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PMID: 9407118 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression, purification, and metal binding properties of the N-terminal domain from the wilson disease putative copper-transporting ATPase (ATP7B).

The Journal of biological chemistry ·Vol. 272 ·No. 52 ·1997-12-26 ·Pages 33279-82

DiDonato M, Narindrasorasak S, Forbes JR, Cox DW, Sarkar B

Abstract

The putative copper binding domain from the copper-transporting ATPase implicated in Wilson disease (ATP7B) has been expressed and purified as a fusion to glutathione S-transferase. Immobilized metal ion affinity chromatography revealed that the fusion protein is able to bind to columns charged with different transition metals with varying affinities as follows: Cu(II)>>Zn(II)>Ni(II)>Co(II). The fusion protein did not bind to columns charged with Fe(II) or Fe(III). 65Zinc(II) blotting analysis showed that the domain is able to bind Zn(II) over a range of pH values from 6.5 to 9.0. Competition 65Zn(II) blotting showed that Cd(II), Hg(II), Au(III), and Fe(III) can successfully compete with Zn(II), at comparable concentrations, for binding to the domain. In contrast, the domain had little or no affinity for Ca(II), Mg(II), Mn(II), and Ni(II) relative to copper. Neutron activation analysis of the copper bound to the domain showed a copper:protein ratio of 6.5-7.3:1. Both Cu(II) and Cu(I) were found to have a higher affinity for the domain relative to Zn(II). In addition, a sharp, reproducible transition was only observed in competition experiments with copper, which may suggest that copper binding has some degree of cooperativity.

MeSH Terms
Adenosine Triphosphatases/isolation & purification,metabolism Binding, Competitive Carrier Proteins/isolation & purification,metabolism Cation Transport Proteins Cobalt/metabolism Copper/metabolism Copper-Transporting ATPases Escherichia coli Hepatolenticular Degeneration/enzymology Humans Hydrogen-Ion Concentration In Vitro Techniques Metals, Heavy/metabolism Nickel/metabolism Zinc/metabolism
Chemicals
Carrier Proteins Cation Transport Proteins Metals, Heavy Cobalt Copper Nickel Adenosine Triphosphatases ATP7B protein, human Copper-Transporting ATPases Zinc
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
DiDonato M
Department of Biochemistry Research, The Hospital for Sick Children, Toronto, Ontario, M5G 1X8 Canada.
Narindrasorasak S
Forbes J R
Cox D W
Sarkar B
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1997-12-26
Pages
33279-82
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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