Title of article
Trace elements in human physiology and pathology. Copper
Author/Authors
H. Tapiero، نويسنده , , D. M. Townsend، نويسنده , , K. D. Tew، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
13
From page
386
To page
398
Abstract
Copper is a trace element, important for the function of many cellular enzymes. Copper ions can adopt distinct redox states oxidized Cu(II) or reduced (I), allowing the metal to play a pivotal role in cell physiology as a catalytic cofactor in the redox chemistry of enzymes, mitochondrial respiration, iron absorption, free radical scavenging and elastin cross-linking. If present in excess, free copper ions can cause damage to cellular components and a delicate balance between the uptake and efflux of copper ions determines the amount of cellular copper. In biological systems, copper homeostasis has been characterized at the molecular level. It is coordinated by several proteins such as glutathione, metallothionein, Cu-transporting P-type ATPases, Menkes and Wilson proteins and by cytoplasmic transport proteins called copper chaperones to ensure that it is delivered to specific subcellular compartments and thereby to copper-requiring proteins.
Keywords
Copper , enzymes , bioavailability , Ceruloplasmin , Metallothionein , deficiency
Journal title
Biomedicine and Pharmacotherapy
Serial Year
2003
Journal title
Biomedicine and Pharmacotherapy
Record number
477533
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