Nielsen L S, Grøndahl-Hansen J, Andreasen P A, Skriver L, Zeuthen J, Danø K
J Immunoassay. 1986;7(3):209-28. doi: 10.1080/01971528608060467.
A sensitive and specific enzyme-linked immunosorbent assay (ELISA) for human urokinase-type plasminogen activator (u-PA) and its inactive proenzyme (pro-u-PA) was developed. A monoclonal antibody was used as solid-phase antibody, while rabbit antibodies against human u-PA followed by peroxidase-conjugated third antibody were used for detection of bound u-PA. No reaction was observed with tissue-type plasminogen activator or with a variety of other human proteins. The assay was used for quantitation of u-PA in human urine and in culture fluid from human tumor cells. The recovery of added pro-u-PA was greater than 95%. A good agreement with the results obtained by enzymatic assays was found. The detection limit was less than 0.1 ng per ml, both for u-PA and pro-u-PA. The advantages of the use of ELISA compared with enzymatic assays and radioimmunoassays for quantitation of u-PA and pro-u-PA in biological samples are discussed.
开发了一种用于检测人尿激酶型纤溶酶原激活剂(u-PA)及其无活性酶原(pro-u-PA)的灵敏且特异的酶联免疫吸附测定(ELISA)方法。使用单克隆抗体作为固相抗体,同时使用抗人u-PA的兔抗体,随后用辣根过氧化物酶偶联的第三抗体来检测结合的u-PA。未观察到与组织型纤溶酶原激活剂或多种其他人类蛋白质发生反应。该测定法用于定量人尿液和人肿瘤细胞培养液中的u-PA。添加的pro-u-PA回收率大于95%。发现与酶法测定结果具有良好的一致性。u-PA和pro-u-PA的检测限均低于每毫升0.1纳克。讨论了与酶法测定和放射免疫测定相比,使用ELISA定量生物样品中u-PA和pro-u-PA的优势。