L. Poppe et al., THE SOLUTION CONFORMATION OF SIALYL-ALPHA(2-]6)-LACTOSE STUDIED BY MODERN NMR TECHNIQUES AND MONTE-CARLO SIMULATIONS, Journal of biomolecular NMR, 2(2), 1992, pp. 109-136
We present a comprehensive strategy for detailed characterization of t
he solution conformations of oligosaccharides by NMR spectroscopy and
force-field calculations. Our experimental strategy generates a number
of interglycosidic spatial constraints that is sufficiently large to
allow us to determine glycosidic linkage conformations with a precisio
n heretofore unachievable. In addition to the commonly used {H-1,H-1}
NOE contacts between aliphatic protons, our constraints are: (a) homon
uclear NOEs of hydroxyl protons in H2O to other protons in the oligosa
ccharide, (b) heteronuclear {H-1,C-13} NOEs, (c) isotope effects of (O
H)-H-1/(OH)-H-2 hydroxyl groups on C-13 chemical shifts, and (d) long-
range heteronuclear scalar couplings across glycosidic bonds. We have
used this approach to study the trisaccharide sialyl-alpha(2 --> 6)-la
ctose in aqueous solution. The experimentally determined geometrical c
onstraints were compared to results obtained from force-field calculat
ions based on Metropolis Monte Carlo simulations. The molecule was fou
nd to exist in 2 families of conformers. The preferred conformations o
f the alpha(2 --> 6)-linkage of the trisaccharide are best described b
y an equilibrium of 2 conformers with PHI-angles at -60-degrees or 180
-degrees and of the 3 staggered rotamers of the OMEGA-angle with a pre
dominant gt conformer. Three intramolecular hydrogen bonds, involving
the hydroxyl protons on C8 and C7 of the sialic acid residue and on C3
of the reducing-end glucose residue, contribute significantly to the
conformational stability of the trisaccharide in aqueous solution.