Glycoproteomics of milk: differences in sugar epitopes on human and bovine milk fat globule membranes
Wilson, Nicole L.
Robinson, Leanne J.
Packer, Nicolle H.
Karlsson, Niclas G.
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Wilson, Nicole L. Robinson, Leanne J.; Donnet, Anne; Bovetto, Lionel; Packer, Nicolle H.; Karlsson, Niclas G. (2008). Glycoproteomics of milk: differences in sugar epitopes on human and bovine milk fat globule membranes. Journal of Proteome Research 7 (9), 3687-3696
Oligosaccharides from human and bovine milk fat globule membranes were analyzed by LC-MS and LC-MS/MS. Global release of N-linked and O-linked oligosaccharides showed both to be highly sialylated, with bovine peak-lactating milk O-linked oligosaccharides presenting as mono- and disialylated core 1 oligosaccharides (Gal beta 1-3GalNAcol), while human milk had core type 2 oligosaccharides (Gal beta 1-3(GlcNAc beta 1-6) GalNAcol) with sialylation on the C-3 branch. The C-6 branch of these structures was extended with branched and unbranched N-acetyllactosamine units terminating in blood group H and Lewis type epitopes. These epitopes were also presented on the reducing terminus of the human, but not the bovine, N-linked oligosaccharides. The O-linked structures were found to be attached to the high molecular mass mucins isolated by agarose-polyacrylamide composite gel electrophoresis, where MUC1 and MUC4 were present. Analysis of bovine colostrum showed that O-linked core 2 oligosaccharides are present at the early stage (3 days after birth) but are down-regulated as lactation develops. This data indicates that human milk may provide different innate immune protection against pathogens compared to bovine milk, as evidenced by the presence of Lewis b epitope, a target for the Helicobacter pylori bacteria, on human, but not bovine, milk fat globule membrane mucins. In addition, non-mucin-type O-linked fucosylated oligosaccharides were found (NeuAc-Gal-GlcNAc1-3Fuc-ol in bovine milk and Gal-GlcNAc1-3Fuc-ol in human milk). The O-linked fucose structure in human milk is the first to our knowledge to be found on high molecular mass mucin-type molecules.