Advances in the understanding of mammalian copper transporters.
Adv Nutr. 2011 Mar; 2(2):129-37.AN

Abstract

Copper (Cu) is an essential micronutrient. Its ability to exist in 2 oxidation states (Cu(1+) and Cu(2+)) allows it to function as an enzymatic cofactor in hydrolytic, electron transfer, and oxygen utilization reactions. Cu transporters CTR1, ATP7A, and ATP7B play key roles in ensuring that adequate Cu is available for Cu-requiring processes and the prevention of excess Cu accumulation within cells. Two diseases of Cu metabolism, Menkes disease and Wilson disease, which are caused by mutations in ATP7A and ATP7B, respectively, exemplify the critical importance of regulating Cu balance in humans. Herein, we review recent studies of the biochemical and cell biological characteristics of CTR1, ATP7A, and ATP7B, as well as emerging roles for Cu in new areas of physiology.

Links

Publisher Full Text
ncbi.nlm.nih.gov
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Authors+Show Affiliations

Wang Y
Department of Biochemistry, University of Missouri, Columbia, MO 65211, USA.
Hodgkinson V
No affiliation info available
Zhu S
No affiliation info available
Weisman GA
No affiliation info available
Petris MJ
No affiliation info available

MeSH

Adenosine TriphosphatasesAnimalsBiological TransportCation Transport ProteinsCopperCopper Transporter 1Copper-Transporting ATPasesEpithelial CellsHepatolenticular DegenerationHumansMammalsMenkes Kinky Hair SyndromeSLC31 ProteinsTrace Elements

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Review

Language

eng

PubMed ID

22332042