Kool Jeroen, van Liempd Sebastiaan M, van Rossum Huub, van Elswijk Danny A, Irth Hubertus, Commandeur Jan N M, Vermeulen Nico P E
Vrije Universiteit, Department of Pharmacochemistry, LACDR-Division of Molecular Toxicology, De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands.
Drug Metab Dispos. 2007 Apr;35(4):640-8. doi: 10.1124/dmd.106.012245. Epub 2007 Jan 24.
A high resolution screening (HRS) technology is described, in which gradient high-performance liquid chromatography (HPLC) is connected on-line to three parallel placed bioaffinity detection systems containing mammalian cytochromes P450 (P450s). The three so-called enzyme affinity detection (EAD) systems contained, respectively, liver microsomes from rats induced by beta-naphthoflavone (CYP1A activity), phenobarbital (CYP2B activity), and dexamethasone (CYP3A activity). Each P450-EAD system was optimized for enzyme, substrate, and organic modifier (isopropyl alcohol, methanol, and acetonitrile) in flow injection analysis mode. Characteristic P450 ligands were used to validate the P450-EAD systems. IC(50) values of the ligands were measured and found to be similar to those obtained with conventional microtiter plate reader assays. Detection limits (n = 3; signal-to-noise ratio = 3) of potent inhibitors ranged from 1 to 3 pmol for CYP1A activity, 4 to 17 pmol for CYP2B activity, and 4 to 15 pmol for CYP3A activity. The three optimized P450-EAD systems were subsequently coupled to gradient HPLC and used to screen compound mixtures for individual ligands. Finally, to increase analysis efficiency, a HRS system was constructed in which all three P450-EAD systems were coupled on-line and in parallel to gradient HPLC. The triple parallelized P450-EAD system was shown to enable rapid profiling of individual components in complex mixtures for inhibitory activity to three different P450s.
本文描述了一种高分辨率筛选(HRS)技术,其中梯度高效液相色谱(HPLC)与三个平行放置的含有哺乳动物细胞色素P450(P450s)的生物亲和检测系统在线连接。这三个所谓的酶亲和检测(EAD)系统分别包含由β-萘黄酮诱导的大鼠肝微粒体(CYP1A活性)、苯巴比妥(CYP2B活性)和地塞米松(CYP3A活性)。每个P450-EAD系统在流动注射分析模式下针对酶、底物和有机改性剂(异丙醇、甲醇和乙腈)进行了优化。使用特征性P450配体来验证P450-EAD系统。测量了配体的IC(50)值,发现其与使用传统微孔板读数器测定法获得的值相似。强效抑制剂的检测限(n = 3;信噪比 = 3)对于CYP1A活性为1至3 pmol,对于CYP2B活性为4至17 pmol,对于CYP3A活性为4至15 pmol。随后将这三个优化的P450-EAD系统与梯度HPLC耦合,并用于筛选化合物混合物中的单个配体。最后,为了提高分析效率,构建了一个HRS系统,其中所有三个P450-EAD系统在线且平行地与梯度HPLC耦合。结果表明,三重并行化的P450-EAD系统能够快速分析复杂混合物中各个成分对三种不同P450的抑制活性。