Rational design of small molecules that modulate the transcriptional function of the response regulator PhoP

被引:7
|
作者
Qing, Xiaoyu [1 ]
De Weerdt, Ami [2 ]
De Maeyer, Marc [1 ]
Steenackers, Hans [2 ]
Voet, Arnout [1 ]
机构
[1] Univ Leuven, Dept Chem, Lab Biomol Modelling & Design, Celestijnenlaan 200G,Bus2403, Heverlee, Belgium
[2] Univ Leuven, Ctr Microbial & Plant Genet, Kasteelpk Arenberg 20,Bus2406, Leuven, Belgium
关键词
Computational drug design; Pharmacophore modelling; PPI modulators; PhoP; ENTERICA SEROVAR TYPHIMURIUM; SALMONELLA-ENTERICA; HOT-SPOTS; DRUG DISCOVERY; VIRULENCE; INTERFACES; EVOLUTION; PROTEINS; DOCKING; SYSTEM;
D O I
10.1016/j.bbrc.2017.11.037
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
The response regulator PhoP, which is part of the PhoP/PhoQ two-component system, regulates the expression of multiple genes involved in controlling virulence in Salmonella enterica serovar Typhimurium and other species of Gram-negative bacteria. Modulating the phosphorylation-mediated dimerization in the receiver domain may interfere with the transcriptional function of PhoP. In this study, we analyzed the therapeutic potential of the PhoP receiver domain by exploring it as a potential target for drug design. The structural information was then applied to identify the first hit compounds from commercial chemical libraries by combining pharmacophore modelling and docking methods with a GFP (Green Fluorescent Protein)-based promoter-fusion bioassay. In total, one hundred and forty compounds were selected, purchased, and tested for biological activity. Several novel scaffolds showed acceptable potency to modulate the transcriptional function of PhoP, either by enhancing or inhibiting the expression of PhoP-dependent genes. These compounds may be used as the starting point for developing modulators that target the protein-protein interface of the PhoP protein as an alternative strategy against antibiotic resistance. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:375 / 381
页数:7
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