SARS-CoV-2 Nonstructural Protein 3 Remodels the Phosphorylation of Target Proteins via Protein-Protein Interactions
Yang, H.; Peng, D.; Martinez-Sobrido, L.; Ye, C.
Show abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19), triggered a global pandemic with a significant impact on human health. The molecular basis of its pathogenicity remains incompletely understood. The viral nucleocapsid (N) protein, the most abundant protein expressed during SARS-CoV-2 infection, is thought to contribute to disease progression. Yet, its interaction network in the context of viral infection remains largely unexplored. Here, we generated a recombinant (r)SARS-CoV-2 expressing a Strep-tagged N protein by using a reverse genetics system. Affinity purification and mass spectrometry identified an interaction between SARS-CoV-2 N protein and the nonstructural protein 3 (NSP3). Domain mapping revealed that the N dimerization domain and the N-terminal region of NSP3 mediate this interaction. Notably, an N protein mutant lacking its N-terminal domain exhibited enhanced binding to NSP3 and underwent dephosphorylation, implicating NSP3 as a potential viral phosphatase. We further found that NSP3 interacts with Interferon Regulatory Factor 3 (IRF3), a key transcription factor involved in host type I interferon (IFN-/{beta}) antiviral response. SARS-CoV-2 NSP3 expression suppressed poly(I:C)-induced IRF3 phosphorylation and broadly reduced cellular phosphorylation levels in a dose-dependent manner. These findings suggest that SARS-CoV-2 NSP3 modulates host phosphorylation dynamics to subvert antiviral signaling and facilitate viral replication. SIGNIFICANCEUnderstanding virus-host and virus-virus interactions is essential for elucidating the mechanisms of viral replication and immune evasion. Previous studies using individually expressed SARS-CoV-2 proteins have identified host interacting factors but have largely overlooked interactions between viral proteins. Here, we engineered a recombinant SARS-CoV-2 virus expressing Strep-tagged nucleocapsid (N) protein, allowing the identification of both viral and host proteins interacting with N during live infection. We discovered an interaction between N and nonstructural protein 3 (NSP3), revealing a previously unrecognized role for NSP3 in modulating protein phosphorylation, interacting with Interferon Regulatory Factor 3 (IRF3), and regulating the innate immune response. This work demonstrates a powerful strategy for dissecting protein interaction networks during SARS-CoV-2 infection and identifies potential targets for therapeutic intervention.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Thiopurines activate an antiviral unfolded protein response that blocks viral glycoprotein accumulation in cell culture infection model 97%
- Mutations differentially affecting the coronavirus Mac1 ADP-ribose binding and hydrolysis activities indicate that it promotes multiple stages of the viral replication cycle 97%
- The leader proteins of Theiler's virus and Boone cardiovirus use a combination of Short Linear Motifs (SLiMs) to target RSK kinases to the nuclear pore complex. 97%
Similar papers in this journal
- Cardiovirus-Mediated PKR Inhibition Results from Nucleocytoplasmic Trafficking Disruption 97%
- SARS-CoV-2 nucleocapsid protein inhibits the PKR-mediated integrated stress response through RNA-binding domain N2b 97%
- Nuclear dengue virus NS5 antagonizes expression of PAF1-dependent immune response genes 97%
Similar papers in this journal
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.