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使用新型蛋白C激活剂Protac进行快速功能性蛋白C检测。

Fast functional protein C assay using Protac, a novel protein C activator.

作者信息

Martinoli J L, Stocker K

出版信息

Thromb Res. 1986 Aug 1;43(3):253-64. doi: 10.1016/0049-3848(86)90145-3.

Abstract

A simple and rapid clotting method for the quantitative determination of protein C (PC) in plasma consists of the conversion of PC into activated PC (APC) by means of Protac, an activator protein isolated from Agkistrodon contortrix contortrix venom, of the subsequent degradation of factors V and VIII in PC immuno-depleted plasma by the generated APC and of the measurement of the prolongation of the activated partial thromboplastin time (APTT) which is proportional to the amount of PC in the sample. In 33 normal individuals a mean PC level of 97.1% of a normal pooled plasma was found. Comparison with an enzyme-immunoassay for PC in 33 patients with liver disease revealed a good correlation (r = 0.986). Patients under warfarin therapy (n = 34) had a mean PC level of 19.8%; a comparison with the immunological assay (mean value = 55.3%) in the same population suggested that the assay did not co-estimate acarboxy forms of PC. The assay proved to be insensitive to heparin concentration lower than 1 U/ml. Due to its simplicity, it should be suitable for diagnostic routine and monitoring of patients with abnormal PC level, even if under anticoagulation.

摘要

一种用于定量测定血浆中蛋白C(PC)的简单快速凝血方法,包括通过Protac(一种从五步蛇毒液中分离出的激活蛋白)将PC转化为活化蛋白C(APC),随后生成的APC使PC免疫耗尽血浆中的因子V和VIII降解,并测量活化部分凝血活酶时间(APTT)的延长,该延长与样品中PC的量成正比。在33名正常个体中,发现PC水平平均为正常混合血浆的97.1%。对33名肝病患者进行PC酶免疫测定的比较显示出良好的相关性(r = 0.986)。接受华法林治疗的患者(n = 34)的PC水平平均为19.8%;与同一人群中的免疫测定(平均值 = 55.3%)比较表明,该测定未共同估计PC的无羧基形式。该测定被证明对低于1 U/ml的肝素浓度不敏感。由于其简单性,它应该适用于诊断常规以及监测PC水平异常的患者,即使在抗凝治疗下也是如此。

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