Gly-His-Thr-Asp-Amide, an Insulin-Activating Peptide from the Human Pancreas Is a Strong Cu(II) but a Weak Zn(II) Chelator

Radosław Kotuniak; Tomasz Frączyk; Piotr Skrobecki; Dawid Płonka; Wojciech Bal

doi:10.1021/acs.inorgchem.8b02841

Gly-His-Thr-Asp-Amide, an Insulin-Activating Peptide from the Human Pancreas Is a Strong Cu(II) but a Weak Zn(II) Chelator

Inorg Chem. 2018 Dec 17;57(24):15507-15516. doi: 10.1021/acs.inorgchem.8b02841. Epub 2018 Nov 27.

Authors

Radosław Kotuniak¹, Tomasz Frączyk^{1

2}, Piotr Skrobecki¹, Dawid Płonka¹, Wojciech Bal¹

Affiliations

¹ Institute of Biochemistry and Biophysics , Polish Academy of Sciences , Pawińskiego 5a , 02-106 Warsaw , Poland.
² Department of Immunology, Transplantology and Internal Medicine , Medical University of Warsaw , Nowogrodzka 59 , 02-006 Warsaw , Poland.

PMID: 30480433
DOI: 10.1021/acs.inorgchem.8b02841

Abstract

The Cu(II) and Zn(II) binding abilities of Gly-His-Thr-Asp-amide (GHTD-am), a tetrapeptide coreleased from the pancreas along with insulin, were studied using UV-vis and circular dichroism spectroscopies, potentiometry, and calorimetry. GHTD-am is a very strong Cu(II) chelator, forming a three-nitrogen complex with a conditional affinity constant ^C K at pH 7.4 of 4.5 × 10¹² M^-1. The fourth coordination site can be occupied by a solvent molecule or a ternary ligand, such as imidazole, with ^C K on the order of several hundred reciprocal molar. The Zn(II) binding ability of GHTD-am is relatively weak, with ^C K values at pH 7.4 of 3.0 × 10⁴ and 2.0 × 10³ M^-1 for the first and second GHTD-am molecule coordinated, respectively. These results are discussed in light of the modes of interactions of Zn(II) and Cu(II) ions with insulin. A direct effect of GHTD-am on the Zn(II) interactions with insulin is unlikely, but its Cu(II) complex may have a biological relevance because of its high affinity and ability to form ternary complexes.