The splitting pattern of the P-H5" (and P-H5') cross-peak in a 2D 31P-1H correlated NMR spectrum is analysed. Since this cross-peak pattern is strongly dependent on two coupling constants, 'J(PH5") and 3J(H4H5"), it is an efficient probe for the backbone torsion angles fl and y in nucleic acids. A m
Kinetics of 1H → 31P NMR cross-polarization in bone apatite and its mineral standards
✍ Scribed by Agnieszka Kaflak; Waclaw Kolodziejski
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 176 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2207
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✦ Synopsis
Abstract
Kinetics of NMR cross‐polarization (CP) from protons to phosphorus‐31 nuclei was studied in the following samples: mineral of whole human bone, apatite prepared from bone, natural brushite, synthetic hydroxyapatite (hydrated and calcined), and synthetic carbonatoapatite of type B with 9 wt% of CO~3~^2−^. In order to avoid an effect of magic angle spinning on CP and relaxation, the experiments were carried out on static samples. Parameters of the CP kinetics were discussed for trabecular and cortical bone tissue from adult subjects in comparison to the synthetic mineral standards. It was found that carbonatoapatite shows similar CP behavior to the bone mineral. Both materials undergo two‐component CP kinetics. The fast‐relaxing classical component is from the surface of apatite crystals and the slow‐relaxing nonclassical component comes from the crystal interior. The components have been unambiguously assigned using inverse CP from phosphorus‐31 to protons. The study provides information on a structured water layer, which covers crystal surface of carbonato‐ and bone apatite. The layer encompasses ca 40% of apatite phosphorus and its thickness is more than ca 2 nm. Copyright © 2008 John Wiley & Sons, Ltd.
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