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Updated: Aug 1, 2026

Peptide-based Identification of Functional Motifs and their Binding Partners
Published on: June 30, 2013
Unveiling dual-functional umami peptides with antioxidant effects from eggshell membrane byproducts: A machine
Lingjiao Zhu1, Jingyan Li1, Vincent Guyonnet2
1Hubei Key Laboratory for Processing and Transformation of Agricultural Products, College of Food Science and Engineering, Wuhan Polytechnic University, Wuhan 430023, China.
Abstract:
This study developed an efficient strategy for exploring novel dual-functional umami peptides with antioxidant activity from eggshell membrane (ESM), a protein-rich byproduct of the food industry, by integrating machine learning, molecular docking, molecular dynamics simulations, quantum chemistry and in vitro validations. Three novel peptides (CDDDF, WHDCHR, and CWDVYR) were identified from in silico ESM hydrolysates. The synthesized peptides exhibited pronounced umami taste with low recognition thresholds (0.04-0.10 mM), significant umami-enhancing effects, and potent free radical scavenging and reducing capacities. Quantum chemical analyses indicated that Cys, Asp, and Trp residues served as key active sites for both umami recognition and antioxidant activities. Molecular docking and dynamics simulations revealed that these peptides could stably bind to key amino acids in T1R1/T1R3 through hydrogen-bonding and hydrophobic interactions. This work provides robust guidance for discovering functional umami peptides from sustainable protein sources and offers novel insights into their structure-activity relationships and taster mechanisms.
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