Willemse Johan L, Hendriks Dirk F
Laboratory of Medical Biochemistry, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Antwerp, Belgium.
Clin Chim Acta. 2006 Sep;371(1-2):124-9. doi: 10.1016/j.cca.2006.02.035. Epub 2006 Apr 17.
Carboxypeptidase N is a plasma zinc metallocarboxypeptidase which is constitutively expressed in the liver and was identified as the enzyme responsible for inactivating bradykinin and kallidin by removing the C-terminal arginine. Because CPN can cleave the C-terminal arginine of C3a, C4a and C5a it is often referred to as anaphylatoxin inactivator. Markedly reduced levels of circulating CPN are associated with recurrent angioedema and abnormal cutaneous polymorphonuclear cell infiltration.
In this paper we describe a fast kinetic coupled enzymatic assay for the sensitive measurement of carboxypeptidase N activities in serum samples. The assay makes use of the excellent CPN substrate Benzoyl-L-Alanyl-L-Arginine.
This novel assay is very fast, easy to perform and combines good reliability and reproducibility with excellent correlation with the HPLC-assisted assay (r=0.927; n=140).
The presented assay can be used for high throughput screening of this important regulator of inflammation in clinical plasma or serum samples.
羧肽酶N是一种血浆锌金属羧肽酶,在肝脏中组成性表达,被确定为通过去除C末端精氨酸来使缓激肽和胰激肽失活的酶。由于CPN可以切割C3a、C4a和C5a的C末端精氨酸,它常被称为过敏毒素灭活剂。循环CPN水平显著降低与复发性血管性水肿和异常皮肤多形核细胞浸润有关。
在本文中,我们描述了一种快速动力学偶联酶法,用于灵敏测量血清样本中的羧肽酶N活性。该测定法使用了出色的CPN底物苯甲酰-L-丙氨酰-L-精氨酸。
这种新型测定法速度非常快,易于操作,具有良好的可靠性和可重复性,与HPLC辅助测定法具有出色的相关性(r=0.927;n=140)。
所提出的测定法可用于临床血浆或血清样本中这种重要炎症调节剂的高通量筛选。