Owen D G, Jordan C C
J Pharmacol Methods. 1981 Dec;6(4):281-93. doi: 10.1016/0160-5402(81)90068-1.
A modified fluorescence assay for alpha-amylase activity is described. The method employs amylopectin anthranilate as substrate and offers the advantages of economy of time and resources over a previously described technique using the same substrate. The sample containing alpha-amylase is incubated with the substrate for 5 min at 30 degree C in a final volume of 750 microliter. The fluorescent products of the reaction are separated from the substrate by the addition of methanol, and the methanol-soluble fluorescence is measured in a fluorescence spectrometer. A highly reproducible linear relationship between fluorescence and alpha-amylase activity is obtained for enzyme activities up to 2 units. The absolute sensitivity of the assay under these conditions was estimated to be 0.02 EU (= 0.08 EU ml-1). The application of the assay method to a study of the effects of isoprenaline and substance P-like peptides on the release of alpha-amylase from rat parotid gland slices is described. The assay is particularly suitable for studies on agonists, such as substance P, which have a low ceiling effect in terms of amylase release.
本文描述了一种改良的α-淀粉酶活性荧光测定法。该方法采用支链淀粉邻氨基苯甲酸酯作为底物,与先前使用相同底物的技术相比,具有节省时间和资源的优点。将含有α-淀粉酶的样品与底物在30℃下孵育5分钟,最终体积为750微升。通过加入甲醇将反应的荧光产物与底物分离,并在荧光光谱仪中测量甲醇可溶性荧光。对于高达2个单位的酶活性,荧光与α-淀粉酶活性之间获得了高度可重复的线性关系。在这些条件下,该测定法的绝对灵敏度估计为0.02 EU(= 0.08 EU ml-1)。本文描述了该测定方法在研究异丙肾上腺素和P物质样肽对大鼠腮腺切片中α-淀粉酶释放的影响方面的应用。该测定法特别适用于对激动剂(如P物质)的研究,这些激动剂在淀粉酶释放方面具有较低的上限效应。