银杏
分子动力学
化学
范德瓦尔斯力
对接(动物)
IC50型
分子力学
生物化学
银杏
立体化学
计算化学
体外
药理学
分子
生物
有机化学
植物
医学
护理部
作者
Xiang Wang,Yejun Deng,Yang Zhang,Caihong Zhang,Lujie Liu,Yong Liu,Jianxin Jiang,Pujun Xie,Lixin Huang
标识
DOI:10.1021/acs.jafc.3c00826
摘要
Food-derived α-glucosidase inhibitory peptides have gained significant interest in treating type 2 diabetes mellitus (T2DM) owing to their favorable safety profiles. Molecular docking combined with molecular dynamics simulation was performed to screen α-glucosidase inhibitory peptides from Ginkgo biloba seed cake (GBSC), and two novel peptides (Met-Pro-Gly-Pro-Pro (MPGPP) and Phe-Ala-Pro-Ser-Trp (FAPSW)) were acquired. The results of molecular docking and molecular dynamics simulation suggested that FAPSW and MPGPP could generate stable complexes with 3wy1, and the electrostatic and van der Waals forces played contributory roles in FAPSW and MPGPP binding to 3wy1. The α-glucosidase inhibition assay corroborated that FAPSW and MPGPP had good α-glucosidase inhibition capacity, with IC50 values of 445.34 ± 49.48 and 1025.68 ± 140.78 μM, respectively. In vitro simulated digestion results demonstrated that FAPSW and MPGPP strongly resisted digestion. These findings lay a theoretical foundation for FAPSW and MPGPP in treating T2DM.
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