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Sensitivity and Specificity of Plasma Serine Protease Chromogenic Substrates

 

作者: Nils U. Bang,   Lawrence E. Mattler,  

 

期刊: Pathophysiology of Haemostasis and Thrombosis  (Karger Available online 1978)
卷期: Volume 7, issue 2-3  

页码: 98-104

 

ISSN:1424-8832

 

年代: 1978

 

DOI:10.1159/000214244

 

出版商: S. Karger AG

 

关键词: Chromogenic substrates;Thrombin;Plasmin;Kallikrein;Disseminated intravascular coagulation

 

数据来源: Karger

 

摘要:

Rates of hydrolysis of the newly developed peptide chromogenic substrates S-2160, S-2238, S-2222 and S-2251 and Chromozym TH were tested against highly purified preparations of human plasmin, bovine trypsin, human α-thrombin, and bovine factor Xa. S-2160, S-2238, and chromozym TH are sensitive to thrombin, Chromozym TH and S-2238 exhibiting a substantially greater sensitivity than S-2160. All three substrates are insensitive to factor Xa but hydrolyzed to varying degrees by plasmin and trypsin. In contrast, S-2222 is sensitive to factor Xa and insensitive to thrombin. S-2251 is relatively plasmin-specific. In addition, the substrate Chromozym PK was evaluated and found to be relatively specific for plasma kallikrein. Clinically useful assays for antithrombin III and heparin using S-2222 as the substrate and factor Xa as the enzyme, plasma plasminogen and plasmin inhibitors using S-2251 as the substrate, and plasma prekallikrein and kallikrein inhibitors using Chromozym PK as the substrate have been developed

 

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