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Updated: Jun 4, 2026

Mass Spectrometric Approaches to Study Protein Structure and Interactions in Lyophilized Powders
Published on: April 14, 2015
Spectroscopy study on the noncovalent interactions in the binary and ternary systems of L-lysine, adenosine
1State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, Gansu, China.
Abstract:
Intermolecular interactions of adenosine 5'-triphosphate (ATP) with Lysine (Lys) and Mg(2+) were studied in aqueous solution by (1)H and (31)P NMR spectra. In the metal-free system, the N-1 atom of the purine ring of ATP and carboxyl group of Lys are the interaction sites at low pH conditions. With increasing pH, the interaction efficiency between the phosphate group of ATP and the protonated ammonium group of Lys increased significantly, while that with carboxyl group in Lys decreased. In the Mg(2+)-Lys-ATP system, multi-interactions, such as coordination, cations (Mg(2+), NH(3)(+))-π, hydrogen bonding, ion-pairing interactions and electrostatic interactions co-existed. In addition, the recognition of ATP by the amino acid cation (Lys) was significantly promoted by the addition of magnesium ion, which led to the coordination competition between Lys and ATP.
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