细菌
抗菌剂
生物
噬菌体展示
计算生物学
噬菌体疗法
小分子
细菌细胞结构
药物发现
合成生物学
噬菌体
微生物学
大肠杆菌
遗传学
生物化学
基因
抗体
作者
Xing Wan,Hanne Hendrix,Mikael Skurnik,Rob Lavigne
标识
DOI:10.1016/j.copbio.2020.08.015
摘要
The deeply intertwined evolutionary history between bacteriophages and bacteria has endowed phages with highly specific mechanisms to hijack bacterial cell metabolism for their propagation. Here, we present a comprehensive, phage-driven strategy to reveal novel antibacterial targets by the exploitation of phage-bacteria interactions. This strategy will enable the design of small molecules, which mimic the inhibitory phage proteins, and allow the subsequent hit-to-lead development of these antimicrobial compounds. This proposed small molecule approach is distinct from phage therapy and phage enzyme-based antimicrobials and may produce a more sustainable generation of new antibiotics that exploit novel bacterial targets and act in a pathogen-specific manner.
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