Premium
Molecular dynamics simulation and nmr study of a blood group H trisaccharide
Author(s) -
Widmalm Göran,
Venable Richard M.
Publication year - 1994
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.360340811
Subject(s) - chemistry , trisaccharide , molecular dynamics , dielectric , dihedral angle , crystallography , conformational isomerism , nuclear overhauser effect , nuclear magnetic resonance spectroscopy , aqueous solution , stereochemistry , molecule , computational chemistry , physics , organic chemistry , hydrogen bond , optoelectronics
Abstract Molecular dynamics simulations in vacuum and solution have been carried out on 2′‐α‐ L ‐fucosyllactitol, a model for blood group H in conjunction with two‐dimensional nmr measurements on the same compound. Three independent starting conformations for the dynamics were chosen from low energy conformations obtained by a ϕ/ψ grid search. Nine 5 ns vacuum simulations of the trisaccharide were performed, employing three different ways to treat electrostatic interactions for each starting conformation: distance‐dependent dielectric with ε = r , constant dielectric with ε = 1, or constant dielectric with ε = 80. In vacuum, transitions of ϕ and ψ for the α‐ L ‐Fuc‐(1 → 2)‐β‐ D ‐Gal element occur in a cooperative manner. The virtual distance obtained for H1 in fucose to H2 in galactose from nuclear Overhauser effect spectroscopy experiments agree with one of the conformations of the trisaccharide in one of the three 100 ps aqueous simulations (ϕ/ψ ca. −100°/150°), indicating this may be a dominant solution conformation. The rms fluctuations of the ϕ‐ and ψ‐dihedral angles were ∼ 10° for a conformational state, both in the vacuum and the aqueous simulations. For the simulations in vacuum, the agreement with experimental NOE data is reasonable when a constant dielectric of 1 is used (major conformers having ϕ/ψ ca. −100°/150° and −140°/100°), whereas the agreement was poor with a constant dielectric of 80. Translational diffusion coefficients calculated from the simulation of the oligosaccharides were 0.12–0.18 × 10 −5 cm 2 /s and from nmr measurements 0.27 × 10 −5 cm 2 /s. © 1994 John Wiley & Sons, Inc.