Sugo T, Ohno Y, Shimada T, Kato H, Iwanaga S
Adv Exp Med Biol. 1983;156:87-107.
The mechanism of kaolin-mediated activation of bovine Factor XII was studied in the presence of prekallikrein and HMW kininogen. The activated enzymes were assayed using fluorogenic peptides, Boc-Glu (OBzl)-Gly-Arg-4-methylcoumaryl-7-amide (MCA) for Factor XIIa and Z-Phe-Arg-MCA for plasma kallikrein. The rates of activation of the zymogens were separately measured by blocking either of the active enzymes with specific inhibitors, corn inhibitor for Factor XIIa (Ki = 6.7 nM) and Trasylol for plasma kallikrein (Ki = 3.9 nM). The result was as follows: (1) At the early stage of the activation reaction, kallikrein activity was first generated after short lag time, and then Factor XIIa activity was generated with a sigmoidal curve. In the presence of corn inhibitor, the activation of prekallikrein was observed, but in the presence of Trasylol, the activation of Factor XII was not observed. In the presence of high concentration of Ala-Phe-Arg-Ch2Cl, which inactivates immediately both of the active enzymes, the cleavage of a single chain prekallikrein into the two chain form by Factor XII was shown by SDS-PAGE, using nonlabelled and tritiated prekallikrein. (2) The incubation of Factor XII alone in a quartz cuvette or in the presence of kaolin and HMW kininogen did not result in the activation of Factor XII. The concave upward curve due to an autocatalytic activation was not observed even after the addition of Factor XIIa to Factor XII preparation. Moreover, no structural change of Factor XII during the incubation with kaolin and HMW kininogen was shown by SDS-PAGE, using 3H-Factor XII. (3) The rates of activation of prekallikrein by Factor XII and by Factor XIIa were approximately the same at higher concentration of prekallikrein. However, at lower concentration of prekallikrein the rate of activation of prekallikrein by Factor XII was shown to be a sigmoidal curve and slower than that by Factor XIIa. These results indicate that the activation of bovine Factor XII is initiated by the attack of Factor XII on prekallikrein, followed by the reciprocal activation of Factor XII by plasma kallikrein generated. The autocatalytic activation of bovine Factor XII by Factor XIIa was not demonstrated.
在存在前激肽释放酶和高分子量激肽原的情况下,研究了高岭土介导的牛因子XII激活机制。使用荧光肽对活化的酶进行测定,用于因子XIIa的是Boc-Glu(OBzl)-Gly-Arg-4-甲基香豆素-7-酰胺(MCA),用于血浆激肽释放酶的是Z-Phe-Arg-MCA。通过用特异性抑制剂阻断其中一种活性酶来分别测量酶原的活化速率,用于因子XIIa的是玉米抑制剂(Ki = 6.7 nM),用于血浆激肽释放酶的是抑肽酶(Ki = 3.9 nM)。结果如下:(1)在活化反应的早期阶段,激肽释放酶活性在短暂的延迟时间后首先产生,然后因子XIIa活性呈S形曲线产生。在存在玉米抑制剂的情况下,观察到前激肽释放酶的活化,但在存在抑肽酶的情况下,未观察到因子XII的活化。在存在高浓度的Ala-Phe-Arg-Ch2Cl(其可立即使两种活性酶失活)的情况下,使用未标记和氚标记的前激肽释放酶,通过SDS-PAGE显示因子XII将单链前激肽释放酶切割成两条链的形式。(2)单独在石英比色皿中或在存在高岭土和高分子量激肽原的情况下孵育因子XII,不会导致因子XII的活化。即使在向因子XII制剂中添加因子XIIa后,也未观察到由于自催化活化而产生的向上凹的曲线。此外,使用3H-因子XII的SDS-PAGE显示,在与高岭土和高分子量激肽原孵育期间,因子XII没有结构变化。(3)在较高浓度的前激肽释放酶下,因子XII和因子XIIa对前激肽释放酶的活化速率大致相同。然而,在较低浓度的前激肽释放酶下,因子XII对前激肽释放酶的活化速率呈S形曲线,且比因子XIIa慢。这些结果表明,牛因子XII的活化是由因子XII攻击前激肽释放酶引发的,随后由产生的血浆激肽释放酶对因子XII进行相互活化。未证明因子XIIa对牛因子XII的自催化活化。