Target-Based Whole-Cell Screening by 1H NMR Spectroscopy

被引:16
|
作者
Ma, Junhe [1 ]
Cao, Qing [1 ]
McLeod, Sarah M. [2 ]
Ferguson, Keith [2 ]
Gao, Ning [1 ]
Breeze, Alexander L. [3 ]
Hu, Jun [1 ]
机构
[1] AstraZeneca R&D Boston, Discovery Sci, Waltham, MA 02451 USA
[2] AstraZeneca R&D Boston, Infect Innovat Med, Waltham, MA 02451 USA
[3] AstraZeneca R&D, Discovery Sci, Macclesfield SK10 4TG, Cheshire, England
关键词
drug discovery; invivo methods; New Delhi metallo--lactamase; NMR spectroscopy; whole-cell screening; BETA-LACTAMASE INHIBITORS; DRUG DISCOVERY;
D O I
10.1002/anie.201410701
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An NMR-based approach marries the two traditional screening technologies (phenotypic and target-based screening) to find compounds inhibiting a specific enzymatic reaction in bacterial cells. Building on a previous study in which it was demonstrated that hydrolytic decomposition of meropenem in living Escherichia coli cells carrying New Delhi metallo--lactamase subclass 1 (NDM-1) can be monitored in real time by NMR spectroscopy, we designed a cell-based NMR screening platform. A strong NDM-1 inhibitor was identified with cellular IC50 of 0.51M, which is over 300-fold more potent than captopril, a known NDM-1 inhibitor. This new screening approach has great potential to be applied to targets in other cell types, such as mammalian cells, and to targets that are only stable or functionally competent in the cellular environment.
引用
收藏
页码:4764 / 4767
页数:4
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