Journal article
Role of glutaredoxin1 and glutathione in regulating the activity of the copper-transporting P-type ATPases, ATP7A and ATP7B
WCJ Singleton, KT McInnes, MA Cater, WR Winnall, R McKirdy, Y Yu, PE Taylor, BX Ke, DR Richardson, JFB Mercer, S La Fontaine
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2010
Abstract
The copper-transporting P-type ATPases (Cu-ATPases), ATP7A and ATP7B, are essential for the regulation of intracellular copper homeostasis. In this report we describe new roles for glutathione (GSH) and glutaredoxin1 (GRX1) in Cu homeostasis through their regulation of Cu-ATPase activity. GRX1 is a thiol oxidoreductase that catalyzes the reversible reduction of GSH-mixed disulfides to their respective sulfhydryls (deglutathionylation). Here, we demonstrated that glutathionylation of the Cu-ATPases and their interaction with GRX1 were affected by alterations in Cu levels. The data support our hypothesis that the Cu-ATPases serve as substrates for Cu-dependent GRX1-mediated deglutathionylation..
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Funding Acknowledgements
This work was supported by grants from Deakin University and the National Health and Medical Research Council of Australia (NHMRC) (to S. L. and J. F. B. M.), a NHMRC biomedical research fellowship (to M. A. C.), a NHMRC senior principal research fellowship and grants from the NHMRC and the Australian Research Council (to D. R. R.), and a University of Sydney Faculty of Medicine postgraduate scholarship and Cancer Institute of New South Wales research scholarship (to Y. Y.).