Journal
CARBOHYDRATE RESEARCH
Volume 324, Issue 1, Pages 53-65Publisher
ELSEVIER SCI LTD
DOI: 10.1016/S0008-6215(99)00278-5
Keywords
C-13-labeling; conformation; NMR spectroscopy; octasaccharide; restrained molecular dynamics; Shigella dysenteriae type 1; simulated annealing; TOCSY; T-ROESY
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A synthetic octasaccharide fragment (2) of the O-specific polysaccharide (1) of Shigella dysenteriae type 1 has been studied as its methyl glycoside by one- and two-dimensional homo- and heteronuclear NMR spectroscopy. Complete H-1 and C-13 NMR assignments have been generated, and the C-13 spin-lattice relaxation times have been measured for the octasaccharide 2. A congener (6) of this octasaccharide containing one D-galactose residue with a specific C-13 label at C-1 has been synthesized and used to measure interglycosidic C-13-H-1 coupling by the 2D J-resolved H-1 NMR method. From the NMR data, three types of conformational restraints were developed: (a) 29 inter-residue, distance restraints; (b) 48 intra-residue, ring atom dihedral angle restraints, and (c) one heteronuclear, inter-residue dihedral angle restraint. The use of these restraints in a restrained molecular dynamics computation with simulated annealing yielded a conformation resembling a short, irregular spiral, with methyl substituents on the exterior. Published by Elsevier Science Ltd.
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