Function and regulation of the mammalian copper-transporting ATPases: Insights from biochemical and cell biological approaches

被引:161
作者
Lutsenko, S
Petris, NJ
机构
[1] Oregon Hlth Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA
[2] Univ Missouri, Dept Nutrit Sci, Columbia, MO 65211 USA
关键词
copper; Menkes disease; Wilson's disease; ATP7A; ATP7B; transport; trafficking; regulation;
D O I
10.1007/s00232-002-1040-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Copper is an essential trace element that plays a very important role in cell physiology. In humans, disruption of normal copper homeostasis leads to severe disorders, such as Menkes disease and Wilson's disease. Recent genetic, cell biological, and biochemical studies have begun to dissect the molecular mechanisms involved in transmembrane transport and intracellular distribution of copper in mammalian cells. In this review, we summarize the advances that have been made in understanding of structure, function, and regulation of the key human copper transporters, the Menkes disease and Wilson's disease proteins.
引用
收藏
页码:1 / 12
页数:12
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