Iyamu Efewmonkiekie W, Asakura Toshio, Woods Gerald M
Division of Hematology and Oncology, Children's Mercy Hospital, University of Missouri Medical Center, Kansas City, MO 64108, USA.
Anal Biochem. 2008 Dec 15;383(2):332-4. doi: 10.1016/j.ab.2008.08.016. Epub 2008 Aug 23.
Several analytical methods have been developed for the determination of arginase (l-arginine amidinohydrolase) activity in physiological samples. These methods are limited by the considerable effort and time required to obtain reliable and reproducible measurements. Here we describe a simple high-throughput colorimetric assay for the determination of arginase activity based on the ornithine-ninhydrin reaction. This method is an improvement over the original single cuvette assay developed by Chinard in that no boiling step is required. The turnaround time has been reduced, with improved precision and reproducibility. The method was extended to the determination of arginase activity in human leukemic (K562) cells and sickle erythrocytes. We believe that the method will find applications for routine analysis as well as for characterizing the action of novel and potent inhibitors on arginase activity.
已经开发了几种分析方法用于测定生理样品中的精氨酸酶(L-精氨酸脒基水解酶)活性。这些方法受到获得可靠且可重复测量所需的大量精力和时间的限制。在此,我们描述了一种基于鸟氨酸-茚三酮反应测定精氨酸酶活性的简单高通量比色法。该方法是对Chinard开发的原始单比色皿测定法的改进,因为不需要煮沸步骤。周转时间缩短,精度和重现性提高。该方法扩展到了人白血病(K562)细胞和镰状红细胞中精氨酸酶活性的测定。我们相信该方法将在常规分析以及表征新型强效抑制剂对精氨酸酶活性的作用方面找到应用。