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重组刺桐胰蛋白酶抑制剂的复性纯化
Refolding and Purification of Erythrina Trypsin Inhibitor
【摘要】 刺桐胰蛋白酶抑制剂(ETI)是一种丝氨酸蛋白酶抑制剂,可抑制胰蛋白酶、胰凝乳蛋白酶及组织纤溶酶原激活剂(t-PA)等。本研究利用大肠杆菌高密度发酵表达ETI,产物以包涵体形式存在,经体外以脉冲稀释的方式复性并纯化后,每升发酵液可得ETI1000mg以上,纯度大于95%,比活为1.55IU/mg。ETI制成的ETI-Sepharose亲和胶,每ml可吸附重组瑞特普酶融合蛋白(Trx-rPA)2mg,可应用于制备t-PA及其衍生物如r-PA等药用蛋白。
【Abstract】 Erythrina trypsin inhibitor (ETI) is a natural serine protease inhibitor, with high inhibitive activity to trypsin, chemotrypsin and tissue-type plasminogen activator (t-PA). In this work, ETI was over expressed as inclusion bodies in high density fermentation of E. coli. By means of pulse refolding and two-step purification, over 1000 mg of ETI was obtained from one litre of culture. Its purity was over 95% , and specific activity 1.55 IU/mg. ETI, immobilized on Sepharose with high binding capacity of the recombinant fusion protein Trx-rPA up to 2 mg/ml gel, is a promising choice for purifying t-PA and its derivatives such as r-PA .
【Key words】 Erythrina trypsin inhibitor; refolding; tissue-type plasminogen activator; reteplase;
- 【文献出处】 中国医药工业杂志 ,Chinese Journal of Pharmaceuticals , 编辑部邮箱 ,2007年05期
- 【分类号】Q814
- 【被引频次】1
- 【下载频次】113