Identification, in silico selection, and mechanism study of novel antioxidant peptides derived from the rice bran protein hydrolysates

Food Chem. 2023 May 15:408:135230. doi: 10.1016/j.foodchem.2022.135230. Epub 2022 Dec 16.

Abstract

The work aimed to assess the antioxidant ability and obtain a new antioxidant peptide from rice bran protein. Rice bran protein was hydrolyzed by Alcalase, Neutral, Pepsin, Chymotrypsin, and Trypsin, separately. Trypsin hydrolysate (T-RBPH) showed high Fe2+ chelating activity (IC50, 2.271 ± 0.007 mg/mL), DPPH and hydroxyl radical scavenging ability (IC50, 0.191 ± 0.006 and 1.038 ± 0.034 mg/mL). Moreover, T-RBPH could alleviate the H2O2-induced oxidative damage in Caco-2. The T-RBPH was purified and identified by UF, GF, FPLC, and LC-MS/MS. Finally, 9-amino acid peptide-AFDEGPWPK with low molecular weight (1045.48 Da), high antioxidant activity, good safety, and solubility was screened by in silico method and chemical oxidation determination, and its interaction with Keap1 was also demonstrated. The ORAC and DPPH radical scavenging ability of AFDEGPWPK were 44.16 ± 0.79 and 28.38 ± 0.14 μmol TE/mM. Moreover, the Molecular docking and Western blot (WB) results showed that AFDEGPWPK could enter the binding pocket in the Kelch domain and activate Keap1/Nrf2/HO-1 pathway.

Keywords: Antioxidant activity; Identification; In silicoprediction; Molecular docking; Purification; Rice bran protein hydrolysates.

MeSH terms

  • Antioxidants* / chemistry
  • Antioxidants* / pharmacology
  • Caco-2 Cells
  • Chromatography, Liquid
  • Humans
  • Hydrogen Peroxide / metabolism
  • Kelch-Like ECH-Associated Protein 1 / metabolism
  • Molecular Docking Simulation
  • NF-E2-Related Factor 2 / metabolism
  • Oryza* / chemistry
  • Peptides / chemistry
  • Protein Hydrolysates / chemistry
  • Tandem Mass Spectrometry
  • Trypsin / metabolism

Substances

  • Antioxidants
  • Protein Hydrolysates
  • Kelch-Like ECH-Associated Protein 1
  • Trypsin
  • Hydrogen Peroxide
  • NF-E2-Related Factor 2
  • Peptides