Hammond Edward, Ferro Vito
Zucero Therapeutics, Brisbane, QLD, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
Methods Mol Biol. 2023;2619:227-238. doi: 10.1007/978-1-0716-2946-8_16.
The enzyme heparanase cleaves heparan sulfate and is involved in a range of human diseases including cancer, inflammation, diabetes, and viral infection. There is a need for a simple and reliable enzymatic assay to allow for the screening of compounds to find inhibitors of heparanase. We have developed an assay that uses the heparinoid fondaparinux as enzyme substrate and detects one of the products of catalysis, which contains a newly formed reducing terminus, with the tetrazolium salt WST-1. Due to the homogenous substrate and single point of cleavage therein, this assay allows for more systematic kinetic analysis of heparanase inhibitors. Here, we provide a detailed method for conducting this assay and also provide information to assist researchers in evaluating whether the assay is performing properly in their laboratories.
乙酰肝素酶可切割硫酸乙酰肝素,参与包括癌症、炎症、糖尿病和病毒感染在内的一系列人类疾病。需要一种简单可靠的酶促测定法,以便筛选化合物来寻找乙酰肝素酶抑制剂。我们开发了一种测定法,该方法使用类肝素药物磺达肝癸钠作为酶底物,并利用四唑盐WST-1检测催化产物之一,该产物含有新形成的还原末端。由于底物均匀且其中只有一个切割位点,该测定法能够对乙酰肝素酶抑制剂进行更系统的动力学分析。在此,我们提供了进行该测定的详细方法,并提供信息以帮助研究人员评估该测定法在其实验室中是否正常运行。