Inhibition of calcium-calmodulin complex formation by vasorelaxant basic dipeptides demonstrated by in vitro and in silico analyses

Background Tryptophan-histidine (Trp-His) was found to suppress the activity of the Ca^{2 +}/calmodulin (CaM)-dependent protein kinases II (CaMKII), which requires the Ca^{2 +}-CaM complex for an initial activation. In this study, we attempted to clarify whether Trp-His inhibits Ca^{2 +}-CaM complex formation, a CaMKII activator. Methods The ability of Trp-His and other peptides to inhibit Ca^{2 +}-CaM complex formation was investigated by a Ca^{2 +}-encapsulation fluorescence assay. The peptide-CaM interactions were illustrated by molecular dynamic simulation. Results We showed that Trp-His inhibited Ca^{2 +}-CaM complex formation with a 1:1 binding stoichiometry of the peptide to CaM, considering that Trp-His reduced Hill coefficient of Ca^{2 +}-CaM binding from 2.81 to 1.92. His-Trp also showed inhibitory activity, whereas Trp + His, 3-methyl His-Trp, and Phe-His did not show significant inhibitory activity, suggesting that the inhibitory activity was due to a peptide skeleton (irrespective of the sequence), a basic amino acid, a His residue, the N hydrogen atom of its imidazole ring, and Trp residue. In silico studies suggested the possibility that Trp-His and His-Trp interacted with the Ca^{2 +}-binding site of CaM by forming hydrogen bonds with key Ca^{2 +}-binding residues of CaM, with a binding free energy of - 49.1 and - 68.0 kJ/mol, respectively. Conclusions This is the first study demonstrating that the vasoactive dipeptide Trp-His possesses inhibitory activity against Ca^{2 +}-CaM complex formation, which may elucidate how Trp-His inhibited CaMKII in a previous study. General significance The results provide a basic idea that could lead to the development of small peptides binding with high affinity to CaM and inhibiting Ca^{2 +}-CaM complex formation in the future.