In Silico Docking Analysis of A-type Proanthocyanidins to α-Glucosidase Constructed by Correlation with in Vitro Bioassay

S. Ho, Yili Lin, Sheng-Fa Tsai, Shoei‐Sheng Lee
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引用次数: 1

Abstract

The type A proanthocyanidins (2−8) with (2β→O→7, 4β→8) interflavane linkage, isolated from Machilus philippinensis, have been found to possess inhibitory activity against α-glucosidase (EC 3.2.1.20 from Bacillus stearothermophilus). To rationalize such activity, computer assisted docking of these compounds and the positive control, acarbose, on the conformation model of α-glucosidase (AG), built by using human intestinal maltase glucoamylase as a template, was undertaken in this study. The result showed good correlation between IC50 values and docking scores, expressed as binding energy (ΔG), obtained from London (trimatch)-refinement (forcefield AffinityΔG) mode. Among these isolates, the most potent aesculitannin B (2) (IC50 3.5μM) showed the best docking score (ΔG -21.48 kcal/mol). Being interested in clarification of structure and activity relationship, virtual screening on the related compounds, including the de-unit III homologs of 2−8 (i.e., nor- series) and additional 13 stereoisomers of the trimeric 2 at the C-2 and C-3 positions of units II and III, was further carried out. This docking study indicated the de-unit III homologs of 2−8 did not have better binding energies than 2. As for the trimers, 3-entC, 3C-entE, 3ent-C, 3C, and 3ent, showed comparable docking score to 2. The verification of this virtual screening was partially done by evaluating the inhibitory activity of the dimeric 2-nor-ent, 3-nor, 3-nor-ent, and iso-2-nor-ent, isolated from peanut skins, against α-glucosidase. Of these, iso-2-nor-ent, the only proanthocyanidin with (2β→O→7, 4β→6) interflavane linkage, showed the best activity (IC50 9.72 μM). Their simulation profiles of docking score also displayed a reasonable qualitative consistency with the overall trend of the bioassay results. This study demonstrates that virtual screening using this built model to search α-glucosidase inhibitors is facile and feasible and peanut skin might be used as a hypoglycemic food.
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a型原花青素与α-葡萄糖苷酶的硅对接分析
具有(2β→O→7,4 β→8)黄烷连锁的A型原花青素(2−8)对嗜热脂肪芽孢杆菌α-葡萄糖苷酶(EC 3.2.1.20)具有抑制活性。为了使这种活性合理化,本研究以人肠道麦芽糖酶葡萄糖淀粉酶为模板构建了α-葡萄糖苷酶(AG)的构象模型,并将这些化合物与阳性对照阿卡波糖进行了计算机辅助对接。结果表明,IC50值与对接分数之间具有良好的相关性,对接分数表示为结合能(ΔG),由London (trimmatch)-refine (forcefield AffinityΔG)模式得到。其中,最有效的aesculitannin B (2) (IC50为3.5μM)的对接分数最高(ΔG -21.48 kcal/mol)。为了澄清结构和活性关系,进一步对相关化合物进行了虚拟筛选,包括2−8的去单元III同源物(即非-系列)和II和III单元C-2和C-3位置的三聚体2的另外13个立体异构体。该对接研究表明,2−8的脱单元III同源物的结合能并不比2好。三聚体中,3-entC、3C- ente、3ent- c、3C和3ent的对接评分为2分。通过评估从花生皮中分离的二聚体2-no -ent、3-nor、3-no -ent和异-2-no -ent对α-葡萄糖苷酶的抑制活性,部分验证了这种虚拟筛选。其中,唯一具有(2β→O→7,4 β→6)间烷连锁的原花青素异-2-no -ent活性最高(IC50为9.72 μM)。他们的对接评分模拟曲线也与生物测定结果的总体趋势表现出了合理的定性一致性。本研究表明,利用所建立的模型进行虚拟筛选寻找α-葡萄糖苷酶抑制剂是简单可行的,花生皮有可能作为一种降糖食品。
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