Sausen Christopher W, Rogers Cody M, Bochman Matthew L
Department of Molecular and Cellular Biochemistry, Indiana University, Bloomington, IN, USA.
Methods Mol Biol. 2019;1999:245-253. doi: 10.1007/978-1-4939-9500-4_15.
Many chemical reactions in the cell are thermodynamically unfavorable. To overcome this barrier, the energy released from the hydrolysis of adenosine triphosphate (ATP) is coupled to these reactions via ATP hydrolyzing enzymes known as ATPases. These enzymes are ubiquitous in nature and frequently act as molecular motors in processes ranging from DNA replication to protein degradation. Assays that characterize ATPase activity in vitro are important tools to gain insight into their functions in vivo. Here, we describe a direct and flexible thin-layer chromatography method for detecting ATPase activity using radiolabeled ATP. Additionally, we describe a high-throughput coupled reaction assay pairing ATP hydrolysis with nicotinamide adenine dinucleotide (NADH) oxidation to monitor ATP hydrolysis in real time.
细胞内的许多化学反应在热力学上是不利的。为了克服这一障碍,三磷酸腺苷(ATP)水解所释放的能量通过被称为ATP酶的ATP水解酶与这些反应偶联。这些酶在自然界中无处不在,并且在从DNA复制到蛋白质降解等一系列过程中经常充当分子马达。在体外表征ATP酶活性的测定方法是深入了解其体内功能的重要工具。在这里,我们描述了一种使用放射性标记的ATP来检测ATP酶活性的直接且灵活的薄层色谱法。此外,我们还描述了一种高通量偶联反应测定法,该方法将ATP水解与烟酰胺腺嘌呤二核苷酸(NADH)氧化配对,以实时监测ATP水解。