Scott C F, Kirby E P, Schick P K, Colman R W
Blood. 1981 Mar;57(3):553-60.
The activation of prekallikrein by factor XII fragments (XIIf), during incubation in plastic tubes was previously noted to be increased by high molecular weight (HMW) kininogen as well as other plasma proteins. In this report, we investigated the mechanism responsible for this increase. Although we confirmed that HMW kininogen, bovine serum albumin, fibrinogen, cold insoluble globulin, and mixed phospholipids apparently increased prekallikrein activation, we found that the product of prekallikrein activation (kallikrein) lost substantial activity in less than 0.5 min after exposure to a variety of fresh surfaces. This loss was partially prevented by the presence of various proteins and phospholipids. Similar protection against inactivation of XIIf, the enzyme in this reaction, was also found. In contrast, no loss of the substrate, prekallikrein, was observed during incubation. The loss of kallikrein activity was found to be proportional to the surface area of the incubation vessel as well as the concentration of kallikrein. Further loss of kallikrein activity could also be prevented by pretreating the vessel with kallikrein. We therefore conclude that various substances apparently affect prekallikrein activation in a purified system by preventing the enzyme and product in the reaction mixture from losing activity due to adsorption to a surface.
先前有人指出,在塑料管中孵育期间,因子 XII 片段(XIIf)对前激肽释放酶的激活作用会因高分子量(HMW)激肽原以及其他血浆蛋白而增强。在本报告中,我们研究了导致这种增强的机制。尽管我们证实 HMW 激肽原、牛血清白蛋白、纤维蛋白原、冷不溶性球蛋白和混合磷脂明显增强了前激肽释放酶的激活作用,但我们发现,前激肽释放酶激活产物(激肽释放酶)在暴露于各种新鲜表面后不到 0.5 分钟就失去了大量活性。各种蛋白质和磷脂的存在可部分防止这种活性丧失。在该反应中还发现了对 XIIf(该反应中的酶)失活的类似保护作用。相比之下,在孵育过程中未观察到底物前激肽释放酶的损失。发现激肽释放酶活性的丧失与孵育容器的表面积以及激肽释放酶的浓度成正比。用激肽释放酶预处理容器也可进一步防止激肽释放酶活性的丧失。因此,我们得出结论,在纯化系统中,各种物质显然通过防止反应混合物中的酶和产物因吸附到表面而失去活性来影响前激肽释放酶的激活。