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血浆前羧肽酶U的快速均相测定法。

Fast homogeneous assay for plasma procarboxypeptidase U.

作者信息

Schatteman K A, Goossens F J, Leurs J, Kasahara Y, Scharpé S S, Hendriks D F

机构信息

Department of Medical Biochemistry, University of Antwerp, Wilrijk, Belgium.

出版信息

Clin Chem Lab Med. 2001 Sep;39(9):806-10. doi: 10.1515/CCLM.2001.133.

Abstract

Carboxypeptidase U (EC 3.4.17.20, CPU, TAFIa) is a novel determinant of the fibrinolytic rate. It circulates as an inactive zymogen, procarboxypeptidase U, which becomes active during the process of coagulation. We developed a high throughput method on microtiter plates for the determination of the procarboxypeptidase U concentration in human plasma samples. Following activation of procarboxypeptidase U by thrombin-thrombomodulin, the resulting enzyme activity cleaves p-OH-Hip-Arg and the generated p-OH-hippuric acid is converted by hippuricase to p-hydroxybenzoic acid and glycine. Finally, oxidative coupling of p-hydroxybenzoic acid with 4-aminoantipyrine by NaIO4 forms the quinoneimine dye. The absorbance of the latter dye is determined at 506 nm in a microtiter plate reader. A mean value of 620 U/l was found, with a CV of 3.0% within-run and 4.3% between-run. The assay showed a good correlation with the activities observed using a HPLC assay as reference method (n = 25, r = 0.979). The presented method enables the routine analysis of large sample pools in clinical setting.

摘要

羧肽酶U(EC 3.4.17.20,CPU,TAFIa)是纤维蛋白溶解速率的一个新的决定因素。它以无活性的酶原——羧肽酶原U的形式循环,在凝血过程中被激活。我们开发了一种在微量滴定板上的高通量方法,用于测定人血浆样本中羧肽酶原U的浓度。在凝血酶-血栓调节蛋白激活羧肽酶原U后,产生的酶活性裂解对羟基苯甲酰精氨酸,生成的对羟基马尿酸被马尿酸酶转化为对羟基苯甲酸和甘氨酸。最后,高碘酸钠使对羟基苯甲酸与4-氨基安替比林发生氧化偶联,形成醌亚胺染料。在微量滴定板读数仪中于506 nm处测定后一种染料的吸光度。发现平均值为620 U/l,批内变异系数为3.0%,批间变异系数为4.3%。该测定方法与以HPLC测定法作为参考方法观察到的活性具有良好的相关性(n = 25,r = 0.979)。所提出的方法能够在临床环境中对大量样本进行常规分析。

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