{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,31]],"date-time":"2026-08-31T09:27:49Z","timestamp":1788168469760,"version":"build-2803163510"},"reference-count":47,"publisher":"MDPI AG","issue":"2","license":[{"start":{"date-parts":[[2026,1,9]],"date-time":"2026-01-09T00:00:00Z","timestamp":1767916800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["IJMS"],"abstract":"<jats:p>The SARS-CoV-2 nucleocapsid protein (Np) plays multifunctional roles in the viral life cycle. By interacting with host cellular proteins, Np regulates viral RNA transcription, replication, and immune evasion. It controls genome packaging and counteracts host RNA interference mediated antiviral responses through its RNA binding activity. Previous studies revealed a physical interaction between Np and DDX3X, a human DEAD-box RNA helicase that facilitates the replication of several viruses. This interaction enhances Np affinity for double-stranded RNA and inhibits DDX3X helicase activity. Since Np-RNA binding activity promotes ribonucleoprotein complex formation, targeting this interaction is a promising antiviral strategy. We generated truncated protein variants to define interaction regions between Np and DDX3X. Using AlphaFold modelling, we identified RecA2 as the key DDX3X domain involved in Np binding. Finally, to disrupt Np-RNA complex formation, we screened a small molecule library of putative binders of Np N-terminal region and identified two candidate inhibitors for further development.<\/jats:p>","DOI":"10.3390\/ijms27020672","type":"journal-article","created":{"date-parts":[[2026,1,9]],"date-time":"2026-01-09T10:35:52Z","timestamp":1767954952000},"page":"672","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Dissecting the Interaction Domains of SARS-CoV-2 Nucleocapsid Protein and Human RNA Helicase DDX3X and Search for Potential Inhibitors"],"prefix":"10.3390","volume":"27","author":[{"ORCID":"https:\/\/orcid.org\/0009-0000-2233-0762","authenticated-orcid":false,"given":"Camilla","family":"Lodola","sequence":"first","affiliation":[{"name":"Institute of Molecular Genetics IGM-CNR \u2018Luigi Luca Cavalli-Sforza\u2019, Via Abbiategrasso 207, I-27100 Pavia, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7731-8621","authenticated-orcid":false,"given":"Maria Michela","family":"Pallotta","sequence":"additional","affiliation":[{"name":"Institute of Molecular Genetics IGM-CNR \u2018Luigi Luca Cavalli-Sforza\u2019, Via Abbiategrasso 207, I-27100 Pavia, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9598-2339","authenticated-orcid":false,"given":"Fabrizio","family":"Manetti","sequence":"additional","affiliation":[{"name":"Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, I-53100 Siena, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5976-780X","authenticated-orcid":false,"given":"Paolo","family":"Governa","sequence":"additional","affiliation":[{"name":"Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, I-53100 Siena, Italy"},{"name":"Department of Food and Drug, University of Parma, Parco Area delle Scienze 27\/A, I-43124 Parma, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emmanuele","family":"Crespan","sequence":"additional","affiliation":[{"name":"Institute of Molecular Genetics IGM-CNR \u2018Luigi Luca Cavalli-Sforza\u2019, Via Abbiategrasso 207, I-27100 Pavia, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Giovanni","family":"Maga","sequence":"additional","affiliation":[{"name":"Institute of Molecular Genetics IGM-CNR \u2018Luigi Luca Cavalli-Sforza\u2019, Via Abbiategrasso 207, I-27100 Pavia, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4570-1885","authenticated-orcid":false,"given":"Massimiliano","family":"Secchi","sequence":"additional","affiliation":[{"name":"Institute of Molecular Genetics IGM-CNR \u2018Luigi Luca Cavalli-Sforza\u2019, Via Abbiategrasso 207, I-27100 Pavia, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2026,1,9]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"110607","DOI":"10.1016\/j.virol.2025.110607","article-title":"SARS-CoV-2 host-pathogen interactome: Insights into more players during pathogenesis","volume":"610","author":"Mothae","year":"2025","journal-title":"Virology"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"290","DOI":"10.1093\/nar\/gkac1179","article-title":"Structural domains of SARS-CoV-2 nucleocapsid protein coordinate to compact long nucleic acid substrates","volume":"51","author":"Morse","year":"2023","journal-title":"Nucleic Acids Res."},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"6647","DOI":"10.1093\/nar\/gkae256","article-title":"Assembly of SARS-CoV-2 nucleocapsid protein with nucleic acid","volume":"52","author":"Zhao","year":"2024","journal-title":"Nucleic Acids Res."},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"107834","DOI":"10.1016\/j.jbc.2024.107834","article-title":"Structural basis for the participation of the SARS-CoV-2 nucleocapsid protein in the template switch mechanism and genomic RNA reorganization","volume":"300","author":"Bezerra","year":"2024","journal-title":"J. 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