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新生正常小鼠和斑驳突变小鼠肝脏及肾脏组织中铜结合蛋白的研究。

A study of the copper-binding proteins in liver and kidney tissue of neonatal normal and mottled mutant mice.

作者信息

Port A E, Hunt D M

出版信息

Biochem J. 1979 Dec 1;183(3):721-30. doi: 10.1042/bj1830721.

DOI:10.1042/bj1830721
PMID:575486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1161654/
Abstract

The Cu2+-binding proteins from liver and kidney tissue of 7--8-day-old brindled (Mobr) mice and their normal littermates were compared. (1) Separation over Bio-Gel P-10 showed that the differences in the Cu2+ content of mutant tissues were largely associated with a low-molecular-weight protein fraction (mol.wt. 14 500). (2) Further purification of this low-molecular-weight fraction by anion-exchange chromatography revealed four subfractions. The Cu2+ content of each subfraction reflected the Cu2+ status of the tissue of origin; the Cu2+ contents of the mutant kidney subfractions were elevated and those of the mutant liver were depressed compared with normal. In contrast, the protein contents of the subfractions were less variable and did not reflect the differing Cu2+ contents. (3) Amino acid analysis of the four subfractions from CuCl2-treated mutant and normal animals revealed clos similarities. The proteins showed high glycine, glutamic acid, serine, alanine and lysine contents and a rather variable cysteine content. Differences were apparent in the normal liver subfractions, which showed a higher cysteine content and lower glutamic acid content than did either the mutant liver or normal and mutant kidney subfractions. These observations, together with the recorded presence of aromatic amino acids, indicated that these proteins are not thioneins.

摘要

对7 - 8日龄花斑(Mobr)小鼠及其正常同窝仔鼠肝脏和肾脏组织中的铜离子结合蛋白进行了比较。(1)在Bio - Gel P - 10上的分离表明,突变组织中铜离子含量的差异主要与低分子量蛋白组分(分子量14500)有关。(2)通过阴离子交换色谱对该低分子量组分进一步纯化后得到四个亚组分。每个亚组分的铜离子含量反映了其来源组织的铜离子状态;与正常情况相比,突变型肾脏亚组分的铜离子含量升高,而突变型肝脏的铜离子含量降低。相比之下,亚组分的蛋白质含量变化较小,且不能反映不同的铜离子含量。(3)对来自氯化铜处理的突变型和正常动物的四个亚组分进行氨基酸分析,结果显示它们非常相似。这些蛋白质的甘氨酸、谷氨酸、丝氨酸、丙氨酸和赖氨酸含量较高,半胱氨酸含量变化较大。正常肝脏亚组分存在明显差异,其半胱氨酸含量高于突变型肝脏以及正常和突变型肾脏亚组分,而谷氨酸含量则低于这些亚组分。这些观察结果,连同所记录的芳香族氨基酸的存在,表明这些蛋白质不是硫蛋白。

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引用本文的文献

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2
The effect of copper supplementation on the concentration of copper in the brain of the brindled mouse.补充铜对花斑小鼠大脑中铜浓度的影响。
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Hepatic metallothionein synthesis in neonatal Mottled-Brindled mutant mice.新生斑驳-条纹突变小鼠肝脏金属硫蛋白的合成
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Copper in brain.大脑中的铜
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Neuropathologic study in the heterozygotes of X-linked brindled mutant mouse.X连锁斑驳突变小鼠杂合子的神经病理学研究
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本文引用的文献

1
A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration.一种伴性隐性疾病,伴有生长发育迟缓、特殊毛发以及局灶性脑和小脑变性。
Pediatrics. 1962 May;29:764-79.
2
DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS.圆盘电泳。II. 方法及其在人血清蛋白中的应用。
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Metallothionein: a cadmium- and zinc-containing protein from equine renal cortex.金属硫蛋白:一种来自马肾皮质的含镉和锌的蛋白质。
J Biol Chem. 1960 Dec;235:3460-5.
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Tissue sulfhydryl groups.组织巯基
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The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis.通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定分子量的可靠性。
J Biol Chem. 1969 Aug 25;244(16):4406-12.
6
Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects.门克斯卷发综合征。一种遗传性铜吸收缺陷病,具有广泛影响。
Pediatrics. 1972 Aug;50(2):188-201.
7
Primary defect in copper transport underlies mottled mutants in the mouse.铜转运的原发性缺陷是小鼠斑驳突变体的基础。
Nature. 1974 Jun 28;249(460):852-4. doi: 10.1038/249852a0.
8
Fluorometric assay of proteins in the nanogram range.纳克级蛋白质的荧光测定法。
Arch Biochem Biophys. 1973 Mar;155(1):213-20. doi: 10.1016/s0003-9861(73)80023-2.
9
An improved procedure for protein staining in polyacrylamide gels with a new type of Coomassie Brilliant Blue.一种使用新型考马斯亮蓝对聚丙烯酰胺凝胶中的蛋白质进行染色的改进方法。
Anal Biochem. 1972 Aug;48(2):617-20. doi: 10.1016/0003-2697(72)90117-0.
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Small copper-binding proteins from normal and copper-loaded liver.来自正常肝脏和铜负荷肝脏的小铜结合蛋白。
Biochim Biophys Acta. 1975 Dec 5;411(2):393-8. doi: 10.1016/0304-4165(75)90322-0.