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预测对致癌激酶PAK1具有高结合亲和力的细胞毒性去硫酸化皂苷:一项体外和计算机模拟相结合的研究。

Cytotoxic Desulfated Saponin from Predicted to Have High Binding Affinity to the Oncogenic Kinase PAK1: A Combined In Vitro and In Silico Study.

作者信息

Shahinozzaman Md, Ishii Takahiro, Takano Ryo, Halim Mohammad A, Hossain Md Amzad, Tawata Shinkichi

机构信息

The United Graduate School of Agricultural Sciences, Kagoshima University, Korimoto 1-21-24, Kagoshima 890-0065, Japan.

PAK Research Center, University of the Ryukyus, Okinawa 903-0213, Japan.

出版信息

Sci Pharm. 2018 Aug 31;86(3):E32. doi: 10.3390/scipharm86030032.

Abstract

Sea cucumbers have long been utilized in foods and Asiatic folk medicines for their nutritive and health benefits. Herein, three sea cucumber species were investigated and showed the highest cytotoxicity among these. Next, a desulfated saponin, desulfated echinoside B (DEB), was purified from through bioassay-guided fractionation. LC-ESI-MS (Liquid chromatography-electrospray ionization mass spectrometry) analysis also showed to be a rich source of saponins. DEB showed cytotoxicity on cancer cells with IC values of 0.5⁻2.5 µM, and on brine shrimps with an IC value of 9.2 µM. In molecular docking studies, DEB was found to bind strongly with the catalytic domain of PAK1 (p21-activated kinase 1) and it showed binding energy of -8.2 kcal/mol compared to binding energy of -7.7 kcal/mol for frondoside A (FRA). Both of them bind to the novel allosteric site close to the ATP-binding cleft. Molecular dynamics (MD) simulation demonstrated that DEB can form a more stable complex with PAK1, remaining inside the allosteric binding pocket and forming the maximum number of hydrogen bonds with the surrounding residues. Moreover, important ligand binding residues were found to be less fluctuating in the DEB-PAK1 complex than in the FRA-PAK1 complex throughout MD simulation. Our experimental and computational studies showed that both DEB and FRA can act as natural allosteric PAK1 inhibitors and DEB appeared to be more promising than FRA.

摘要

海参长期以来因其营养和健康益处而被用于食品和亚洲民间药物中。在此,对三种海参进行了研究,它们在这些海参中表现出最高的细胞毒性。接下来,通过生物活性导向分级分离从[海参名称未给出]中纯化出一种去硫酸化皂苷,去硫酸化棘皮苷B(DEB)。液相色谱 - 电喷雾电离质谱(LC - ESI - MS)分析也表明[海参名称未给出]是皂苷的丰富来源。DEB对癌细胞的IC值为0.5⁻2.5 μM,对卤虫的IC值为9.2 μM,表现出细胞毒性。在分子对接研究中,发现DEB与PAK1(p21激活激酶1)的催化结构域强烈结合,与弗罗多苷A(FRA)的结合能 - 7.7 kcal/mol相比,其结合能为 - 8.2 kcal/mol。它们都结合到靠近ATP结合裂隙的新型变构位点。分子动力学(MD)模拟表明,DEB可以与PAK1形成更稳定的复合物,保留在变构结合口袋内,并与周围残基形成最大数量的氢键。此外,在整个MD模拟过程中,发现重要的配体结合残基在DEB - PAK1复合物中比在FRA - PAK1复合物中波动更小。我们的实验和计算研究表明,DEB和FRA都可以作为天然的变构PAK1抑制剂,并且DEB似乎比FRA更有前景。

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