没食子儿茶素没食子酸酯作为天然DPP-IV抑制剂的对接研究

Satish Kumar, Rajeev K. Singla, A. Garg
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引用次数: 1

摘要

DPP-IV酶是抗糖尿病药物的重要靶点之一。表没食子儿茶素没食子酸酯(EGCG)等天然产物已被报道通过多种机制具有抗糖尿病作用,其中包括抑制DPP-IV酶。然而,对其作用于DPP-IV酶的机制和作用部位尚未深入探讨。因此,本研究旨在使用VLife MDS 4.6进行EGCG与DPP-IV酶(PDB ID: 2P8S)的对接研究。结果表明,EGCG在DPP-IV酶上成功对接,对接评分为-87.584,而标准共结晶药物(环己胺抑制剂)的对接评分为-84.0564。进一步的相互作用分析表明,表没食子儿茶素没食子酸酯与Phe357A有芳香相互作用,与Arg125A、Glu206A和Arg358A有氢键作用。因此,基于目前的研究,表没食子儿茶素没食子酸酯可以进一步加工用于定制和设计新的DPP-IV抑制剂。
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Docking Studies of Epigallocatechin Gallate as Natural DPP-IV Inhibitor
DPP-IV enzyme is one of the important targets for the anti-diabetic drugs. Natural products like Epigallocatechin Gallate (EGCG) had been reported to have antidiabetic action vide multiple mechanisms which also includes inhibition of DPP-IV enzyme. However, its mechanism and site of action on DPP-IV enzyme was not thoroughly explored. Thus, the current study was aimed to perform docking studies of EGCG with the DPP-IV enzyme, (PDB ID: 2P8S) using VLife MDS 4.6. Results indicated that EGCG was successfully docked in the DPP-IV enzyme with dock score of -87.584 when compared with standard and co-crystallized drug (cyclohexalamine inhibitor) which has dock score of -84.0564. Further interaction analysis suggested that Epigallocatechin Gallate has aromatic interactions with Phe357A and hydrogen bonding with Arg125A, Glu206A and Arg358A. So based on the current study, Epigallocatechin Gallate can be further processed for tailoring and designing of novel DPP-IV inhibitors.
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