抗菌剂
细菌
抗生素
金黄色葡萄球菌
微生物学
抗生素耐药性
生物
革兰氏阴性菌
作用机理
体内
大肠杆菌
体外
生物化学
生物技术
基因
遗传学
作者
G.-M. Qi,X.L. Liu,Hao Li,Yunyun Qian,Can Liu,Jiahao Zhuang,Leilei Shi,Bin Liu
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-04-11
卷期号:11 (15)
标识
DOI:10.1126/sciadv.adp9448
摘要
Because of the rapid emergence of antibiotic-resistant bacteria, there is a growing need to discover antibacterial agents. Here, we design and synthesize a compound of TPA2PyBu that kills both Gram-negative and Gram-positive bacteria with an undetectably low drug resistance. Comprehensive analyses reveal that the antimicrobial activity of TPA2PyBu proceeds via a unique dual mechanism by damaging bacterial membrane integrity and inducing DNA aggregation. TPA2PyBu could provide imaging specificity that differentiates bacterial infection from inflammation and cancer. High in vivo treatment efficacy of TPA2PyBu was achieved in methicillin-resistant Staphylococcus aureus infection mouse models. This promising antimicrobial agent suggests that combining multiple mechanisms of action into a single molecule can be an effective approach to address challenging bacterial infections.
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