N.m.r. analyses of the histidine microenvironments in a human salivary proline‐rich glycoprotein
- 1 August 1988
- journal article
- research article
- Published by Wiley in International Journal of Peptide and Protein Research
- Vol. 32 (2) , 123-129
- https://doi.org/10.1111/j.1399-3011.1988.tb00672.x
Abstract
The pKa's of the three histidine residues in a proline‐rich glycoprotein from human parotid saliva (PRG) were determined by 360 MHz proton n.m.r. spectroscopy. The addition of calcium (0.64 mm) caused drops in the pKa's of all three histidines by ∼0.25 units. When imidazole and cyclo(l‐histidine‐l‐proline) were used as model compounds, corresponding concentrations of calcium had no effect on their pKa's. Also, the model compounds gave absolute pKa values in good agreement with similar chemical species reported in the literature. Exchange lifetime data and previously reported hydrogen → deuterium exchange experiments suggest that the PRG histidine NtH protons are not involved in hydrogen‐bonds. Collectively, these data imply that changes in PRG conformation occur upon the addition of calcium.Keywords
This publication has 17 references indexed in Scilit:
- N.m.r. and computer‐simulated conformational analyses of a nonapeptide found in a human salivary proline‐rich glycoproteinInternational Journal of Peptide and Protein Research, 1988
- Structural Aspects of Salivary GlycoproteinsJournal of Dental Research, 1987
- Circular dichroism and fluorescence spectroscopic analyses of a proline‐rich glycoprotein from human parotid salivaInternational Journal of Peptide and Protein Research, 1985
- Structure of the carbohydrate chains of the proline-rich glycoprotein from human parotid salivaBiochemical and Biophysical Research Communications, 1982
- NMR STUDY ON THE PROTONATION OF IMIDAZOLE RING OF N-ACETYL-l-HISTIDINE METHYLAMIDE, A MODEL FOR HISTIDINE RESIDUES EXPOSED TO AQUEOUS SOLVENTChemistry Letters, 1978
- Quantitative Study of the Interaction of Salivary Acidic Proline-Rich Proteins with HydroxyapatiteCaries Research, 1978
- Evidence from circular dichroism for the binding of hydrogen ions and calcium ions by poly(L‐proline)Biopolymers, 1976
- Observation of histidine residues in proteins by nuclear magnetic resonance spectroscopyAccounts of Chemical Research, 1975
- A Nuclear Magnetic Resonance Study of Poly(L-proline) in Aqueous and Aqueous Salt SolutionsMacromolecules, 1971
- Circular dichroism of poly‐L‐proline in an unordered conformationBiopolymers, 1968