Theoretical calculations of stability constants and pKa values of metal complexes in solution: application to pyridoxamine-copper(II) complexes and their biological implications in AGE inhibition

Abstract

[eng] Accurate prediction of thermodynamic constants of chemical reactions in solution is one of the current challenges in computational chemistry. We report a scheme for predicting stability constants (log β) and pKa values of metal complexes in solution by means of calculating free energies of ligand- and proton-exchange reactions using Density Functional Theory calculations in combination with a continuum solvent model. The accuracy of the predicted log β and pKa values (mean absolute deviations of 1.4 and 0.2 units respectively) is equivalent to the experimental uncertainties. This theoretical methodology provides direct knowledge of log β and pKa values of major and minor species, so it is of potential use in combination with experimental techniques to obtain a detailed description of the microscopic equilibria. In particular, the proposed methodology is shown to be especially useful for obtaining the real acidity constants of those chelates where the metal<br>ligand coordination changes as a result of ligand deprotonation. The stability and acidity constants of pyridoxamine<br>Cu2+ chelates calculated with the proposed methodology show that pyridoxamine is an efficient scavenging agent of Cu2+ under physiological pH conditions. This is of special interest as Cu2+ overload is involved in the formation of advanced glycation end-products (AGEs) and their associated degenerative medical conditions.