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纯化基因重组白细胞介素-2的初步研究

Preliminary Study on the Purification of IL-2

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【作者】 阎颖郝茜范国梁赵秋雯刘迎五王建林万冬林

【Author】 YAN Ying\+1, HAO Qian\+1, FAN Guo liang\+1, ZHAO Qiu wen\+1, LIU Ying wu\+2, WANG Jian lin\+2, WAN Dong lin\+2 (1 Analysis Centre of Tianjin University, Tianjin 300072, China; 2 Medical Biotechnical Research Institute, Chinese Medical Fundation,

【机构】 天津大学分析中心!天津300072中国医学基金会医学生物技术研究所!天津300191

【摘要】 采用羟基磷灰石 (HAP)作为填料 ,以pH 6 8的磷酸盐缓冲液为流动相 ,用制备型高效液相色谱来分离提纯基因重组白细胞介素 2 (IL 2 ) ,通过SDS 聚丙烯酰胺凝胶 (SDS PAGE)电泳测定IL 2的纯度 ,测定其活性为1× 1 0 6 U/mg。该法对IL 2的纯化、含量测定及活性测定等效果良好。

【Abstract】 Interleukin 2 (IL 2)which is produced by T lymphocytes is a protein molecule with the molecular weight of 15 420 Daltons. It has good functions in curing a lot of diseases such as cancer and AIDS even with a small quantity A new method for purification of IL 2 by preparative high performance liquid chromatography is described It was the first time to use hydroxyapatite as the packing to separate IL 2 IL 2 has one disulphide bridge (between 58th Cys and 105th Cys )and one free cysteine In order to prevent aggregation and formation of wrong disulphide bond, 50 μmol/L Cu\+\{2+\} and 1 5 mol/L guanidine hydrochloride was used for autoxidation and denaturing Then we used mainly two chromatographic steps: First, Sephadex G 25 Gel permeation chromatography was used to separate guanidine hydrochloride and small molecules Second, large scale preparative HPLC was used to separate impure protein from IL 2 Gradient elution was performed with phosphate buffer (pH 6 8) Its purity was examined by SDS PAGE Its activity reached 1×10\+6 U/mg by CTLL 2 cell MTT method The results showed that it is a suitable method for the large scale purification of IL 2

  • 【文献出处】 色谱 ,CHINESE JOURNAL OF CHROMATOGRAPHY , 编辑部邮箱 ,2000年04期
  • 【分类号】Q78
  • 【被引频次】1
  • 【下载频次】82
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