Suppr超能文献

利用液相色谱-质谱联用技术开发一种检测恶性疟原虫谷胱甘肽还原酶抑制剂的功能测定方法。

Development of a functional assay to detect inhibitors of Plasmodium falciparum glutathione reductase utilizing liquid chromatography-mass spectrometry.

作者信息

Burkard Lexi, Scheuermann Alexis, Simithy Johayra, Calderón Angela I

机构信息

Department of Drug Discovery and Development, Harrison School of Pharmacy, 4306 Walker Building, Auburn University, Auburn, AL, 36849, USA.

出版信息

Biomed Chromatogr. 2016 Apr;30(4):543-7. doi: 10.1002/bmc.3580. Epub 2015 Sep 18.

Abstract

Plasmodium falciparum (Pf) like most other organisms, has a sophisticated antioxidant system, part of which includes glutathione reductase (GR). GR works by recycling toxic glutathione disulfide to glutathione, thereby reducing reactive oxygen species and making a form of glutathione (GSH) the parasite can use. Inhibition of this enzyme in Pf impedes parasite growth. In addition, it has been confirmed that PfGR is not identical to human GR. Thus, PfGR is an excellent target for antimalarial drug development. A functional assay utilizing liquid chromatography-mass spectrometry was developed to specifically identify and evaluate inhibitors of PfGR. Using recombinant PfGR enzyme and 1,4-naphthoquinone (1) as a reference compound and 4-nitrobenzothiadiazole (2) and methylene blue (3) as additional compounds, we quantified the concentration of GSH produced compared with a control to determine the inhibitory effect of these compounds. Our results coincide with that presented in literature: compounds 1-3 inhibit PfGR with IC50 values of 2.71, 8.38, and 19.23 µm, respectively. Good precision for this assay was exhibited by low values of intraday and interday coefficient of variation (3.1 and 2.4%, respectively). Thus, this assay can be used to screen for other potential inhibitors of PfGR quickly and accurately.

摘要

恶性疟原虫(Pf)与大多数其他生物体一样,拥有一套复杂的抗氧化系统,其中一部分包括谷胱甘肽还原酶(GR)。GR通过将有毒的谷胱甘肽二硫化物循环转化为谷胱甘肽来发挥作用,从而减少活性氧物种,并生成寄生虫能够利用的一种谷胱甘肽(GSH)形式。抑制Pf中的这种酶会阻碍寄生虫生长。此外,已经证实PfGR与人类GR不同。因此,PfGR是抗疟药物开发的一个极佳靶点。开发了一种利用液相色谱 - 质谱联用的功能测定法,以特异性鉴定和评估PfGR的抑制剂。使用重组PfGR酶以及1,4 - 萘醌(1)作为参考化合物,4 - 硝基苯并噻二唑(2)和亚甲蓝(3)作为其他化合物,我们将与对照相比产生的GSH浓度进行定量,以确定这些化合物的抑制作用。我们的结果与文献中报道的一致:化合物1 - 3抑制PfGR的IC50值分别为2.71、8.38和19.23µm。日内和日间变异系数值较低(分别为3.1%和2.4%)表明该测定法具有良好的精密度。因此,该测定法可用于快速、准确地筛选PfGR的其他潜在抑制剂。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验