Moroz L A, Gilmore N J
Blood. 1975 Oct;46(4):543-53.
125I-fibrinogen, adsorbed to polystyrene tubes at low ionic strength and treated with thrombin, serves as a substrate for a rapid, convenient, and sensitive test tube assay for plasmin and activators and inhibitors of this enzyme. 125I-labeled digestion products released from the 125I-fibrin-polystyrene matrix are readily separated and quantitated and behave, on gel permeation, in the same manner as plasmin-generated degradation products from an unlabeled conventional fibrin clot. The 125I-fibrin, in probable non-cross-linked form, is firmly bound to the polystyrene and is resistant to nonspecific release, with control (no enzyme) values equivalent to 15.2 ng +/- 1.2 (SD) fibrin (1% of the total bound 125I-fibrin). This fact permits consistent detection of lysis of 30-50 ng 125I-fibrin, which exceeds published sensitivities (1000-5000 ng) using 125I- or fluorochrome-labeled fibrin clots as substrate. The sensitivity for plasmin (0.2 mug/ml) is tenfold greater than that of the fibrin-plate method (2.0-2.5 mug/ml), while sensitivities for streptokinase and urokinase activation of plasmin are 0.02 U/ml and 0.04 CTA U/ml, respectively (sensitivity of fibrin-plate method, 0.5 U/ml for both). The method provides a reasonable analogue of the solid-phase nature of fibrin under physiologic conditions, and the ease of preparation of large batches of tubes makes the method suitable for large-scale screening of factors modulating the plasminogen-plasmin system.
125I-纤维蛋白原在低离子强度下吸附于聚苯乙烯管,并经凝血酶处理后,可作为纤溶酶及其激活剂和抑制剂的快速、便捷且灵敏的试管检测底物。从125I-纤维蛋白-聚苯乙烯基质释放的125I标记消化产物易于分离和定量,并且在凝胶渗透时的行为与未标记的传统纤维蛋白凝块经纤溶酶产生的降解产物相同。125I-纤维蛋白可能以非交联形式牢固地结合于聚苯乙烯,且抵抗非特异性释放,对照(无酶)值相当于15.2 ng±1.2(标准差)纤维蛋白(占总结合125I-纤维蛋白的1%)。这一事实允许一致地检测30 - 50 ng 125I-纤维蛋白的溶解,其超过了使用125I或荧光染料标记的纤维蛋白凝块作为底物时已发表的灵敏度(1000 - 5000 ng)。对纤溶酶的灵敏度(0.2 μg/ml)比纤维蛋白平板法(2.0 - 2.5 μg/ml)高十倍,而对链激酶和尿激酶激活纤溶酶的灵敏度分别为0.02 U/ml和0.04 CTA U/ml(纤维蛋白平板法对两者的灵敏度均为0.5 U/ml)。该方法在生理条件下提供了纤维蛋白固相性质的合理类似物,并且易于制备大量试管使得该方法适用于大规模筛选调节纤溶酶原-纤溶酶系统的因子。