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铜伴侣蛋白Atox1对基于硫醇的铜的处理

Thiol-based copper handling by the copper chaperone Atox1.

作者信息

Hatori Yuta, Inouye Sachiye, Akagi Reiko

机构信息

Department of Pharmacy, Yasuda Women's University, Yasuhigashi, Asaminami-ku, Hiroshima, Japan.

出版信息

IUBMB Life. 2017 Apr;69(4):246-254. doi: 10.1002/iub.1620. Epub 2017 Mar 15.

Abstract

Human antioxidant protein 1 (Atox1) plays a crucial role in cellular copper homeostasis. Atox1 captures cytosolic copper for subsequent transfer to copper pumps in trans Golgi network, thereby facilitating copper supply to various copper-dependent oxidereductases matured within the secretory vesicles. Atox1 and other copper chaperones handle cytosolic copper using Cys thiols which are ideal ligands for coordinating Cu(I). Recent studies demonstrated reversible oxidation of these Cys residues in copper chaperones, linking cellular redox state to copper homeostasis. Highlighted in this review are unique redox properties of Atox1 and other copper chaperones. Also, summarized are the redox nodes in the cytosol which potentially play dominant roles in the redox regulation of copper chaperones. © 2016 IUBMB Life, 69(4):246-254, 2017.

摘要

人类抗氧化蛋白1(Atox1)在细胞铜稳态中起着关键作用。Atox1捕获胞质铜,随后将其转移至反式高尔基体网络中的铜泵,从而促进铜供应给在分泌小泡内成熟的各种铜依赖性氧化还原酶。Atox1和其他铜伴侣蛋白利用半胱氨酸硫醇来处理胞质铜,半胱氨酸硫醇是配位Cu(I)的理想配体。最近的研究表明,铜伴侣蛋白中这些半胱氨酸残基会发生可逆氧化,将细胞氧化还原状态与铜稳态联系起来。本综述重点介绍了Atox1和其他铜伴侣蛋白独特的氧化还原特性。此外,还总结了胞质中可能在铜伴侣蛋白氧化还原调节中起主导作用的氧化还原节点。©2016国际生物化学与分子生物学联盟生命科学部,69(4):246 - 254,2017。

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