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大鼠肝脏金属硫蛋白的分离纯化和金属硫蛋白亚型-Ⅱα结构域片段的制备及其核磁共振鉴定

Separation and Purification of Rat Liver Metallothionein, Preparation of α-Domain Fragments of MT- Ⅱ and Their Characterization by NMR

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【作者】 黄仲贤顾伟强胡红雨王韵华

【Author】 HUANG Zhong-Xian , GU Wei-Qiang, HU Hong-Yu, WANG Yun-Hua (Department of Chemistry, Fudan University, Shanghai, 200433)

【机构】 复旦大学化学系复旦大学化学系 上海 200433上海 200433上海 200433

【摘要】 Wistar雄性大鼠经腹腔注射CdCl2诱导其肝脏合成金属硫蛋白。取鼠肝,先经匀浆、热变性、乙醇-氯仿萃取、丙酮沉淀等步骤,后由Sephadex G-75、DEAE-52柱层析,得金属硫蛋白的两亚型Ⅰ和Ⅱ。经原子吸收光谱测定每蛋白分子含有5个镉和2个锌。用枯草杆菌酶割法制备并分离了金属硫蛋白亚型Ⅱ的α结构域片段。还用NMR研究了金属硫蛋白的两个亚型及所得的α结构域片段。

【Abstract】 The rat liver metallothionein was induced by administering 7 subcutaneous injection of CdCl2 to the wistar rat. The purification protocal involved homogenization of rat liver, heating, extraction by ethanol-chloroform, acetone precipitation, and finally, chromatography on Sephadex G-75 and DEAE-52 columns. Two isoforms of metallothionein, Cd5Zn2-MT- Ⅰ and -Ⅱ , with A250/ A250> 20 were obtained. MT- Ⅱα domain fragment containing four cadmium ions was also isolated by digestion with subtilysin. 1H NMR spectra of MT- Ⅰ , - Ⅱ were in agreement with those reported in literatures. The spectrum of MT- Ⅰ α domain shows that there is no existence of β fragment in this preparation.

【基金】 国家自然科学基金
  • 【文献出处】 高等学校化学学报 ,Chemical Research In Chinese Universities , 编辑部邮箱 ,1993年04期
  • 【被引频次】7
  • 【下载频次】86
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