Hu Kaixuan, Sun Guangzhou, Yu Wentong, Zhang Mengyu, Wang Shuang, Cao Yujie, Hu Dongling, Liang Li, He Gang, Hu Jianping, Liu Wei
Bamboo & Forest Institute of Science, Technology and Industrial Innovation, Leshan Normal University, Leshan 614004, China.
Key Laboratory of Medicinal and Edible Plants Resources Development of Sichuan Education Department, School of Pharmacy, Chengdu University, Chengdu 610106, China.
Molecules. 2025 Jun 27;30(13):2774. doi: 10.3390/molecules30132774.
Umami is a fundamental taste sensation, often described as a delicious and pleasant flavor perception. To enhance or complement the original flavor and meet the tastes of diverse regions, umami dipeptides have been extensively utilized in global food manufacturing. Currently, the application and purification techniques of dipeptides are relatively mature, while their umami mechanisms and molecular modification are both scarce. In this work, the 3D structure of the umami dipeptide target T1R1/T1R3 was first obtained through sequence alignment and homology modeling, then followed by the successful construction of a database containing 400 samples of dipeptides. Subsequently, the complex models of T1R1/T1R3, respectively, with DG (Asp-Gly) and EK (Glu-Lys) (i.e., T1R1_DG/T1R3, T1R1/T1R3_DG, T1R1_EK/T1R3, and T1R1/T1R3_EK) were obtained via molecular docking and virtual screening. Finally, based on comparative molecular dynamics (MD) simulation trajectories, the binding free energy was calculated to investigate receptor-ligand recognition and conformational changes, providing some implications for potential modifications of umami dipeptides. T1R1 tends to bind relatively small umami dipeptides, whereas T1R3 does the opposite, both of which favor the recognition of acidic and hydrophilic dipeptides. By comparing strategies such as hydroxyl introduction and chain length alteration, electrostatic effects may be more important than non-polar effects in molecular design. This work not only explores the recognition mechanism of umami dipeptides with the receptor T1R1/T1R3 showing certain theoretical significance, but also provides feasible suggestions for dipeptide screening and modification having certain application value.
鲜味是一种基本的味觉感受,通常被描述为一种美味且宜人的风味感知。为了增强或补充原味并满足不同地区的口味需求,鲜味二肽已在全球食品制造中得到广泛应用。目前,二肽的应用和纯化技术相对成熟,而其鲜味机制和分子修饰方面的研究都较为匮乏。在这项工作中,首先通过序列比对和同源建模获得了鲜味二肽靶点T1R1/T1R3的三维结构,随后成功构建了一个包含400个二肽样本的数据库。接着,通过分子对接和虚拟筛选分别获得了T1R1/T1R3与DG(天冬氨酸-甘氨酸)和EK(谷氨酸-赖氨酸)的复合物模型(即T1R1_DG/T1R3、T1R1/T1R3_DG、T1R1_EK/T1R3和T1R1/T1R3_EK)。最后,基于比较分子动力学(MD)模拟轨迹计算结合自由能,以研究受体-配体识别和构象变化,为鲜味二肽的潜在修饰提供一些启示。T1R1倾向于结合相对较小的鲜味二肽,而T1R3则相反,两者都有利于识别酸性和亲水性二肽。通过比较诸如引入羟基和改变链长等策略,在分子设计中静电效应可能比非极性效应更为重要。这项工作不仅探索了鲜味二肽与受体T1R1/T1R3的识别机制,具有一定的理论意义,还为二肽筛选和修饰提供了可行的建议,具有一定的应用价值。