Department of Bio-analytical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.
Anal Biochem. 2013 Jun 1;437(1):10-6. doi: 10.1016/j.ab.2013.01.023. Epub 2013 Jan 31.
Angiotensin (Ang) II is critically involved in multiple cardiovascular diseases mainly through the Ang II type 1 (AT1) receptor. Thus, AT1 receptor antagonists have been widely used for the treatment of hypertension and other cardiovascular conditions. However, most binding assays for AT1 receptor are based on radioactivity or fluorescent labeling, which present disadvantages such as radioactive waste production and/or changes to the binding characteristics of the labeled receptor or ligand. This article describes the first matrix-assisted laser desorption ionization-time of flight/mass spectrometry (MS)-based label-free binding assay for AT1 receptor that can be performed in a high-throughput format. The affinity of competitors can be directly compared to that of Ang II by quantifying Ang II dissociated from the receptor-ligand complex using 50% methanol in water. The sensitivity and selectivity of MS analysis was improved by employing a stable-isotope ((13)C, (15)N)-labeled internal standard. This assay provided binding results equivalent to those obtained using other methods and revealed a significant decrease in the binding affinity of Ang II when the N-terminus underwent oxidative modification. The current setup of the assay can be easily adapted for other Ang receptors and would facilitate drug discovery studies targeting Ang receptors.
血管紧张素(Ang)II 通过血管紧张素 II 型 1(AT1)受体在多种心血管疾病中起着关键作用。因此,AT1 受体拮抗剂已广泛用于治疗高血压和其他心血管疾病。然而,大多数 AT1 受体的结合测定都是基于放射性或荧光标记,这存在放射性废物产生和/或标记的受体或配体结合特性发生变化等缺点。本文描述了第一个基于基质辅助激光解吸电离飞行时间/质谱(MS)的无标签 AT1 受体结合测定法,可进行高通量测定。通过使用 50%甲醇在水中定量从受体-配体复合物中解离的 Ang II,可以直接比较竞争物的亲和力与 Ang II 的亲和力。通过使用稳定同位素((13)C,(15)N)标记的内标,提高了 MS 分析的灵敏度和选择性。该测定法提供了与其他方法获得的测定结果相当的结果,并显示当 N 末端发生氧化修饰时,Ang II 的结合亲和力显着降低。该测定法的当前设置可以很容易地适应其他 Ang 受体,并将促进针对 Ang 受体的药物发现研究。