Domain mapping of chondroitin/dermatan sulfate glycosaminoglycans enables structural characterization of proteoglycans.

Of all post-translational modifications known, glycosaminoglycans (GAGs) remain one of the most challenging to study, and despite the recent years of advancement in MS technologies and bioinformatics, detailed knowledge about the complete structures of GAGs as part of proteoglycans (PGs) is limited. To address this issue, we have developed a protocol to study PG-derived GAGs. CS/DS conjugates from the rat insulinoma cell line, INS-1 832/13, known to produce primarily the PG chromogranin-A, were enriched by anion-exchange chromatography after pronase digestion. Following benzonase and hyaluronidase digestions, included in the sample preparation due to the apparent interference from oligonucleotides and hyaluronic acid in the analysis, the GAGs were orthogonally depolymerized and analyzed using nano-flow reversed-phase LC-MS/MS in negative mode. To facilitate the data interpretation, we applied an automated LC-MS peak detection and intensity measurement via the Proteome Discoverer software. This approach effectively provided a detailed structural description of the non-reducing end, internal, and linkage region domains of the CS/DS of chromogranin-A, the major PG produced by the INS-1 832/13 cells. The co-polymeric CS/DS GAGs constituted primarily consecutive glucuronic acid-containing disaccharide units, or CS motifs, of which the N-acetylgalactosamine residues were 4-O-sulfated, interspersed by single IdoA-containing disaccharide units. Our data suggest a certain heterogeneity of the GAGs due to the identification of, not only CS/DS GAGs, but also of GAGs entirely of CS character. The presented protocol allows for the detailed characterization of PG-derived GAGs, which may greatly increase the knowledge about GAG structures in general, and eventually lead to better understanding of how GAG structures are related to biological functions.