Bray Walter, Lokey R Scott
Department of Chemistry and Biochemistry, University of California Santa Cruz, Santa Cruz, California 95064.
Cold Spring Harb Protoc. 2016 Sep 1;2016(9):2016/9/pdb.prot088047. doi: 10.1101/pdb.prot088047.
When a disk of filter paper is impregnated with a cytotoxic or cytostatic drug and added to solid medium seeded with yeast, a visible clear zone forms around the disk whose size depends on the concentration and potency of the drug. This is the traditional "halo" assay and provides a convenient, if low-throughput, read-out of biological activity that has been the mainstay of antifungal and antibiotic testing for decades. Here, we describe a protocol for a high-throughput version of the halo assay, which uses an array of 384 pins to deliver ∼200 nL of stock solutions from compound plates onto single-well plates seeded with yeast. Using a plate reader in the absorbance mode, the resulting halos can be quantified and the data archived in the form of flat files that can be connected to compound databases with standard software. This assay has the convenience associated with the visual readout of the traditional halo assay but uses far less material and can be automated to screen thousands of compounds per day.
当用细胞毒性或细胞抑制药物浸渍滤纸圆盘,并将其添加到接种酵母的固体培养基中时,圆盘周围会形成一个可见的清晰区域,其大小取决于药物的浓度和效力。这就是传统的“晕圈”试验,它提供了一种方便的(尽管通量较低)生物活性读数,几十年来一直是抗真菌和抗生素测试的主要方法。在这里,我们描述了一种高通量版晕圈试验的方案,该方案使用一个由384个针组成的阵列,将约200纳升的储备溶液从化合物板转移到接种酵母的单孔板上。使用酶标仪的吸光度模式,可以对产生的晕圈进行定量,并将数据以平面文件的形式存档,这些文件可以通过标准软件连接到化合物数据库。该试验具有传统晕圈试验视觉读数的便利性,但使用的材料要少得多,并且可以自动化,每天筛选数千种化合物。