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本文引用的文献

1
Mfc1 is a novel forespore membrane copper transporter in meiotic and sporulating cells.Mfc1 是减数分裂和孢子形成细胞中新的前孢子膜铜转运蛋白。
J Biol Chem. 2011 Sep 30;286(39):34356-72. doi: 10.1074/jbc.M111.280396. Epub 2011 Aug 2.
2
Cisplatin binds human copper chaperone Atox1 and promotes unfolding in vitro.顺铂与人铜伴侣蛋白 Atox1 结合并促进体外展开。
Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):6951-6. doi: 10.1073/pnas.1012899108. Epub 2011 Apr 11.
3
Model peptides provide new insights into the role of histidine residues as potential ligands in human cellular copper acquisition via Ctr1.模型肽为组氨酸残基作为潜在配体通过 Ctr1 参与人体细胞铜摄取提供了新的见解。
J Am Chem Soc. 2011 Mar 30;133(12):4427-37. doi: 10.1021/ja108890c. Epub 2011 Mar 4.
4
The intracellular Arabidopsis COPT5 transport protein is required for photosynthetic electron transport under severe copper deficiency.拟南芥细胞内的 COPT5 转运蛋白在严重铜缺乏下对光合作用电子传递是必需的。
Plant J. 2011 Mar;65(6):848-60. doi: 10.1111/j.1365-313X.2010.04472.x. Epub 2011 Feb 1.
5
Dissection of the relative contribution of the Schizosaccharomyces pombe Ctr4 and Ctr5 proteins to the copper transport and cell surface delivery functions.解析裂殖酵母 Ctr4 和 Ctr5 蛋白对铜转运和细胞表面递呈功能的相对贡献。
Microbiology (Reading). 2011 Apr;157(Pt 4):1021-1031. doi: 10.1099/mic.0.046854-0. Epub 2011 Jan 27.
6
Acquisition of dietary copper: a role for anion transporters in intestinal apical copper uptake.膳食铜的摄取:阴离子转运体在肠道顶端铜摄取中的作用。
Am J Physiol Cell Physiol. 2011 Mar;300(3):C588-99. doi: 10.1152/ajpcell.00054.2010. Epub 2010 Dec 29.
7
Coordination of platinum therapeutic agents to met-rich motifs of human copper transport protein1.协调铂类治疗剂与人铜转运蛋白 1 的富金属基序。
Metallomics. 2010 Jan;2(1):74-83. doi: 10.1039/b916899k. Epub 2009 Nov 2.
8
Ctr1 is an apical copper transporter in mammalian intestinal epithelial cells in vivo that is controlled at the level of protein stability.Ctr1 是体内哺乳动物肠道上皮细胞中的顶端铜转运蛋白,其蛋白稳定性受到调控。
J Biol Chem. 2010 Oct 15;285(42):32385-92. doi: 10.1074/jbc.M110.143826. Epub 2010 Aug 10.
9
Altered microglial copper homeostasis in a mouse model of Alzheimer's disease.阿尔茨海默病小鼠模型中,小胶质细胞铜稳态的改变。
J Neurochem. 2010 Sep;114(6):1630-8. doi: 10.1111/j.1471-4159.2010.06888.x. Epub 2010 Aug 19.
10
C(alpha)-trace model of the transmembrane domain of human copper transporter 1, motion and functional implications.人铜转运蛋白 1 的跨膜域的 C(alpha)-trace 模型,运动与功能的意义。
Proc Natl Acad Sci U S A. 2010 Jun 15;107(24):10908-13. doi: 10.1073/pnas.0914717107. Epub 2010 Jun 1.

SLC31(CTR)家族铜转运体在健康和疾病中的作用。

SLC31 (CTR) family of copper transporters in health and disease.

机构信息

University of Nebraska-Lincoln, Dept. of Biochemistry and Redox Biology Center, Lincoln, NE 68588, USA.

出版信息

Mol Aspects Med. 2013 Apr-Jun;34(2-3):561-70. doi: 10.1016/j.mam.2012.07.011.

DOI:10.1016/j.mam.2012.07.011
PMID:23506889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3602788/
Abstract

Copper is a vital mineral for many organisms, yet it is highly toxic as demonstrated by serious health concerns associated with its deficiency or excess accumulation. The SLC31 (CTR) family of copper transporters is a major gateway of copper acquisition in eukaryotes, ranging from yeast to humans. Characterization of the function, modes of action, and regulation of CTR and other molecular factors that functionally cooperate with CTR for copper transport, compartmentalization, incorporation into cuproproteins, and detoxification has revealed that organisms have evolved fascinating mechanisms for tight control of copper metabolism. This research progress further indicates the significance of copper in health and disease and opens avenues for therapeutic control of copper bioavailability and its metabolic pathways.

摘要

铜是许多生物体必需的矿物质,但它也具有高度毒性,其缺乏或过量积累会导致严重的健康问题。SLC31(CTR)家族的铜转运蛋白是真核生物(从酵母到人类)获取铜的主要途径。对 CTR 及其与铜转运、区室化、掺入铜蛋白和解毒功能上合作的其他分子因子的功能、作用模式和调控的研究,揭示了生物体进化出了令人着迷的机制来严格控制铜代谢。这一研究进展进一步表明了铜在健康和疾病中的重要性,并为铜生物利用度及其代谢途径的治疗性控制开辟了道路。