Determination of the primary structures of heparin- and heparan sulfate-derived oligosaccharides using band-selective homonuclear-decoupled two dimensional H-1 NMR experiments
Wl. Chuang et al., Determination of the primary structures of heparin- and heparan sulfate-derived oligosaccharides using band-selective homonuclear-decoupled two dimensional H-1 NMR experiments, ANALYT CHEM, 73(10), 2001, pp. 2310-2316
Band-selective homonuclear-decoupled (BASHD) two-dimensional NMR experiment
s are applied to the assignment of H-1 NMR spectra of oligosaccharides, usi
ng as an example a heparin-derived hexasaccharide. The anomeric (H1) region
of the H-1 NMR spectrum is band-selected in the F-1 dimension. With the in
creased resolution that results from less truncation of interferograms in t
he t(1) dimension, finer digital resolution in the F-1 dimension, and colla
pse of multiplets to singlets in the F-1 dimension, cross-peaks to the anom
eric protons of the two iduronic acid residues, which overlap in normal two
-dimensional total correlation spectroscopy (TOCSY) and rotating frame Over
hauser enhancement spectroscopy (ROESY) spectra of the hexasaccharide, are
resolved in BASHD-TOCSY and BASHD-ROESY spectra, leading to an unequivocal
assignment of the H-1 NMR spectrum of the hexasaccharide. Incorporation of
the water attenuation by transverse relaxation method for the complete and
selective elimination of the water resonance into two-dimensional BASHD exp
eriments makes it possible to observe oligosaccharide resonances at the fre
quency of the water resonance, as demonstrated with the observation of cros
s-peaks to resonances at the frequency of the water resonance in BASHD-TOCS
Y spectra of a second heparin-derived hexasaccharide.