Blackmon D L, Watson A J, Montrose M H
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Anal Biochem. 1992 Feb 1;200(2):352-8. doi: 10.1016/0003-2697(92)90478-p.
A series of enzymatic rate assays are described. The assays are based on coumarin derivatives that are fluorogenic substrates for the enzymes dipeptidase IV, aminopeptidase N, alkaline phosphatase, and gamma-glutamyltransferase. These simple assays are rapid and offer improved sensitivity over established colorimetric methods. The substrates have apparent affinities for the enzymes of 5-250 microM. L-Glutamic acid gamma-(7-amido-4-methylcoumarin) is characterized as a substrate of gamma-glutamyltransferase on the basis of inhibition of enzymatic cleavage when the glycylglycine acceptor molecule is omitted and inhibition of the enzymatic reaction by addition of glycine. Assay conditions for the four enzymes are established such that less than 0.6% of the substrate is consumed, fluorescence is proportional to enzymatic product, and results may be directly compared to established colorimetric assays. Intestinal epithelial cells are used both to establish appropriate assay conditions and to demonstrate the utility of the assays.
本文描述了一系列酶促速率测定方法。这些测定基于香豆素衍生物,它们是二肽酶IV、氨肽酶N、碱性磷酸酶和γ-谷氨酰转移酶的荧光底物。这些简单的测定方法快速,并且与已有的比色法相比具有更高的灵敏度。这些底物对酶的表观亲和力为5-250微摩尔。L-谷氨酸γ-(7-氨基-4-甲基香豆素)被表征为γ-谷氨酰转移酶的底物,这是基于当省略甘氨酰甘氨酸受体分子时酶促裂解受到抑制以及添加甘氨酸会抑制酶促反应。确定了四种酶的测定条件,使得消耗的底物少于0.6%,荧光与酶促产物成比例,并且结果可以直接与已有的比色法进行比较。使用肠上皮细胞来确定合适的测定条件并证明这些测定方法的实用性。