Kelly John J, Stevens Troy, Thompson W Joseph, Seifert Roland
College of Medicine, University of South Alabama, Mobile, AL, USA.
Curr Protoc Pharmacol. 2005 Oct;Chapter 2:Unit2.2. doi: 10.1002/0471141755.ph0202s30.
This unit presents two basic protocols to determine adenylyl cyclase and guanylyl cyclase activity in tissue and cell homogenates, permeabilized cells, or subcellular fractions. Each method is divided into two parts: the enzyme reaction that causes the formation of the labeled cyclic nucleotide, and the separation of cyclic nucleotide products from unreacted nucleotide triphosphates and metabolites using Dowex 50 resin and aluminum oxide chromatographies. In the case of guanylyl cyclase, alternative separation protocols are also provided. Additionally, protocols are provided that describe preparation of both the columns used in the assays and the tissue or cells to be assayed.
本单元介绍了两种基本方案,用于测定组织和细胞匀浆、透化细胞或亚细胞组分中的腺苷酸环化酶和鸟苷酸环化酶活性。每种方法分为两部分:导致标记环核苷酸形成的酶反应,以及使用Dowex 50树脂和氧化铝色谱法从未反应的核苷酸三磷酸和代谢物中分离环核苷酸产物。对于鸟苷酸环化酶,还提供了替代的分离方案。此外,还提供了方案,描述了测定中使用的柱子以及待测组织或细胞的制备方法。