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Metal binding selectivity of an N-terminally free multihistidine peptide HAVAHHH-NH2

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Abstract

Copper(II), nickel(II), zinc(II) and organometallic ruthenium(II) ([(η6-p-cym)Ru(H2O)3]2+) complexes of an N-terminally free heptapeptide containing four histidyl residues (NH2-HAVAHHH-NH2) have been studied by potentiometric and various spectroscopic techniques (UV-vis, CD, NMR and ESI-MS). The data revealed a significant selectivity in the metal binding ability of this ligand. Histamine-like coordination of the amino terminus is the primary binding mode for all metal ions but the internal histidyl residues can also contribute to the overall stability of the complexes. Copper(II) and nickel(II) ions are able to induce the deprotonation and coordination of the amide functions both at the amino terminus and around the internal histidyl sites, resulting in the co-existence of various coordination isomers or the formation of dinuclear complexes in the presence of excess of metal ions.

Graphical abstract: Metal binding selectivity of an N-terminally free multihistidine peptide HAVAHHH-NH2

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Publication details

The article was received on 06 Sep 2018, accepted on 03 Dec 2018 and first published on 05 Dec 2018


Article type: Paper
DOI: 10.1039/C8NJ04538K
Citation: New J. Chem., 2019, Advance Article
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    Metal binding selectivity of an N-terminally free multihistidine peptide HAVAHHH-NH2

    B. D. Balogh, Z. Bihari, P. Buglyó, G. Csire, Z. Kerekes, M. Lukács, I. Sóvágó and K. Várnagy, New J. Chem., 2019, Advance Article , DOI: 10.1039/C8NJ04538K

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