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

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作者
Gazi, Inge [1 ,2 ]
Franc, Vojtech [1 ,2 ]
Tamara, Sem [1 ,2 ]
van Gool, Martine P. [3 ]
Huppertz, Thom [3 ,4 ]
Heck, Albert J.R. [1 ,2 ]
机构
[1] Biomolecular Mass Spectrometry and Proteomics, Bijvoet Centre for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Padualaan 8, CH, Utrecht,3584, Netherlands
[2] Netherlands Proteomics Centre, Padualaan 8, CH, Utrecht,3584, Netherlands
[3] FrieslandCampina, Stationsplein 4, LE, Amersfoort,3818, Netherlands
[4] Department of Agrotechnology and Food Sciences, Wageningen University, Bornse Weilanden 9, WG, Wageningen,6708, Netherlands
基金
荷兰研究理事会;
关键词
Bovine milk proteins - Controlled conditions - Glycation - Hotspots - LC-MS-MS - Powder production - Powder samples - Primary sequences - Protein sequences - Skim milk powder;
D O I
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学科分类号
摘要
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 hot-spots 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. © 2022 The Author(s)
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