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免疫亲和层析法纯化单链尿激酶型纤溶酶原激活剂
引用本文:高丽华,胡显文,吴清法,肖成祖,胥照平,张正光.免疫亲和层析法纯化单链尿激酶型纤溶酶原激活剂[J].生物工程学报,2002,18(3):356-359.
作者姓名:高丽华  胡显文  吴清法  肖成祖  胥照平  张正光
作者单位:军事医学科学院生物工程研究所,北京,100071
基金项目:国家高技术研究发展计划项目资助 (No .Z18 0 3 12)~~
摘    要:尿激酶原 (Pro urokinase ,pro UK) ,也称单链尿激酶型纤溶酶原激活剂 (Single chainurokinase typeplasminogenactivator,scu PA) ,与t PA一样是第二代溶栓药物。给药时 ,保持无活性的酶原状态 ,只激活被纤维蛋白吸附的纤溶酶原 ,而对游离的纤溶酶原没有作用 ,即只在血栓表面才能活化转变为双链尿激酶 (Two chainurokinase typeplasminogenactivator,tcu PA或UK) ,因而具有较高的特异性溶血栓作用1 ] 。尿激酶原…

关 键 词:尿激酶原,单克隆抗体,免疫亲和层析,杂交瘤细胞培养,多孔微载体
文章编号:1000-3061(2002)03-0356-04
修稿时间:2001年11月22

Single-chain Urokinase-type Plasminogen Activator (scu-PA) Purification by Immuno-affimity Chromatography
GAO Li-Hua,HU Xian-Wen WU Qing-Fa XIAO Cheng-Zu XU Zhao-Ping ZHANG Zheng-Guang.Single-chain Urokinase-type Plasminogen Activator (scu-PA) Purification by Immuno-affimity Chromatography[J].Chinese Journal of Biotechnology,2002,18(3):356-359.
Authors:GAO Li-Hua  HU Xian-Wen WU Qing-Fa XIAO Cheng-Zu XU Zhao-Ping ZHANG Zheng-Guang
Institution:Institute of Biotechnology, Beijing 100071, China. Lihuagao@hotmail.com
Abstract:The only difference of primary structure between single-chain prourokinase (pro-UK or scu-PA) and two-chain urokinase (UK or tcu-PA) is the cleavage of a single peptide bond (Lys158-Ile159) and transform scu-PA into its active two-chain form. A 13-peptide (Thr-Leu-Arg-Pro-Arg-Phe-Lys-Ile-Ile-Gly-Gly-Glu-Cys), which spans the cleavage peptide bond, was synthesized and linked to KLH (Keyhole limpet hemocyanin). The Balb/c mice were immunized by the conjugated protein with proper adjuvant. According to the Kohler and Milstein's methods, a hybridoma cell line G7 secreting monoclonal antibody specific for scu-PA was obtained. The anti-scu-PA McAb, purified from the supernatant of porous microcarrier hybridoma cell culture, was conjugated to CNBr-activated Sepharose 4B to prepare an immuno-affinity chromatography column. The u-PA was purified only by this affinity column from the supernatant of cultivating the u-PA-producing recombinant CHO cell, the u-PA recovery ratio is 90.4%, the purification factor was about 50, with the specific activity of 1.2 x 10(5) IU/mg, the scu-PA ratio in the u-PA product was 96.3%. Compared to immuno-affinity chromatography, the 3-step process for purifying u-PA (cation-exchange column, gel filtration column and benzamidine affinity column) has a u-PA recovery ratio of about 65%, with a specific activity of 1.0 x 10(5) IU/mg, and an scu-PA ratio of about 90%. These results showed that immuno-affinity chromatography is simple to recover u-PA and effective to separate scu-PA from tcu-PA.
Keywords:prourokinase  monoclonal antibody  immuno-affinity chromatography  hybridoma cell culture  porous microcarrier
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