Structural and tribological studies on the interaction of porcine gastric mucin with non- and cationic-modified β-lactoglobulins.

Biolubrication Biotribology Cationization Mucin β-lactoglobulin

Journal

Colloids and surfaces. B, Biointerfaces
ISSN: 1873-4367
Titre abrégé: Colloids Surf B Biointerfaces
Pays: Netherlands
ID NLM: 9315133

Informations de publication

Date de publication:
21 Apr 2024
Historique:
received: 24 01 2024
revised: 16 04 2024
accepted: 19 04 2024
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 26 4 2024
Statut: aheadofprint

Résumé

β-lactoglobulin (BLG) is the major whey protein with negative charges at neutral pH in aqueous media. Thus, the interaction with mucins, the major polyanionic component of mucus, is very weak due to the electrostatic repulsion between them. The present study postulates that cationization of BLG molecules may reverse the interaction characteristics between BLG and mucin from repulsive to associative. To this end, cationic-modified BLGs were prepared by grafting positively charged ethylenediamine (EDA) moieties into the negatively charged carboxyl groups on the aspartic and glutamic acid residues and compared with non-modified BLG upon mixing with porcine gastric mucin (PGM). To characterize the structural and conformational features of PGM, non/cationized BLGs, and their mixtures, various spectroscopic approaches, including zeta potential, dynamic light scattering (DLS), and circular dichroism (CD) spectroscopy were employed. Importantly, we have taken surface adsorption with optical waveguide lightmode spectroscopy (OWLS), and tribological properties with pin-on-disk tribometry at the sliding interface as the key approaches to determine the interaction nature between them as mixing PGM with polycations can lead to synergistic lubrication at the nonpolar substrate in neutral aqueous media as a result of an electrostatic association. All the spectroscopic studies and a substantial improvement in lubricity collectively supported a tenacious and associative interaction between PGM and cationized BLGs, but not between PGM and non-modified BLG. This study demonstrates a unique and successful approach to intensify the interaction between BLG and mucins, which is meaningful for a broad range of disciplines, including food science, macromolecular interactions, and biolubrication etc.

Identifiants

pubmed: 38669751
pii: S0927-7765(24)00183-8
doi: 10.1016/j.colsurfb.2024.113924
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113924

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Hadi Asgharzadeh Shirazi (HA)

Department of Mechanical Engineering, Technical University of Denmark, DK-2800, Kgs. Lyngby, Denmark.

Seunghwan Lee (S)

Department of Mechanical Engineering, Technical University of Denmark, DK-2800, Kgs. Lyngby, Denmark; Institute of Functional Surfaces, School of Mechanical Engineering, University of Leeds, LS2 JT9, Leeds, The United Kingdom. Electronic address: S.Lee4@leeds.ac.uk.

Saif Ullah (S)

Department of Chemistry, Technical University of Denmark, DTU Chemistry, DK-2800, Kgs. Lyngby, Denmark.

Kristoffer Almdal (K)

Department of Chemistry, Technical University of Denmark, DTU Chemistry, DK-2800, Kgs. Lyngby, Denmark.

Classifications MeSH