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Updated: Oct 13, 2026

Synthesis and Structure Determination of µ-Conotoxin PIIIA Isomers with Different Disulfide Connectivities
Published on: October 2, 2018
Structure, stability, and antioxidative mechanism of novel antioxidant peptides from Agaricus bisporus prepared by
Xuerui Wang1, Chun Qin1, Xia Ma1
1College of Food Science and Engineering, Gansu Agricultural University, Lanzhou, China.
Abstract:
Three novel antioxidant peptides (FPEF, LGFD, MGFGL, molecular weight <1000 Da) were isolated from Agaricus bisporus via sequential DA201-C macroporous resin, Sephadex G-100 gel filtration, and RP-HPLC. Molecular docking revealed strong Keap1 binding (energies: -8.2 to -8.7 kcal/mol) via hydrogen bonds and π-alkyl interactions. Cellular assays confirmed that all peptides alleviated H₂O₂-induced oxidative damage in HepG2 cells by reducing ROS/MDA levels, enhancing SOD/CAT/GSH-Px activities, and upregulating Nrf2-target genes (HO-1, NQO-1). Structural analysis indicated that FPEF's stability arose from balanced secondary structure and flexibility, rather than high ordered-structure content. FPEF exhibited superior stability under heat (100 °C), pH (3-11), and simulated gastrointestinal digestion (>90% retention), while MGFGL showed the highest ABTS radical scavenging activity (98.62% at 1.5 mg/mL). Collectively, FPEF shows promise as a natural antioxidant for functional food and nutricosmetic applications.

