Wang Peng, Li Jun, Yi Hongbo, Zhu Danshi, Wang Shengnan, Zhang Na, Guo Xiaofei, Liu He
College of Food Science and Technology, Bohai, University, Jinzhou, LiaoNing 121010, China.
Harbin University of Commerce School of Food Engineering, Harbin, Heilongjiang, China.
Food Funct. 2025 May 19;16(10):3934-3948. doi: 10.1039/d4fo05274a.
In order to reduce the use of traditional salt (NaCl), this study aimed to rapidly identify novel peptides with salt-reducing effects from peanut protein. Four potential peptides were identified through virtual screening and molecular docking. The sensory evaluation and electronic tongue confirmed that the peptides SPDIY, DPSPR, QPGDY, and SPPGER had significant saltiness-enhancing effects, with saltiness enhancement thresholds ranging from 0.16 to 0.64 mmol L. Among them, DPSPR exhibited the most pronounced effect in enhancing saltiness, capable of replacing approximately 56.7% of NaCl. Molecular docking and dynamics simulation studies indicated that amino acid residues Arg272, Glu161, Gln279, Arg168, and Ser165 were found to play key roles in ligand-receptor binding. Additionally, antioxidant activity assays demonstrated that the peptide QPGDY contributed to free radical scavenging in a dose-dependent manner through the hydrogen atom transfer mechanism. The combination of virtual screening technology and experimental validation greatly improved the efficiency and accuracy of peptide discovery and functional characterization, offering a promising strategy for the development of low-sodium foods with antioxidant properties.
为了减少传统食盐(氯化钠)的使用,本研究旨在从花生蛋白中快速鉴定出具有减盐效果的新型肽。通过虚拟筛选和分子对接鉴定出四种潜在肽。感官评价和电子舌证实,肽SPDIY、DPSPR、QPGDY和SPPGER具有显著的增咸效果,增咸阈值范围为0.16至0.64 mmol/L。其中,DPSPR在增强咸味方面表现出最显著的效果,能够替代约56.7%的氯化钠。分子对接和动力学模拟研究表明,发现氨基酸残基Arg272、Glu161、Gln279、Arg168和Ser165在配体-受体结合中起关键作用。此外,抗氧化活性测定表明,肽QPGDY通过氢原子转移机制以剂量依赖方式促进自由基清除。虚拟筛选技术与实验验证相结合,大大提高了肽发现和功能表征的效率和准确性,为开发具有抗氧化特性的低钠食品提供了一种有前景的策略。