Combined use of Overhauser spectroscopy and NMR diffusion experiments for mapping the hydration structure of nucleosides : structure and dynamics of uridine in water

Copyright 2006 John Wiley & Sons, Ltd.

Détails bibliographiques
Publié dans:Magnetic resonance in chemistry : MRC. - 1985. - 44(2006), 12 vom: 20. Dez., Seite 1109-17
Auteur principal: Seba, Hadj B (Auteur)
Autres auteurs: Thureau, Pierre, Ancian, Bernard, Thévand, André
Format: Article
Langue:English
Publié: 2006
Accès à la collection:Magnetic resonance in chemistry : MRC
Sujets:Journal Article Nucleosides Water 059QF0KO0R Uridine WHI7HQ7H85
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520 |a Complementary results from 13C intermolecular nuclear Overhauser effects (NOE), 1H-13C heteronuclear Overhauser spectroscopy (HOSEY) and 1H-NMR diffusion measurements were used for probing the structure of the first solvation shell of uridine in water. It is demonstrated that a cyclic dihydrate is formed. The two water molecules produce two hydrogen bonds with the two oxygen atoms from the pyrimidine ring and accept only one hydrogen bond from the amide proton. The dihydrate has only a short lifetime as compared with the rotational correlation time of the free nucleoside. The chemical exchange constant of the amide proton with water is then estimated by diffusion experiments. The results are consistent with previous data obtained for uracil in water and provide interesting information about water accessibility in nucleic acid bases 
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