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A high-throughput assay of yeast cell lysis for drug discovery and genetic analysis.

机译:酵母细胞裂解的高通量分析,用于药物发现和遗传分析。

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摘要

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.
机译:新的抗真菌分子的鉴定是当前抗感染研究的重要目标。为了实现这一目标,近年来已经开发了传统的基于生长抑制的筛选方法。在这项研究中,我们描述了一种检测方法,该方法通过使用腺苷酸激酶(AK)释放到培养基中作为酵母细胞裂解的报告基因来检测破坏酵母细胞完整性的分子。该协议适用于96和384孔微量滴定板规格;使用市售的发光分析试剂盒检测AK活性;比传统的基于生长的测定法更敏感;对杀真菌化合物具有特异性。在高通量环境中,该程序可提供出色的Z'分数(0.75-0.9),使其成为高度可靠的测定方法。使用“添加和读取”程序在单个微量滴定板上进行AK测定,该步骤可以在一个工作日内完成。

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