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人唾液激肽释放酶的特性:对人血浆激肽原和蛋白酶抑制剂的反应性

Characterization of human salivary kallikrein: reactivities to human plasma kininogens and proteinase inhibitors.

作者信息

Sakamoto W, Yoshikawa K, Uehara S, Nishikaze O

出版信息

J Biochem. 1983 Mar;93(3):833-8. doi: 10.1093/jb/93.3.833.

Abstract

In order to clarify the enzymatic properties of human salivary kallikrein, we investigated its actions on human plasma kininogens and response to proteinase inhibitors. Salivary kallikrein released kinin from both LMW and HMW kininogens, but acted preferentially on LMW kininogen. Salivary kallikrein did not completely release the kinin from HMW kininogen even after prolonged incubation (up to 60 min). The kinin releasing activity of salivary kallikrein was not inhibited by plasma proteinase inhibitors such as alpha 2M, alpha 2PI, AT III, and C1 INA after preincubation for 60 min at 37 degrees C, but was inhibited progressively by alpha 1AT as a function of preincubation time. SDS-PAGE revealed that concomitantly with the progressive inhibition a new band of 92,000 daltons, which seemed to be a complex of salivary kallikrein and alpha 1AT, was produced. The kininogen-depleted plasma inhibited the salivary kallikrein to the same degree as alpha 1AT. Therefore, it is suggested that alpha 1AT is the only inhibitor of salivary kallikrein in human plasma.

摘要

为了阐明人唾液激肽释放酶的酶学特性,我们研究了其对人血浆激肽原的作用以及对蛋白酶抑制剂的反应。唾液激肽释放酶可从低分子量(LMW)和高分子量(HMW)激肽原中释放激肽,但对LMW激肽原的作用更为优先。即使经过长时间孵育(长达60分钟),唾液激肽释放酶也不能从HMW激肽原中完全释放激肽。在37℃预孵育60分钟后,唾液激肽释放酶的激肽释放活性不受血浆蛋白酶抑制剂如α2M、α2PI、抗凝血酶III(AT III)和C1酯酶抑制剂(C1 INA)的抑制,但会随着预孵育时间的延长而被α1抗胰蛋白酶(α1AT)逐渐抑制。十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)显示,随着抑制作用的逐渐增强,产生了一条92,000道尔顿的新条带,它似乎是唾液激肽释放酶和α1AT的复合物。激肽原缺乏的血浆对唾液激肽释放酶的抑制程度与α1AT相同。因此,提示α1AT是人类血浆中唾液激肽释放酶的唯一抑制剂。

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