Jilin Provincial Key Laboratory of Nutrition and Functional Food, College of Food Science and Engineering, Jilin University, Changchun 130062, China.
State Key Laboratory of Tea Plant Biology and Utilization, School of Tea and Food Science and Technology, Anhui Agricultural University, Hefei 230036, China.
Int J Mol Sci. 2022 Nov 3;23(21):13471. doi: 10.3390/ijms232113471.
Food-derived tripeptides can relieve colitis symptoms; however, their alleviation mode has not been systematically evaluated as an alternative nutritional compound. This study aimed to reveal the potential mechanism of 8000 food-derived tripeptides against acute colitis using a computer-aided screening strategy. Forty-one potential hub targets related to colitis with a Fit score > 4.0 were screened to construct the protein-protein and protein-tripeptide network based on the PharmMapper database and STRING software (Ver. 11.5). In addition, 30 significant KEGG signaling pathways with p-values < 0.001 that the 41 hub targets mainly participated in were identified using DAVID software (Ver. 6.8), including inflammatory, immunomodulatory, and cell proliferation and differentiation-related signaling pathways, particularly in the Ras- and PI3K-Akt signaling pathways. Furthermore, molecular docking was performed using the Autodock against majorly targeted proteins (AKT1, EGFR, and MMP9) with the selected 52 tripeptides. The interaction model between tripeptides and targets was mainly hydrogen-bonding and hydrophobic interactions, and most of the binding energy of the tripeptide target was less than −7.13 kcal/mol. This work can provide valuable insight for exploring food-derived tripeptide mechanisms and therapeutic indications.
食源性三肽可缓解结肠炎症状;然而,作为一种替代营养化合物,其缓解模式尚未得到系统评价。本研究旨在采用计算机辅助筛选策略,揭示 8000 种食源性三肽对抗急性结肠炎的潜在机制。基于 PharmMapper 数据库和 STRING 软件(Ver.11.5),筛选出 41 个与结肠炎相关的潜在关键靶点,Fit 评分>4.0,构建蛋白质-蛋白质和蛋白质-三肽网络。此外,使用 DAVID 软件(Ver.6.8)鉴定了 30 个显著的 KEGG 信号通路,p 值<0.001,41 个关键靶点主要参与其中,包括炎症、免疫调节和细胞增殖分化相关信号通路,特别是 Ras 和 PI3K-Akt 信号通路。此外,利用 Autodock 对主要靶向蛋白(AKT1、EGFR 和 MMP9)与选定的 52 种三肽进行分子对接。三肽与靶蛋白的相互作用模型主要为氢键和疏水相互作用,大多数三肽靶蛋白的结合能小于-7.13 kcal/mol。这项工作可以为探索食源性三肽的机制和治疗适应症提供有价值的见解。