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采用超滤 LC-MS 结合酶通道阻断法筛选菊花中黄嘌呤氧化酶的选择性抑制剂。

Screening for selective inhibitors of xanthine oxidase from Flos Chrysanthemum using ultrafiltration LC-MS combined with enzyme channel blocking.

机构信息

State Key Laboratory of Natural Medicines (China Pharmaceutical University) , No. 24, Tongjia Lane, Jiangsu, Nanjing 210009, China.

State Key Laboratory of Natural Medicines (China Pharmaceutical University) , No. 24, Tongjia Lane, Jiangsu, Nanjing 210009, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Jun 15;961:56-61. doi: 10.1016/j.jchromb.2014.05.001. Epub 2014 May 14.

Abstract

In this study, a new method based on ultrafiltration liquid chromatography-mass spectrometry (UF-LC-MS) combined with enzyme channel blocking (ECB) was developed to discover bioactive components from herbal medicines. Xanthine oxidase (XOD), a critical enzyme for treating gout, was employed as the target protein for screening. By comparing chromatographic profiles of the compounds binding to XOD before and after the ECB experiment, the selective ligands could be distinguished from the non-selective binders. In this experiment, febuxostat bound to the channel entering into the active site of the enzyme and prevented potential ligands from binding. Finally, four compounds, namely, luteolin-7-O-glucoside, apigenin-7-O-glucoside, luteolin and apigenin were screened and identified as the candidate XOD inhibitors based on the ultrafiltration chromatogram of Flos Chrysanthemum, a famous traditional Chinese medicine used in many prescriptions for gout treatment. To verify the compounds screened further, a microplate method was applied to evaluate their enzyme inhibitory activities. The IC50 values of the above 4 compounds were 23.61, 38.80, 1.54 and 1.96μM, respectively. The structure-function relationship was also estimated according to the in vitro assay. The results were in favor of the hypothesis that the Flos Chrysanthemum extract might be used for gout treatment by inhibiting XOD.

摘要

在这项研究中,开发了一种基于超滤液相色谱-质谱联用(UF-LC-MS)结合酶通道阻断(ECB)的新方法,用于从草药中发现生物活性成分。黄嘌呤氧化酶(XOD)是治疗痛风的关键酶,被用作筛选的靶蛋白。通过比较 XOD 结合化合物在 ECB 实验前后的色谱图谱,可以将选择性配体与非选择性配体区分开来。在这项实验中,非布司他结合到进入酶活性位点的通道中,阻止潜在的配体结合。最后,根据菊花的超滤色谱图,筛选并鉴定了四种化合物,即木犀草素-7-O-葡萄糖苷、芹菜素-7-O-葡萄糖苷、木犀草素和芹菜素,作为候选 XOD 抑制剂。菊花是许多用于治疗痛风的处方中的一种中药。为了进一步验证筛选出的化合物,应用微孔板法评估了它们的酶抑制活性。上述 4 种化合物的 IC50 值分别为 23.61、38.80、1.54 和 1.96μM。根据体外测定还估计了结构-功能关系。结果支持菊花提取物通过抑制 XOD 用于治疗痛风的假设。

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