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Zhipeng Yu

Researcher at Bohai University

Publications -  34
Citations -  764

Zhipeng Yu is an academic researcher from Bohai University. The author has contributed to research in topics: Peptide & Chemistry. The author has an hindex of 10, co-authored 34 publications receiving 344 citations. Previous affiliations of Zhipeng Yu include Beijing Technology and Business University.

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Intracellular ROS scavenging and antioxidant enzyme regulating capacities of corn gluten meal-derived antioxidant peptides in HepG2 cells.

TL;DR: Results suggested that both CPF1 and CPF2 exhibited positive effects on the activities of the intracellular antioxidant enzymes SOD, CAT and GR, as well as on the total GSH levels in HepG2 cells under conditions of oxidative stress.
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Preparation and identification of antioxidant peptides from cottonseed proteins

TL;DR: In this paper, the authors investigated the antioxidant properties of cottonseed peptides and found that the peptides prepared by enzymatic hydrolysis and microbial fermentation both showed antioxidant properties, and suggested that the antioxidant peptides from cottonseed protein had the potential as functional ingredients in foods.
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Novel membrane peptidase inhibitory peptides with activity against angiotensin converting enzyme and dipeptidyl peptidase IV identified from hen eggs

TL;DR: The ACE and DPP-IV inhibitory peptides identified from hen egg proteins can be used as functional food ingredients for controlling hypertension and diabetes.
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Digestion and absorption of an egg white ACE-inhibitory peptide in human intestinal Caco-2 cell monolayers.

TL;DR: The apparent permeability coefficients (Papp) of TNGIIR from the apical to basolateral side in Caco-2 cell monolayers was determined to be (4.92 ± 0.40) × 10−6 cm/s, indicating that TNG IIR can transport across CACs in intact form, and suggesting that the main transport route for TngIIR was paracellular pathway via TJs.
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Identification of tuna protein-derived peptides as potent SARS-CoV-2 inhibitors via molecular docking and molecular dynamic simulation.

TL;DR: Molecular docking analysis revealed that a potential antiviral peptide EEAGGATAAQIEM (E-M) could interact with residues Thr190, Thr25, Thr26, Ala191, Leu50, Met165, Gln189, Glu166, His164, His41, Cys145, Gly143, and Asn119 of Mpro via 11 conventional hydrogen bonds and one alkyl interaction.