Chemical Probes of Escherichia coli Uncovered through Chemical-Chemical Interaction Profiling with Compounds of Known Biological Activity

被引:58
作者
Farha, Maya A. [1 ,2 ]
Brown, Eric D. [1 ,2 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Michael G DeGroote Inst Infect Dis Res, Hamilton, ON L8N 3Z5, Canada
来源
CHEMISTRY & BIOLOGY | 2010年 / 17卷 / 08期
基金
加拿大健康研究院;
关键词
STAPHYLOCOCCUS-AUREUS; INDUCED HAPLOINSUFFICIENCY; ANTIBACTERIAL COMPOUNDS; PROMISCUOUS INHIBITORS; BACTERICIDAL ACTIVITY; TOPOISOMERASE-IV; YEAST; IDENTIFICATION; TARGET; DAPTOMYCIN;
D O I
10.1016/j.chembiol.2010.06.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While cell-based screens have considerable power in identifying new chemical probes of biological systems and leads for new drugs, a major challenge to the utility of such compounds is in connecting phenotype with a cellular target. Here, we present a systematic study to elucidate the mechanism of action of uncharacterized inhibitors of the growth of Escherichia coli through careful analyses of interactions with compounds of known biological activity. We studied growth inhibition with a collection of 200 antibacterial compounds when systematically combined with a panel of 14 known antibiotics of diverse mechanism and chemical class. Our work revealed a high frequency of synergistic chemical-chemical interactions where the interaction profiles were unique to the various compound pairs. Thus, the work revealed that chemical-chemical interaction data provides a fingerprint of biological activity and testable hypotheses regarding the mechanism of action of the novel bioactive molecules. In the study reported here, we determined the mode of action of an inhibitor of folate biosynthesis and a DNA gyrase inhibitor. Moreover, we identified eight membrane-active compounds, found to be promiscuously synergistic with known bioactives.
引用
收藏
页码:852 / 862
页数:11
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