1H-N.m.r. spectral assignments for two series of heparin-derived oligosaccharides

Abstract

Six heparin-derived oligosaccharides, ranging in size from di- to octa-saccharide and forming two closely related series different in structure by the substitution of an unsulfated d-glucuronate for a 2-sulfated l-iduronate residue, have been characterized by 2-dimensional 1H-n.m.r. spectroscopy. In addition to providing new data on hexa- and octa-saccharides, several important changes to previously published data have been found for the two tetrasaccharides. The d-glucuronic acid H-5 proton is assigned to a resonance in the same region as resonances for the H-3 and H-4 d-glucuronate protons, rather than downfield from these resonances as earlier reported. The presence of d-glucuronic acid in the heparin sequence of the series-1 fragments affects the positions of neighboring d-glucosamine resonances, in particular shifting the anomeric proton signal in the preceding d-glucosamin 0.1–0.2 p.p.m. downfield. Resonances from the reducing-end d-glucosamines differ from internal d-glucosamine resonances both in relative position and in the degree of chemical shift difference between the H-6 and H-6′ protons. This work illustrates the usefulness of two-dimensional techniques in determining heparin structure and emphasizes the need for direct analysis, rather than assignment by comparison to model compounds.