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模拟抗生素和细胞毒性异喹啉对金黄色葡萄球菌、表皮葡萄球菌及哺乳动物细胞的作用。

Modelling antibiotic and cytotoxic isoquinoline effects in Staphylococcus aureus, Staphylococcus epidermidis and mammalian cells.

作者信息

Cecil Alexander, Ohlsen Knut, Menzel Thomas, François Patrice, Schrenzel Jacques, Fischer Adrien, Dörries Kirsten, Selle Martina, Lalk Michael, Hantzschmann Julia, Dittrich Marcus, Liang Chunguang, Bernhardt Jörg, Ölschläger Tobias A, Bringmann Gerhard, Bruhn Heike, Unger Matthias, Ponte-Sucre Alicia, Lehmann Leane, Dandekar Thomas

机构信息

Department of Bioinformatics, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.

University of Würzburg, Institute for Molecular-Infection Biology, 97070 Würzburg, Germany.

出版信息

Int J Med Microbiol. 2015 Jan;305(1):96-109. doi: 10.1016/j.ijmm.2014.11.006. Epub 2014 Nov 27.

Abstract

Isoquinolines (IQs) are natural substances with an antibiotic potential we aim to optimize. Specifically, IQ-238 is a synthetic analog of the novel-type N,C-coupled naphthylisoquinoline (NIQ) alkaloid ancisheynine. Recently, we developed and tested other IQs such as IQ-143. By utilizing genome-wide gene expression data, metabolic network modelling and Voronoi tessalation based data analysis - as well as cytotoxicity measurements, chemical properties calculations and principal component analysis of the NIQs - we show that IQ-238 has strong antibiotic potential for staphylococci and low cytotoxicity against murine or human cells. Compared to IQ-143, systemic effects are less pronounced. Most enzyme activity changes due to IQ-238 are located in the carbohydrate metabolism. Validation includes metabolite measurements on biological replicates. IQ-238 delineates key properties and a chemical space for a good therapeutic window. The combination of analysis methods allows suggestions for further lead development and yields an in-depth look at staphylococcal adaptation and network changes after antibiosis. Results are compared to eukaryotic host cells.

摘要

异喹啉(IQs)是具有抗生素潜力的天然物质,我们旨在对其进行优化。具体而言,IQ - 238是新型N,C - 偶联萘基异喹啉(NIQ)生物碱安西辛宁的合成类似物。最近,我们开发并测试了其他IQs,如IQ - 143。通过利用全基因组基因表达数据、代谢网络建模以及基于Voronoi镶嵌的数据分析,以及细胞毒性测量、化学性质计算和NIQs的主成分分析,我们表明IQ - 238对葡萄球菌具有强大的抗生素潜力,对鼠类或人类细胞的细胞毒性较低。与IQ - 143相比,全身效应不太明显。由于IQ - 238导致的大多数酶活性变化位于碳水化合物代谢中。验证包括对生物重复样本的代谢物测量。IQ - 238描绘了良好治疗窗口的关键特性和化学空间。分析方法的组合为进一步的先导物开发提供了建议,并深入了解了葡萄球菌在抗菌后的适应性和网络变化。将结果与真核宿主细胞进行了比较。

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