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哺乳动物铜转运ATP酶的功能与调控:来自生物化学和细胞生物学方法的见解

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

作者信息

Lutsenko S, Petris M J

机构信息

Department of Biochemistry and Molecular Biology, Oregon Health & Science University, 3181 Sam Jackson Park Rd, Portland, OR 97201, USA.

出版信息

J Membr Biol. 2003 Jan 1;191(1):1-12. doi: 10.1007/s00232-002-1040-6.

Abstract

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.

摘要

铜是一种必需的微量元素,在细胞生理过程中发挥着非常重要的作用。在人类中,正常铜稳态的破坏会导致严重疾病,如门克斯病和威尔逊病。最近的遗传学、细胞生物学和生物化学研究已开始剖析哺乳动物细胞中铜的跨膜运输和细胞内分布所涉及的分子机制。在本综述中,我们总结了在理解关键人类铜转运蛋白、门克斯病蛋白和威尔逊病蛋白的结构、功能及调节方面所取得的进展。

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