Maculins Timurs, Carter Nikki, Dorval Thierry, Hudson Kevin, Nissink J Willem M, Hay Ronald T, Alwan Husam
Discovery Sciences, AstraZeneca, Alderley Park, Cheshire, SK10 4TG, UK.
Discovery Sciences, AstraZeneca, Darwin Building, Cambridge Science Park, Milton Road, Cambridge, CB4 0WG, UK.
Sci Rep. 2016 Jan 8;6:18940. doi: 10.1038/srep18940.
Ubiquitin signalling regulates most aspects of cellular life, thus deregulation of ubiquitylation has been linked with a number of diseases. E3 ubiquitin ligases provide substrate selectivity in ubiquitylation cascades and are therefore considered to be attractive targets for developing therapeutic molecules. In contrast to established drug target classes, such as protein kinases, GPCRs, hormone receptors and ion channels, ubiquitin drug discovery is in its early stages. This is, in part, due to the complexity of the ubiquitylation pathways and the lack of robust quantitative technologies that allow high-throughput screening of inhibitors. Here we report the development of a Ubiquitin Ligase Profiling system, which is a novel and generic cellular technology designed to facilitate identification of selective inhibitors against RING type E3 ubiquitin ligases. Utilization of this system requires a single co-transfection of cells with assay vectors, thereby enabling readout of E3 ubiquitin ligase catalytic activity within the cellular environment. Therefore, our robust high-throughput screening platform offers novel opportunities for the development of inhibitors against this difficult-to-target E3 ligase enzyme class.
泛素信号传导调节细胞生命的大多数方面,因此泛素化失调与多种疾病有关。E3泛素连接酶在泛素化级联反应中提供底物选择性,因此被认为是开发治疗分子的有吸引力的靶点。与已确立的药物靶点类别(如蛋白激酶、G蛋白偶联受体、激素受体和离子通道)相比,泛素药物发现尚处于早期阶段。部分原因在于泛素化途径的复杂性以及缺乏能够进行抑制剂高通量筛选的强大定量技术。在此,我们报告了泛素连接酶分析系统的开发,这是一种新型通用细胞技术,旨在促进针对RING型E3泛素连接酶的选择性抑制剂的鉴定。利用该系统需要将细胞与检测载体进行单次共转染,从而能够在细胞环境中读出E3泛素连接酶的催化活性。因此,我们强大的高通量筛选平台为开发针对这类难以靶向的E3连接酶的抑制剂提供了新机会。