偶氮染料对巴西副球虫氯酸酯合成酶抑制性能的研究。

IF 5.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Enzyme Inhibition and Medicinal Chemistry Pub Date : 2024-12-01 Epub Date: 2024-12-10 DOI:10.1080/14756366.2024.2427175
Katharina Fuchs, Massimo G Totaro, Marina Toplak, Aleksandar Bijelic, Peter Macheroux
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引用次数: 0

摘要

广谱除草剂草甘膦对5-烯醇丙酮酰莽草酸-3-磷酸合成酶(EPSPS)的有效抑制验证了莽草酸途径是开发抗菌、杀菌剂和除草剂的一个有前景的靶点。该途径的最后一种酶,choris酸合成酶(CS),催化一种不寻常的反应,使其成为新型抑制剂的一个有吸引力的靶点。因此,我们测试了一系列偶氮染料对致病真菌巴西副球虫(paracoccidiides brasiliensis, PbCS) CS的抑制潜力,并鉴定出偶氮染料PH011669的解离(Kd)和50%抑制常数(IC50)分别为1.1±0.1和10±1µM。分子对接和MD模拟提供了对抑制模式的深入了解,表明PH011669主要通过静电相互作用与酶的活性位点结合。因此,我们的研究首次将结构和计算方法结合起来,指导未来设计下一代CS抑制剂的工作。
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Investigation of the inhibitory properties of azo-dyes on chorismate synthase from Paracoccidioides brasiliensis.

The efficient inhibition of 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) by the broad-spectrum herbicide glyphosate validates the shikimate pathway as a promising target for developing antimicrobial, fungicidal and herbicidal agents. The last enzyme of this pathway, chorismate synthase (CS), catalyses an unusual reaction, making it an attractive target for novel inhibitors. Therefore, we tested a series of azo-dyes for their inhibitory potential against CS from the pathogenic fungus Paracoccidioides brasiliensis (PbCS) and identified the azo-dye PH011669 that exhibits a dissociation (Kd) and 50% inhibitory constant (IC50) of 1.1 ± 0.1 and 10 ± 1 µM, respectively. Molecular docking and MD simulations provided insight into the mode of inhibition, showing that PH011669 binds to the enzyme's active site primarily through electrostatic interactions. Thus, our study is the first to integrate structural and computational methods to guide future efforts towards designing the next generation of CS inhibitors.

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来源期刊
CiteScore
10.30
自引率
10.70%
发文量
195
审稿时长
4-8 weeks
期刊介绍: Journal of Enzyme Inhibition and Medicinal Chemistry publishes open access research on enzyme inhibitors, inhibitory processes, and agonist/antagonist receptor interactions in the development of medicinal and anti-cancer agents. Journal of Enzyme Inhibition and Medicinal Chemistry aims to provide an international and interdisciplinary platform for the latest findings in enzyme inhibition research. The journal’s focus includes current developments in: Enzymology; Cell biology; Chemical biology; Microbiology; Physiology; Pharmacology leading to drug design; Molecular recognition processes; Distribution and metabolism of biologically active compounds.
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