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Protected by Google reCAPTCHA v3.•Privacy•Terms Key Findings in This Report
• RACK1 is identified as a novel host interactor of CHIKV nsP4, regulating its stability via the ubiquitin-proteasome pathway.
• Harringtonolide disrupts RACK1-nsP4 interaction, promoting nsP4 degradation and reducing viral replication potential.
• Proteasome inhibitor MG132 reverses RACK1 inhibitor-induced nsP4 degradation, confirming proteasomal involvement.
• Targeting RACK1-nsP4 interaction offers a promising therapeutic strategy against chikungunya virus.