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培养的人皮肤成纤维细胞中金属硫蛋白样蛋白的合成:与门克斯病中铜分布异常的关系。

Synthesis of a metallothionein-like protein in cultured human skin fibroblasts: relation to abnormal copper distribution in Menkes' disease.

作者信息

Bonewitz R F, Howell R R

出版信息

J Cell Physiol. 1981 Mar;106(3):339-48. doi: 10.1002/jcp.1041060303.

Abstract

A metallothionein-like protein (MTP) is synthesized in normal diploid human skin fibroblasts cultured in Zn- or Cu-supplemented medium. Synthesis of MTP is not detected in cells cultured without metal supplementation of complete tissue-culture medium. Cultured fibroblasts from patients with Menkes' disease accumulate excess Cu which chromatographs both with high-molecular-weight protein(s) and with a Cu-MTP. Under normal culture conditions, the Menkes' MTP incorporates [35S]-cystine, but not appreciable amounts of 65Zn. However, Menkes fibroblasts retain the ability to incorporate 65Zn into MTP in response to Zn supplementation of the medium. The results do not support the idea that Menkes' disease results from a failure of Cu to bind to MTP, but rather that an elevated intracellular Cu concentration in Menkes' disease fibroblasts leads to association of excess Cu with high-molecular-weight protein, stimulating synthesis of a Cu-binding MTP.

摘要

一种类金属硫蛋白(MTP)在添加了锌或铜的培养基中培养的正常二倍体人皮肤成纤维细胞中合成。在未添加金属的完全组织培养基中培养的细胞中未检测到MTP的合成。门克斯病患者的培养成纤维细胞会积累过量的铜,这些铜与高分子量蛋白质以及铜 - MTP一起进行色谱分析。在正常培养条件下,门克斯病的MTP会掺入[35S] - 胱氨酸,但不会掺入可观量的65Zn。然而,门克斯病成纤维细胞保留了在培养基中添加锌后将65Zn掺入MTP的能力。这些结果不支持门克斯病是由于铜无法与MTP结合的观点,而是支持门克斯病成纤维细胞中细胞内铜浓度升高导致过量铜与高分子量蛋白质结合,从而刺激铜结合MTP合成的观点。

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