Cation–π effects in the complexation of Na + and K + with Phe, Tyr, and Trp in the gas phase

• Published in: Journal of the American Society for Mass Spectrometry 2000-12, Vol.11 (12), p.1037-1046
• Main Authors: Ryzhov, Victor, Dunbar, Robert C., Cerda, Blas, Wesdemiotis, Chrys
• Format: Article
• Language: English
• Subjects: Cations, Monovalent - chemistry; Chemistry; Exact sciences and technology; General and physical chemistry; Kinetics; Mass Spectrometry; Phenylalanine - chemistry; Potassium - chemistry; Sodium - chemistry; Solubility; Solutions; Static Electricity; Tryptophan - chemistry; Tyrosine - chemistry
• ISSN: 1044-0305; 1879-1123
• DOI: 10.1016/S1044-0305(00)00181-1

Na + and K + gas-phase affinities of the three aromatic amino acids Phe, Tyr, and Trp were measured by the kinetic method. Na + binds these amino acids much more strongly than K +, and for both metal ions the binding strength was found to follow the order Phe ≤ Tyr < Trp. Quantum chemical calculations by density functional theory (DFT) gave the same qualitative ordering, but suggested a somewhat larger Phe/Trp increment. These results are in acceptable agreement with predictions based on the binding of Na + and K + to the side chain model molecules benzene, phenol, and indole, and are also in reasonable agreement with the predictions from purely electrostatic calculations of the side-chain binding effects. The binding energies were compared with those to the aliphatic amino acids glycine and alanine. Binding to the aromatic amino acids was found to be stronger both experimentally and computationally, but the DFT calculations indicate substantially larger increments relative to alanine than shown by the experiments. Possible reasons for this difference are discussed. The metal ion binding energies show the same trends as the proton affinities.