部分
化学
生物化学
合理设计
真核生物
结构-活动关系
共价键
原核生物
酶
抗生素
立体化学
组合化学
活动站点
结合位点
药品
血浆蛋白结合
效力
生物物理学
细菌
药物开发
重组DNA
生物
计算生物学
超家族
选择性
抗生素耐药性
药物发现
蛋白质结构
作者
Zilu Wang,Zhengxuan Zhang,Mingyu Xia,Min Fang,Haoran Xu,Hang Qiao,Wenping Ding,Jiancheng Huang,Guozheng Li,Ke Luo,Wen Liu,Jing Wang,Biao Yu,Pengfei Fang
摘要
The widespread emergence of antibiotic resistance necessitates the development of novel agents with unique mechanisms of action. Obafluorin (OB), a natural β-lactone antibiotic, is a covalent inhibitor of threonyl-tRNA synthetase (ThrRS), but the high conservation of the active site between prokaryote and eukaryote ThrRSs results in minimal selectivity, hindering the therapeutic potential of OB. Here, we report a structure dynamics-based design strategy that transforms OB into a selective antibacterial agent. OB inhibits human and bacterial ThrRSs with nearly equal potency due to identical binding modes. The nitrophenyl moiety of OB is proposed as a 'kinetic sensor' that discriminates between sensitive and resistant ThrRS paralogs. Guided by this insight, we designed a series of OB analogs through rational modification of this moiety. Among them, OB-D4 bearing a para-methoxyphenyl group in place of the nitrophenyl group, exhibited a 241-fold selectivity for bacterial over human ThrRS, along with a markedly improved safety profile with minimal cytotoxicity. In a murine skin infection model, OB-D4 effectively eradicated pathogens, resolving inflammation, and promoting wound healing. Together, this work establishes a 'kinetic sensor' strategy for achieving species selectivity, turning a fundamental challenge in drug discovery-high active-site conservation-into an exploitable opportunity based on dynamic differences.
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