tetano
Editor, Senior Moderator
Virology
. 2025 Jan 17:604:110411.
doi: 10.1016/j.virol.2025.110411. Online ahead of print. Structural insights into nucleocapsid protein variability: Implications for PJ34 efficacy against SARS-CoV-2
Akima Yamamoto[SUP] 1 [/SUP], Haruki Ito[SUP] 2 [/SUP], Takemasa Sakaguchi[SUP] 3 [/SUP], Akifumi Higashiura[SUP] 4 [/SUP]
Affiliations
Human coronaviruses (HCoVs) include common cold viruses such as HCoV-229E, OC43, NL63 and HKU1 as well as MERS-CoV and SARS-CoV, which cause severe respiratory disease. Recently, SARS-CoV-2 caused a COVID-19 pandemic. The nucleocapsid (N) protein of coronaviruses, which is essential for RNA binding and homodimerization, has a highly conserved structure across viruses. Previous studies revealed that compound PJ34 is an inhibitor of nucleic acid binding to the N-terminal domain (NTD) of the HCoV-OC43 N protein, suggesting that it could block viral replication. However, testing with SARS-CoV-2 showed that PJ34 did not inhibit viral replication. Structural analysis suggests that the substitution of Tyr for Ala at position 50 (corresponding to Tyr63 in OC43), may affect the ability to interact with compounds such as PJ34, explaining its lack of efficacy. These findings underscore the importance of structure-based drug development targeting the N protein, which remains an important therapeutic target in all coronaviruses.
Keywords: COVID-19; N protein; PJ34; Protein structure; Structure–activity relationship; X-ray crystallography.
. 2025 Jan 17:604:110411.
doi: 10.1016/j.virol.2025.110411. Online ahead of print. Structural insights into nucleocapsid protein variability: Implications for PJ34 efficacy against SARS-CoV-2
Akima Yamamoto[SUP] 1 [/SUP], Haruki Ito[SUP] 2 [/SUP], Takemasa Sakaguchi[SUP] 3 [/SUP], Akifumi Higashiura[SUP] 4 [/SUP]
Affiliations
- PMID: 39848104
- DOI: 10.1016/j.virol.2025.110411
Human coronaviruses (HCoVs) include common cold viruses such as HCoV-229E, OC43, NL63 and HKU1 as well as MERS-CoV and SARS-CoV, which cause severe respiratory disease. Recently, SARS-CoV-2 caused a COVID-19 pandemic. The nucleocapsid (N) protein of coronaviruses, which is essential for RNA binding and homodimerization, has a highly conserved structure across viruses. Previous studies revealed that compound PJ34 is an inhibitor of nucleic acid binding to the N-terminal domain (NTD) of the HCoV-OC43 N protein, suggesting that it could block viral replication. However, testing with SARS-CoV-2 showed that PJ34 did not inhibit viral replication. Structural analysis suggests that the substitution of Tyr for Ala at position 50 (corresponding to Tyr63 in OC43), may affect the ability to interact with compounds such as PJ34, explaining its lack of efficacy. These findings underscore the importance of structure-based drug development targeting the N protein, which remains an important therapeutic target in all coronaviruses.
Keywords: COVID-19; N protein; PJ34; Protein structure; Structure–activity relationship; X-ray crystallography.