Identification of the Bioavailable Peptidome of Chia Protein Hydrolysate and the In Silico Evaluation of Its Antioxidant and ACE Inhibitory Potential [Dataset]

The incorporation of novel, functional, and sustainable foods in human diets is increasing because of their beneficial effects and environmental-friendly nature. Chia (Salvia hispanica L.) has proved to be a suitable source of bioactive peptides via enzymatic hydrolysis. These peptides could be resp...

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Bibliographic Details
Authors: Villanueva, Álvaro, Rivero-Pino, Fernando, Martín-Rubio, María E., González-de la Rosa, Teresa, Montserrat-de la Paz, Sergio, Millán-Linares, María del Carmen
Format: conjunto de datos
Publication Date:2024
Country:España
Institution:Consejo Superior de Investigaciones Científicas (CSIC)
Repository:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/360550
Online Access:http://hdl.handle.net/10261/360550
Access Level:Open access
Keyword:Beneficial effects
Absorption model
Higher statistical significance
Ace inhibitory potential
Ace inhibitor activity
2 cell culture
Molecular weight lower
20 unique peptides
Chia protein hydrolysates
Bioavailable peptides contained
Chia protein hydrolysate
Molecular features
Hydrolysate obtained
Bioavailable peptidome
Peptides could
Peptides agdahwty
Characterized peptides
Transwell system
Target organ
Sustainable foods
Suitable source
Silico tools
Silico evaluation
Results obtained
Identified using
Human diets
Friendly nature
Demonstrated bioactivity
Description
Summary:The incorporation of novel, functional, and sustainable foods in human diets is increasing because of their beneficial effects and environmental-friendly nature. Chia (Salvia hispanica L.) has proved to be a suitable source of bioactive peptides via enzymatic hydrolysis. These peptides could be responsible for modulating several physiological processes if able to reach the target organ. The bioavailable peptides contained in a hydrolysate obtained with Alcalase, as functional foods, were identified using a transwell system with Caco-2 cell culture as the absorption model. Furthermore, 20 unique peptides with a molecular weight lower than 1000 Da and the higher statistical significance of the peptide-precursor spectrum match (−10 log P) were assessed by in silico tools to suggest which peptides could be those exerting the demonstrated bioactivity. From the characterized peptides, considering the molecular features and the results obtained, the peptides AGDAHWTY, VDAHPIKAM, PNYHPNPR, and ALPPGAVHW are anticipated to be contributing to the antioxidant and/or ACE inhibitor activity of the chia protein hydrolysates.