Center for Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA 02139, USA.
Biomaterials. 2011 Jan;32(3):841-8. doi: 10.1016/j.biomaterials.2010.09.026. Epub 2010 Oct 20.
The emergence of combinatorial chemistries and the increased discovery of natural compounds have led to the production of expansive libraries of drug candidates and vast numbers of compounds with potentially interesting biological activities. Despite broad interest in high throughput screening (HTS) across varied fields of biological research, there has not been an increase in accessible HTS technologies. Here, we present a simple microarray sandwich system suitable for screening chemical libraries in cell-based assays at the benchtop. The microarray platform delivers chemical compounds to isolated cell cultures by 'sandwiching' chemical-laden arrayed posts with cell-seeded microwells. In this way, an array of sealed cell-based assays was generated without cross-contamination between neighbouring assays. After chemical exposure, cell viability was analyzed by fluorescence detection of cell viability assays on a per microwell basis using a standard microarray scanner. We demonstrate the efficacy of the system by generating four hits from toxicology screens towards MCF-7 human breast cancer cells. Three of the hits were identified in a combinatorial screen of a library of natural compounds in combination with verapamil, a P-glycoprotein inhibitor. A fourth hit, 9-methoxy-camptothecin, was identified by screening the natural compound library in the absence of verapamil. The method developed here miniaturizes existing HTS systems and enables the screening of a wide array of individual or combinatorial libraries in a reproducible and scalable manner. We anticipate broad application of such a system as it is amenable to combinatorial drug screening in a simple, robust and portable platform.
组合化学的出现和天然化合物的不断发现,导致了候选药物库的广泛扩展和具有潜在有趣生物活性的化合物数量的大量增加。尽管在生物研究的各个领域都广泛关注高通量筛选(HTS),但可获得的 HTS 技术并没有增加。在这里,我们提出了一种简单的微阵列三明治系统,适用于在台式机上进行基于细胞的测定中筛选化学文库。该微阵列平台通过用载有化学物质的排列柱“夹”住细胞接种的微孔来将化学物质递送到分离的细胞培养物中。通过这种方式,在没有相邻测定之间交叉污染的情况下,生成了一系列密封的基于细胞的测定。在化学暴露后,通过使用标准微阵列扫描仪逐个微孔荧光检测细胞活力测定来分析细胞活力。我们通过从 MCF-7 人乳腺癌细胞的毒理学筛选中生成四个命中物来证明该系统的功效。其中三个命中物是在天然化合物文库与维拉帕米(一种 P-糖蛋白抑制剂)的组合组合筛选中确定的。第四个命中物 9-甲氧基喜树碱是通过在没有维拉帕米的情况下筛选天然化合物文库而确定的。这里开发的方法使现有的 HTS 系统微型化,并能够以可重复和可扩展的方式筛选广泛的单个或组合文库。我们预计,由于该系统适用于在简单、稳健和便携式平台上进行组合药物筛选,因此将广泛应用于此类系统。