Biochimica et Biophysica Acta 2014-10-01

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

Thanutchaporn Kumrungsee, Tomomi Saiki, Sayaka Akiyama, Kentaro Nakashima, Mitsuru Tanaka, Yutaro Kobayashi, Toshiro Matsui

Index: Biochim. Biophys. Acta 1840(10) , 3073-8, (2014)

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Abstract

Tryptophan-histidine (Trp-His) was found to suppress the activity of the Ca²⁺/calmodulin (CaM)-dependent protein kinases II (CaMKII), which requires the Ca²⁺-CaM complex for an initial activation. In this study, we attempted to clarify whether Trp-His inhibits Ca²⁺-CaM complex formation, a CaMKII activator.The ability of Trp-His and other peptides to inhibit Ca²⁺-CaM complex formation was investigated by a Ca²⁺-encapsulation fluorescence assay. The peptide-CaM interactions were illustrated by molecular dynamic simulation.We showed that Trp-His inhibited Ca²⁺-CaM complex formation with a 1:1 binding stoichiometry of the peptide to CaM, considering that Trp-His reduced Hill coefficient of Ca²⁺-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 Ca²⁺-binding site of CaM by forming hydrogen bonds with key Ca²⁺-binding residues of CaM, with a binding free energy of -49.1 and -68.0 kJ/mol, respectively.This is the first study demonstrating that the vasoactive dipeptide Trp-His possesses inhibitory activity against Ca²⁺-CaM complex formation, which may elucidate how Trp-His inhibited CaMKII in a previous study.The results provide a basic idea that could lead to the development of small peptides binding with high affinity to CaM and inhibiting Ca²⁺-CaM complex formation in the future.Copyright © 2014 Elsevier B.V. All rights reserved.