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机构地区:[1]北京江中药物研究所,北京100050 [2]解放军军需大学军事兽医研究所,吉林长春130062
出 处:《中国兽医学报》2000年第3期235-238,共4页Chinese Journal of Veterinary Science
摘 要:对转基因山羊乳腺定位表达的羊奶中组织型纤维蛋白溶酶原激活剂 ( t PA)的分离纯化方法作了研究 ,摸索出一种简单可行的纯化方法。羊奶中 t PA先经冰乙酸和丙酮沉淀后 ,再通过 Benzamidin Sepharose 6B柱一步亲和层析 ,纯化倍数达 671 4.3倍 ,比活性 1 880 0 0 U/mg,活性回收率 2 6%。经 SDS-PAGE还原电泳分析 ,t PA纯度大于 95%,其中低分子双链蛋白占 90 %以上 ;Western-blotting检测证实 ,它和天然 t PA具有相同的抗原性 ;用纤维蛋白平板法检测 ,其比活性与天然 t PA相近 ,并且都可被 tA tissue type plasminogen activator derived from expression by milk gland of transgenic goat was isolated and purificated. Precipitated with acetate acid and acetone in advance, the t PA in the milk was purificated using one step affinity chromatography with benzamidin sepharose 6B. The final product had a specific activity of 188 000 IU/mg protein. The overall activity recovery was about 26% with 6 714.3 fold increase in specific activity. Analysis by SDS PAGE electrophoresis in the presence of a reducing agent, the purity of t PA was over 95% with the two chain t PA to be occupied over 90% of it. Western blotting analysis showed that the product was possessed of the natural t PA antigen characteristics. Analysed with fibrin plate, the product had the same specific activity and molecular weight as natural t PA and could be inhibited by the t PA monoclonal antibody.
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