抗生素
化学
抗生素耐药性
细菌
孔蛋白
共价键
细菌外膜
细胞内
生物物理学
纳米技术
微生物学
生物化学
基因
大肠杆菌
遗传学
生物
材料科学
有机化学
作者
Jinming Chang,Yi Chen,Zhou Xu,Zhonghui Wang,Qi Zeng,Haojun Fan
标识
DOI:10.1021/acs.bioconjchem.7b00599
摘要
Bacterial resistance is emerging as a global threat, stemming partially from continuous exposure of pathogens to antibiotics of sublethal concentrations. Thus, novel molecular approaches capable of inactivating antibiotics, which prevent their final build-up in the environment, are highly desirable. Here, we report a proof-of-principle demonstration of a mechanically new strategy for switchable control of antibiotic activity, which regulates drug uptake across the outer membrane of Gram-negative bacteria by externally triggered shape shifting of a short, covalently attached "tail". The rationale behind this strategy is grounded in the size-selectivity of porin channels exploited by a large proportion of antibiotics for accessing intracellular targets, thus representing a general approach to control antibiotic availability in the environment which alleviates undue selection pressure for resistance.
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