JournalVol. 22(1)
National Institutes of Health (US), National Institute of Allergy and Infectious Diseases (US)
National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 23%
SARS-CoV-2 and COVID-19 Research
1.40
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Chemokines simultaneously bind SARS-CoV-2 nucleocapsid protein RNA-binding and dimerization domains — Jonathan Wilson Yewdell, Alberto Domingo López-Muñoz · Virology Journal (2025) | TGRS Research Map | TGRS