Abstract
High-field proton (1H) nuclear magnetic resonance (NMR) spectroscopy has been employed to evaluate the formation of substance P carbamate in aqueous solution. Equilibration of substance P with physiologically relevant concentrations of bicarbonate (2.50 x 10(-2) mol.dm-3) at pH 7.00 generated a new multiplet signal centred at 4.13 ppm in its NMR spectrum, characteristic of the alpha-proton of peptide carbamate species. High-field 1H NMR spectroscopy also demonstrated that the model dipeptide, Arg-Gly, formed a carbamate in neutral aqueous solutions containing 2.50 x 10(-2) mol.dm-3 HCO3-. The physiological significance of these results is discussed in view of the central roles of vasoactive neuropeptides in human joint diseases and the hypercapnic environment of the inflamed rheumatoid joint.
| Original language | English |
|---|---|
| Pages (from-to) | 249-252 |
| Journal | FEBS Letters |
| Volume | 329 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 30 Aug 1993 |
Bibliographical note
Note: This work was supported by the Arthritis and Rheumatism Council (UK).Keywords
- Allied health professions and studies