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通过虚拟筛选和生物测定研究发现天然 PI3Kδ 抑制剂。

Discovery of a natural PI3Kδ inhibitor through virtual screening and biological assay study.

机构信息

School of Traditional Chinese Medicine, Capital Medical University, Fengtai District, Beijing, 100069, PR China.

School of Traditional Chinese Medicine, Capital Medical University, Fengtai District, Beijing, 100069, PR China; Beijing Key Laboratory of Traditional Chinese Medicine Collateral Disease Theory Research, Capital Medical University, Fengtai District, Beijing, 100069, PR China.

出版信息

Biochem Biophys Res Commun. 2019 Jan 15;508(3):709-714. doi: 10.1016/j.bbrc.2018.12.009. Epub 2018 Dec 7.

Abstract

Phosphoinositide-3-kinase-δ (PI3Kδ) is a key regulator in the process of IgE mediated mast cell degranulation, which directly induces allergic diseases, such as asthma. This study is aimed at discovery of natural PI3Kδ inhibitors from Chinese medicine and evaluating their anti-mast cell degranulation activity. A combined virtual screening based on 3D pharmacophore model and molecular docking was used to screen for bioactive ingredients directly targeting PI3Kδ. Then, an in vitro kinase inhibition assay was conducted to evaluate the PI3Kδ inhibitory activity of the virtual screening hits. Subsequently, a β-hexosaminidase release assay was performed to verify the anti-mast cell degranulation activity of the active compounds. Finally, ginkgoneolic acid was identified as a PI3Kδ inhibitor (IC = 2.49 μM) and exhibited anti-mast cell degranulation activity in vitro (IC = 2.40 μM). Docking studies showed that Glu826, Val827 and Val828 were key amino acid residues for PI3Kδ inhibitory activity. Ginkgoneolic acid may be a potential lead compound for developing effective and safe PI3Kδ-inhibiting drugs.

摘要

磷酸肌醇 3-激酶-δ(PI3Kδ)是 IgE 介导的肥大细胞脱颗粒过程中的关键调节剂,它直接诱导哮喘等过敏性疾病。本研究旨在从中药中发现天然的 PI3Kδ 抑制剂,并评估其抗肥大细胞脱颗粒活性。采用基于 3D 药效团模型和分子对接的组合虚拟筛选方法,直接针对 PI3Kδ 筛选生物活性成分。然后,进行体外激酶抑制测定以评估虚拟筛选命中物对 PI3Kδ 的抑制活性。随后,进行β-己糖胺酶释放测定以验证活性化合物的抗肥大细胞脱颗粒活性。最后,鉴定银杏酸为 PI3Kδ 抑制剂(IC=2.49 μM),并在体外显示抗肥大细胞脱颗粒活性(IC=2.40 μM)。对接研究表明,Glu826、Val827 和 Val828 是 PI3Kδ 抑制活性的关键氨基酸残基。银杏酸可能是开发有效和安全的 PI3Kδ 抑制药物的潜在先导化合物。

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