Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
Nat Protoc. 2010 Jun;5(6):1107-14. doi: 10.1038/nprot.2010.47. Epub 2010 May 27.
The identification of new antifungal molecules is an important goal of current anti-infective research. To achieve this goal, alternatives to traditional growth inhibition-based screening have been developed in recent years. In this study, we describe an assay to detect molecules that disrupt yeast cell integrity by using the release of adenylate kinase (AK) into culture medium as a reporter of yeast cell lysis. The protocol is applicable to 96- and 384-well microtiter plate formats; uses a commercially available luminescence assay kit to detect AK activity; is more sensitive than traditional growth-based assays; and is specific for fungicidal compounds. In the high-throughput setting, the procedure provides excellent Z' scores (0.75-0.9), making it a highly robust assay. The AK assay is performed in a single microtiter plate using an 'add and read' procedure that can be completed in a single work day.
鉴定新的抗真菌分子是当前抗感染研究的一个重要目标。近年来,为了实现这一目标,已经开发出了替代传统基于生长抑制的筛选方法。在这项研究中,我们描述了一种通过检测细胞内腺苷酸激酶(AK)释放到培养基中,来检测破坏酵母细胞完整性的分子的方法。该方案适用于 96 孔和 384 孔微量滴定板格式;使用市售的发光测定试剂盒检测 AK 活性;比传统的基于生长的测定方法更灵敏;并且特异性针对杀真菌化合物。在高通量设置中,该程序提供了极好的 Z'分数(0.75-0.9),使其成为一种非常稳健的测定方法。AK 测定是在单个微量滴定板中进行的,采用“添加和读取”程序,可在一个工作日内完成。