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一种提取和纯化肌钙蛋白C的新方法

New method for purification of troponin C

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【作者】 盖晓东丛进阳沈忠耀

【Author】 Gai Xiaodong, Cong Jinyang, Shen Zhongyao (Department of Chemical Engineering, Tsinghua University)

【机构】 清华大学化学工程系!北京100084

【摘要】 肌钙蛋白Ⅰ是肌钙蛋白的一个亚基,它有3种异构体:快、慢骨骼肌肌钙蛋白Ⅰ和心肌肌钙蛋白Ⅰ。由于心肌肌钙蛋白Ⅰ具有极强的心脏特异性,因此引起众多学者的兴趣,研究检测患者血清内心肌肌钙蛋白Ⅰ的含量,来诊断急性心肌梗塞。利用肌钙蛋白C和肌钙蛋白Ⅰ的亲和层析来提取和纯化肌钙蛋白Ⅰ。建立了一种简单的肌钙蛋白C的提取和纯化方法,从兔肌100g中可提取肌钙蛋白C 75mg,不仅高于以往研究结果(60mg/100g兔肌),而且使实验周期缩短和实验操作大为简化。

【Abstract】 Troponin Ⅰ (Tn Ⅰ ) is the inhibitory subunit of troponin. Three isoforms of Tn Ⅰ have been identified: two skeletal Tn Ⅰ isoforms (fast and slow) and one cardiac Tn Ⅰ isoform. Cardiac Tn Ⅰ is suggested to be used for diagnosis of acute myocardial infarction (AMI) by detecting the content of cardiac Tn Ⅰ in patient’s serum because of its specificity for AMI. Cardiac and skeletal Tn Ⅰ were prepared by affinity chromatography using immobilized troponin C (Tn C) in Sepharose-4B as matrix, relying upon the properties of specific Tn C-Tn Ⅰ binding in the presence of calcium. In this paper a new method for purification of Tn C has been introduced with yield of Tn C up to 75 mg/100g rabbit muscle , which is higher than those reported by previous authors. The purification process was much shortened and the procedures were simplified. The preparation of immobilized Tn C Sepharose-4B gel and the purification of Tn Ⅰ were also discussed in detail.

  • 【文献出处】 清华大学学报(自然科学版) ,Journal of Tsinghua University(Science and Technology) , 编辑部邮箱 ,1996年06期
  • 【分类号】TQ464
  • 【被引频次】1
  • 【下载频次】93
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