Cali James J, Ma Dongping, Sobol Mary, Simpson Daniel J, Frackman Susan, Good Troy D, Daily William J, Liu David
Promega Corp., Madison, WI 53711, USA.
Expert Opin Drug Metab Toxicol. 2006 Aug;2(4):629-45. doi: 10.1517/17425255.2.4.629.
Luminogenic cytochrome P450 (CYP) assays couple CYP enzyme activity to firefly luciferase luminescence in a technology called P450-Glo(TM) (Promega). Luminogenic substrates are used in assays of human CYP1A1, -1A2, -1B1, -2C8, -2C9, -2C19, -2D6, -2J2, -3A4, -3A7, -4A11, -4F3B, -4F12 and -19. The assays detect dose-dependent CYP inhibition by test compounds against recombinant CYP enzymes or liver microsomes. Induction or inhibition of CYP activities in cultured hepatocytes is measured in a nonlytic approach that leaves cells intact for additional analysis. Luminogenic CYP assays offer advantages of speed and safety over HPLC and radiochemical-based methods. Compared with fluorogenic methods the approach offers advantages of improved sensitivity and decreased interference between optical properties of test compound and CYP substrate. These homogenous assays are sensitive and robust tools for high-throughput CYP screening in early drug discovery.
发光细胞色素P450(CYP)检测法通过一种名为P450-Glo™(普洛麦格公司)的技术,将CYP酶活性与萤火虫荧光素酶发光相偶联。发光底物用于检测人CYP1A1、-1A2、-1B1、-2C8、-2C9、-2C19、-2D6、-2J2、-3A4、-3A7、-4A11、-4F3B、-4F12和-19。这些检测法可检测受试化合物对重组CYP酶或肝微粒体的剂量依赖性CYP抑制作用。采用非裂解方法测量培养肝细胞中CYP活性的诱导或抑制情况,使细胞保持完整以便进行进一步分析。与基于高效液相色谱(HPLC)和放射化学的方法相比,发光CYP检测法具有速度快和安全性高的优点。与荧光法相比,该方法具有灵敏度提高、受试化合物与CYP底物光学性质之间干扰减少的优点。这些均相检测法是早期药物发现中高通量CYP筛选的灵敏且可靠的工具。