Systematic Studies on the Anti-SARS-CoV-2 Mechanisms of Tea Polyphenol-Related Natural Products.
Chen-Wei LiTai-Ling ChaoChin-Lan LaiCheng-Chin LinMax Yu-Chen PanChieh-Ling ChengChih-Jung KuoLily Hui-Ching WangSui-Yuan ChangPo-Huang LiangPublished in: ACS omega (2024)
The causative pathogen of COVID-19, severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), utilizes the receptor-binding domain (RBD) of the spike protein to bind to human receptor angiotensin-converting enzyme 2 (ACE2). Further cleavage of spike by human proteases furin, TMPRSS2, and/or cathepsin L facilitates viral entry into the host cells for replication, where the maturation of polyproteins by 3C-like protease (3CL pro ) and papain-like protease (PL pro ) yields functional nonstructural proteins (NSPs) such as RNA-dependent RNA polymerase (RdRp) to synthesize mRNA of structural proteins. By testing the tea polyphenol-related natural products through various assays, we found that the active antivirals prevented SARS-CoV-2 entry by blocking the RBD/ACE2 interaction and inhibiting the relevant human proteases, although some also inhibited the viral enzymes essential for replication. Due to their multitargeting properties, these compounds were often misinterpreted for their antiviral mechanisms. In this study, we provide a systematic protocol to check and clarify their anti-SARS-CoV-2 mechanisms, which should be applicable for all of the antivirals.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- angiotensin converting enzyme
- endothelial cells
- angiotensin ii
- binding protein
- randomized controlled trial
- coronavirus disease
- pluripotent stem cells
- signaling pathway
- anti inflammatory
- high throughput
- protein protein
- single cell
- dna binding
- candida albicans
- case control
- nucleic acid