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Identifying glycation hot-spots in bovine milk proteins during production and storage of skim milk powder

  • FrieslandCampina
  • Wageningen University & Research

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We investigated protein glycation in a complex milk system under controlled conditions representative of real-life consumer products, analysing intermediate and final products from skim milk powder production, and aged powder samples. We combined protein-centric LC-MS(/MS) with peptide-centric multi-protease LC-MS/MS focusing on the six most abundant bovine milk proteins. This strategy resulted in the identification of glycated proteoforms and of the extent of glycation per protein, high protein sequence coverage, and identification and relative occupancy of the glycation sites. We identified new glycation hotspots additionally to the ones already described in literature. Primary sequence motif analysis revealed that glycation hot-spots were preceded N-terminally by a stretch rich in basic amino acids, and followed C-terminally by a stretch enriched in aliphatic and hydrophobic amino acids. Our study considerably extends the current understanding of milk protein glycation, discussing glycation hot spots and their localisation in relation to the primary sequences and higher-order protein structures. (C)& nbsp;2022 The Author(s). Published by Elsevier Ltd.& nbsp;
Original languageEnglish
Article number105340
Pages (from-to)1-10
Number of pages10
JournalInternational Dairy Journal
Volume129
DOIs
Publication statusPublished - Jun 2022

Bibliographical note

Funding Information:
We acknowledge support from the Dutch Research Council (NWO) in the framework of the Innovation Fund for Chemistry (SATIN project 731.017.202). We thank Max Hoek (Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University; Netherlands Proteomics Centre) for assistance with the analysis of the glycation motif in the primary sequence of the proteins. We thank Kelly A. Dingess (Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University; Netherlands Proteomics Centre) for proofreading the manuscript.

Funding Information:
We acknowledge support from the Dutch Research Council (NWO) in the framework of the Innovation Fund for Chemistry (SATIN project 731.017.202 ). We thank Max Hoek ( Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University ; Netherlands Proteomics Centre ) for assistance with the analysis of the glycation motif in the primary sequence of the proteins. We thank Kelly A. Dingess (Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University; Netherlands Proteomics Centre) for proofreading the manuscript.

Publisher Copyright:
© 2022 The Author(s)

Funding

We acknowledge support from the Dutch Research Council (NWO) in the framework of the Innovation Fund for Chemistry (SATIN project 731.017.202). We thank Max Hoek (Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University; Netherlands Proteomics Centre) for assistance with the analysis of the glycation motif in the primary sequence of the proteins. We thank Kelly A. Dingess (Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University; Netherlands Proteomics Centre) for proofreading the manuscript. We acknowledge support from the Dutch Research Council (NWO) in the framework of the Innovation Fund for Chemistry (SATIN project 731.017.202 ). We thank Max Hoek ( Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University ; Netherlands Proteomics Centre ) for assistance with the analysis of the glycation motif in the primary sequence of the proteins. We thank Kelly A. Dingess (Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University; Netherlands Proteomics Centre) for proofreading the manuscript.

Keywords

  • Maillard induced glycation
  • Beta-lactoglobulin
  • Mass-spectrometry
  • Alpha-lactalbumin
  • Dairy-products
  • Water activity
  • Cows milk
  • Identification
  • Lactosylation
  • Nomenclature

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