has been established for the determination of uronate residues in glycosaminoglycans (GAGs) such as dermatan sulfate (DS), heparin (HP), and heparan sulfate (HS). Because of variation in the sulfonation positions in DS, HP, or HS, interpretation of spectra is difficult. Solvolysis was applied to rem
“Linkage Region” Sequences of Heparins and Heparan Sulfates: Detection and Quantification by Nuclear Magnetic Resonance Spectroscopy
✍ Scribed by M. Iacomini; B. Casu; M. Guerrini; A. Naggi; A. Pirola; G. Torri
- Book ID
- 102559886
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 117 KB
- Volume
- 274
- Category
- Article
- ISSN
- 0003-2697
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✦ Synopsis
The 13 C NMR spectra of most heparin and heparan sulfate preparations display minor signals not attributable to the glycosaminoglycan chains of these polysaccharides. These signals have been "concentrated" in oligosaccharides isolated from an acid hydrolyzate of heparin and shown to arise from the sequence GlcA-Gal-Gal-Xyl of the "linkage region" (LR) connecting the carbohydrate chains to the peptide chains in the original proteoglycans. Mono-and two-dimensional 1 H and 13 C NMR analysis of the major oligosaccharide (LR-OLIGO) indicated the prevalent structure GlcA-GlcNAc-GlcA-Gal-Gal-Xyl, where GlcNAc is partially 6-O-sulfated. 13 C NMR signals at 84.6 and 85.0 ppm, arising from C-3 of the two Gal residues, lend themselves to easy detection and quantification of the linkage region in heparins and heparan sulfates and can be used to assess the importance of the LR in the modulation of various biological activities of these glycosaminoglycans.
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