A multi-approach peptidomic analysis of hen egg white reveals novel putative bioactive molecules

被引:18
|
作者
Arena, Simona [1 ]
Renzone, Giovanni [1 ]
Scaloni, Andrea [1 ]
机构
[1] CNR, Prote & Mass Spectrometry Lab, ISPAAM, Via Argine 1085, I-80147 Naples, Italy
关键词
Egg white; Peptidomics; Bioactive molecules; ENZYME INHIBITORY PEPTIDES; GASTROINTESTINAL DIGESTION; ANTIHYPERTENSIVE PEPTIDES; ANTIOXIDANT PEPTIDES; PROTEINS; IDENTIFICATION; PURIFICATION; MEAT;
D O I
10.1016/j.jprot.2020.103646
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chicken egg white is a raw material broadly used as additive for the preparation of food and cosmetoceutical products. To describe its molecular properties, various proteomic investigations were performed in the last decade characterizing highly abundant components. No peptidomic counterparts were accomplished so far; scientific literature only reports on the characterization of specific bioactive peptides or preparations from egg white and its hydrolysates, which was performed through dedicated functional assays. In this study, a broad description of the egg white peptidome at 24, 336 and 672 h after laying was achieved using three peptide extraction procedures, which were combined with MALDI-TOF-TOF-MS and nanoLC-ESI-Q-Orbitrap-MS/MS analyses. In the whole, 506 peptides were characterized; they mostly resulted from the physiological degradation of intact proteins following the activity of endoprotease ArgC-, trypsin- and plasmin-like enzymes. Eventual detection of peptide post-translational modifications also provided structural information on parental proteins. When analyzed by bioinformatics and/or compared with literature data, identified peptides allowed recognizing a number of protein fragments associated with different hypothetical biological activities. These results confirmed previous observations regarding functional characteristics of egg white unfractionated preparations or purified molecules, emphasizing the useful application of this raw material in human nutrition and cosmetics. Finally, a comparative label-free peptidomic evaluation of samples stored for different times under refrigeration identified 31 peptides showing significant quantitative changes during storage. Biological significance: This study provided the largest inventory of peptides described in chicken egg while so far. In addition, it identified a number of protein fragments associated with hypothetical antihypertensive, antioxidant, antiinflammatory, antimicrobial, anticancer, antiviral, antibiofilm, calcium-binding, antidiabetic, antithrombotic, adipogenic differentiating, stimulating/immunostimulating, hormonal, lipid-binding and cell adhesion-affecting activities. These results confirmed previous observations regarding functional characteristics of egg white unfractionated preparations or purified molecules, emphasizing the useful application of this raw material in human nutrition and cosmetics.
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页数:10
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