Schwager Sylva L, Carmona Adriana K, Sturrock Edward D
Division of Medical Biochemistry, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Observatory 7925, South Africa.
Nat Protoc. 2006;1(4):1961-4. doi: 10.1038/nprot.2006.305. Epub 2006 Nov 30.
Angiotensin I-converting enzyme (ACE) assays are commonly used for measuring enzymatic activity in clinical and biological samples. The fluorimetric procedure described is sensitive, rapid and involves unsophisticated procedures and inexpensive reagents. It uses the substrate hippuryl-L-histidyl-L-leucine, and the fluorescent adduct of the enzyme-catalyzed product L-histidyl-L-leucine is quantified fluorimetrically. This assay has been adapted for a 96-well plate format that produces comparable data to previously described assays and has the advantage of greater efficiency with respect to both time and reagents. The protocol can be used for routine purposes or for more detailed kinetic analyses. The apparent Km and kcat values for purified testis ACE determined from a double reciprocal plot were 3.0 mM and 195.7 s(-1), respectively. The protocol can be completed within 4 h.
血管紧张素I转换酶(ACE)测定法常用于临床和生物样本中酶活性的测量。所描述的荧光法灵敏、快速,操作简单且试剂成本低廉。它使用底物马尿酸-L-组氨酸-L-亮氨酸,酶催化产物L-组氨酸-L-亮氨酸的荧光加合物通过荧光法进行定量。该测定法已适用于96孔板形式,可产生与先前描述的测定法相当的数据,并且在时间和试剂方面具有更高的效率优势。该方案可用于常规目的或更详细的动力学分析。从双倒数图确定的纯化睾丸ACE的表观Km和kcat值分别为3.0 mM和195.7 s(-1)。该方案可在4小时内完成。