亲和层析纯化HepG_2细胞分泌的PAI-1  被引量:2

Purification of PAI-1 Secreted from HepG_2 Cell by Immunoaffinity Chromatography

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作  者:丁皓[1] 吴晓俐[1] 孙幼华[1] 周兴华 朱运松[1] 宋后燕[1] 

机构地区:[1]上海医科大学分子遗传研究室

出  处:《生物化学杂志》1994年第1期34-39,共6页

摘  要:本文报道用抗PAI-1单克隆抗体(McAb)亲和层析建立了纯化PAI-1的简便方法。经免疫亲和层析,SephacrylS200凝胶过滤,从HepG2细胞培液中分离到糖基化和非糖基化两种形式的PAI-1,回收率为84%,PAI-1比活性6.1×104IU/mg。糖基化PAI-1分子量为50kD,比活性5.8×104IU/mg。非糖基化PAI-1分子量43kD,占总PAI-130%,仍具有PAI-1活性。用ConA-Sepharose亲和层析进一步纯化得到SDS-PAGE纯的糖基化PAI-1。A simplified procedure for the purification of PAI-1 from HepG2 cell based on immunoaffinity chromatography of anti-PAI-1 monoclonal antibodies(McAbs) was described.After immunoaffinity chromatography and Sephacryl S200 gel filtration, glycoprotein and non-glycoprotein forms of PAI-1 were seperated from HepG2 cell. The yield and the specific activity of putified PAI-1 were 84% and 6.1×104IU/mg, respectively. The MW of glycoprotein form of PAI-1 was about 50kD. The specific activity was 5.8×104IU/mg. The M W of non-glycoprotein form was 43kD. The non-glycoprotein form of PAI-1 contained 30%of total PAI-1 and also had activity of PAI-1. Glycoprotein form of PAI-1 was further purified by ConA-Sepharose chromatography.

关 键 词:PAI-1 纤溶酶原 激活剂抑制物 

分 类 号:Q592.103[生物学—生物化学]

 

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