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Stepwise copper(I) binding to metallothionein: A mixed cooperative and non-cooperative mechanism

Abstract

Copper is a ubiquitous trace metal of vital importance in that it serves as a cofactor in many metalloenzymes. Excess copper becomes harmful if not sequestered appropriately in the cell. As a metal ion chaperone, metallothionein (MT), has been proposed as key player in zinc and copper homeostasis within the cell. The underlying mechanisms by which MT sequesters and transfers copper ions, and subsequently achieves its proposed biological function remain unknown. Using a combination of electrospray ionization mass spectrometry (ESI-MS), circular dichroism (CD) and emission spectroscopy we report the pH-dependent binding properties of Cu(I) to apo-MT1a. The 20 relative Kf-values for the binding of 1-20 Cu(I) to the 20 cysteine MT, were obtained from computational simulation of the experimental mass spectral results. These data identified the pH-dependent formation of three sequential but different clusters as a function of Cu(I) loading. These data provided the first overall sequence for Cu(I) binding in terms of domain specificity and transient binding site structures. Under cooperative binding at pH 7.4, a series of four clusters form: Cu4SCYS-6, followed by Cu6SCYS-9 (β), then a second Cu4SCYS-6 (α), and finally Cu7SCYS-x (α) (x= up to 11). Upon further addition of Cu(I), a mixture of species is formed in a non-cooperative mechanism, saturating the 20 cysteines of MT1a. Using benzoquinone, a cysteine modifier, we were able to confirm that Cu6SCYS-9 formed solely in the N-terminal β-domain, as well as confirming the existence of the presumed Cu4SCYS-6 cluster in the α-domain. Based on the results of ESI-MS and computational simulation we were able to identify speciation in emission and CD spectra by recording ESI-mass, emission and CD spectral data for the same solutions.

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Publication details

The article was accepted on 27 Mar 2017 and first published on 21 Apr 2017


Article type: Paper
DOI: 10.1039/C7MT00041C
Citation: Metallomics, 2017, Accepted Manuscript
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    Stepwise copper(I) binding to metallothionein: A mixed cooperative and non-cooperative mechanism

    J. S. Scheller, G. W. Irvine, D. L. Wong, A. Hartwig and M. Stillman, Metallomics, 2017, Accepted Manuscript , DOI: 10.1039/C7MT00041C

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