Von Leoprechting Achim, Kumpf Renate, Menzel Susanne, Reulle Dominique, Griebel Ralf, Valler Martin J, Büttner Frank H
Perkin Elmer LAS (Germany) GmbH, Rodgau-Jügesheim, Germany.
J Biomol Screen. 2004 Dec;9(8):719-25. doi: 10.1177/1087057104268805.
Reducing costs while maintaining the highest readout quality is a precept of modern high-throughput screening. Given the trend toward nonradiometric screening platforms, this has been a big challenge for some kinase target classes. Common issues include low sensitivity, susceptibility to nonspecific interference, or the need for costly reagents. In this study, the authors describe the feasibility of miniaturization of a serine kinase assay using generic reagents in the AlphaScreen format. They have validated the robustness of this assay in the course of miniaturization from a 35-to 4.375-microL final assay volume in 384-and 1536-well formats. Within this volume range, they consistently obtained Z' values above 0.5 and have investigated the suitability of these assay formats for measuring compound effects by testing a set of 25 previously identified active compounds. These active compounds were also reliably identified in the miniaturized assay formats. The results presented here show that the AlphaScreen technology permits robust and cost-efficient miniaturization of serine/threonine kinase assays.
在保持最高读出质量的同时降低成本是现代高通量筛选的一项准则。鉴于非放射性筛选平台的发展趋势,这对某些激酶靶点类别来说一直是个巨大挑战。常见问题包括灵敏度低、易受非特异性干扰,或需要昂贵的试剂。在本研究中,作者描述了使用通用试剂以AlphaScreen形式对丝氨酸激酶检测进行小型化的可行性。他们在从35微升最终检测体积到384孔和1536孔板形式下4.375微升的小型化过程中验证了该检测方法的稳健性。在这个体积范围内,他们始终获得高于0.5的Z'值,并通过测试一组25种先前鉴定的活性化合物研究了这些检测形式对测量化合物效应的适用性。在小型化检测形式中也可靠地鉴定出了这些活性化合物。此处给出的结果表明,AlphaScreen技术允许对丝氨酸/苏氨酸激酶检测进行稳健且经济高效的小型化。