毒力
异源的
生物
基因
异源表达
调节器
化学
计算生物学
蜡螟
基因组
微生物学
体外
发光杆菌属
人类病原体
药物发现
肽
化学生物学
背景(考古学)
体外毒理学
细胞生物学
微生物毒素
体内
生物化学
作者
Yongchao Wang,Jinhuan Yin,Wei‐Ting Liao,Yanwei Gao,Yan Yao,Li Lü,Weixin Tao,Fan Zhang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-04
卷期号:64 (49): e202514683-e202514683
被引量:1
标识
DOI:10.1002/anie.202514683
摘要
The global threat of MRSA demands innovative anti-virulence strategies. Caseinolytic peptidase P (ClpP), a central virulence regulator in MRSA, represents an attractive yet underexploited target. Here, we developed a discovery platform integrating self-resistance gene-guided genome mining with dual functional screening, combining fluorometric-based assay and counter-screening against ADEP-induced ClpP activation. This led to the discovery of streptoclipamides A-G, novel hybrid polyketide-nonribosomal peptide ClpP inhibitors from str BGC, validated via heterologous expression and gene knockout. Structure-activity relationship studies enabled by engineered analogues identified key pharmacophores. Streptoclipamide A potently inhibits ClpP (IC50 = 480 nM) by engaging Thr72 via its C-21 hydroxyl group, confirmed by biophysics and self-resistance-conferring T72P mutation. Streptoclipamide A suppressed MRSA virulence in vitro by reducing critical toxin production, including α-hemolysin, and demonstrated protection in Galleria mellonella and murine pneumonia models. This work expands chemical diversity of ClpP-targeting agents, and establishes a genome mining-driven platform for discovering new therapeutics against antibiotic-resistant pathogens.
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