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Cation-Binding of Glutamate in Aqueous Solution.

Sergej FriesenSergey E KruchininMarina V FedotovaRichard Buchner
Published in: The journal of physical chemistry. B (2024)
Interactions of the cations Li + , Na + , Mg 2+ , and Ca 2+ with L-glutamate (Glu - ) in aqueous solution were studied at room temperature with dielectric relaxation spectroscopy in the gigahertz region. Spectra of ∼0.4 M NaGlu with added LiCl, NaCl, MgCl 2 , or CaCl 2 ( c (MCl n ) ≤ 1.5 M) were evaluated and experiments supplemented by density functional theory and 3D reference interaction site model (3D-RISM) calculations. In addition to the modes found for aqueous NaGlu, namely, the reorientation of free Glu - ions (peaking at ∼1.6 GHz), of moderately retarded H 2 O molecules hydrating the carboxylate moieties of Glu - (∼8.4 GHz), of the cooperative resettling of the H-bond network of bulk water (∼20 GHz), and its preceding fast H-bond flip (∼400 GHz), an additional low-frequency relaxation at ∼0.4 GHz was detected upon the addition of the four salts. In the case of NaGlu + MgCl 2 (aq) and NaGlu + CaCl 2 (aq), this mode could be unequivocally assigned to an ion pair formed by the cation and the side-chain carboxylate moiety of Glu - . For NaGlu + LiCl(aq), either this species or a backbone-[Li + -H 2 O-Cl - -Glu - ] triple ion is formed. Binding constants increase in the order Li + <Mg 2+ <Ca 2+ . For NaGlu + NaCl(aq), an assignment of the ∼0.4 GHz mode to ion pairs or triples was not plausible. Accordingly, its origin remains speculative here.
Keyphrases
  • aqueous solution
  • density functional theory
  • ionic liquid
  • room temperature
  • molecular dynamics
  • solid state
  • single molecule
  • ion batteries
  • high resolution
  • mass spectrometry
  • dna binding
  • protein kinase
  • genetic diversity