Barrett J C, Crawford B D, Ts'o P O
Cancer Res. 1977 Apr;37(4):1182-5.
Tritium-labeled fibrinogen with a specific activity of 2.0 X 10(7) cpm/mg was prepared by the method of reductive alkylation. The use of the 3H-fibrinogen as a substrate for detection of both intracellular and extracellular fibrinolytic activity derived from cultures of benzo(a)pyrene-transformed Syrian hamster cell lines was examined in cell-free assays, 3H-fibrinogen enabled reliable quantitation of the fibrinolytic activity associated with neoplastic cells. The elevated extracellular fibrinolytic activity in the transformed cell lines as compared to normal hamster embryo cultures was demonstrated with this substrate. The ease with which large quantities of 3H-fibrinogen of high specific activity and prolonged half-life can be prepared makes the use of this substrate an attractive alternative to 125I-labeled fibrinogen.
采用还原烷基化法制备了比活度为2.0×10⁷ cpm/mg的氚标记纤维蛋白原。在无细胞检测中,研究了将³H - 纤维蛋白原用作检测苯并(a)芘转化的叙利亚仓鼠细胞系培养物中细胞内和细胞外纤溶活性的底物,³H - 纤维蛋白原能够可靠地定量与肿瘤细胞相关的纤溶活性。用该底物证明了与正常仓鼠胚胎培养物相比,转化细胞系中细胞外纤溶活性升高。能够制备大量比活度高且半衰期长的³H - 纤维蛋白原,这使得该底物成为¹²⁵I标记纤维蛋白原的有吸引力的替代物。