Eyckerman Sven, Lemmens Irma, Catteeuw Dominiek, Verhee Annick, Vandekerckhove Joel, Lievens Sam, Tavernier Jan
Flanders Interuniversity Institute for Biotechnology, VIB09, Department of Medical Protein Research, Faculty of Medicine and Health Sciences, Ghent University, A. Baertsoenkaai 3, B-9000 Ghent, Belgium.
Nat Methods. 2005 Jun;2(6):427-33. doi: 10.1038/nmeth760.
Interactions between proteins are at the heart of the cellular machinery. It is therefore not surprising that altered interaction profiles caused by aberrant protein expression patterns or by the presence of mutations can trigger cellular dysfunction, eventually leading to disease. Moreover, many viral and bacterial pathogens rely on protein-protein interactions to exert their damaging effects. Interfering with such interactions is an obvious pharmaceutical goal, but detailed insights into the protein binding properties as well as efficient screening platforms are needed. In this report, we describe a cytokine receptor-based assay with a positive readout to screen for disrupters of designated protein-protein interactions in intact mammalian cells and evaluate this concept using polypeptides as well as small organic molecules. These reverse mammalian protein-protein interaction trap (MAPPIT) screens were developed to monitor interactions between the erythropoietin receptor (EpoR) and suppressors of cytokine signaling (SOCS) proteins, between FKBP12 and ALK4, and between MDM2 and p53.
蛋白质之间的相互作用是细胞机制的核心。因此,由异常蛋白质表达模式或突变的存在引起的相互作用谱改变会引发细胞功能障碍,最终导致疾病,这并不奇怪。此外,许多病毒和细菌病原体依靠蛋白质-蛋白质相互作用来发挥其破坏作用。干扰此类相互作用是一个明确的药物研发目标,但需要对蛋白质结合特性有详细的了解以及高效的筛选平台。在本报告中,我们描述了一种基于细胞因子受体的检测方法,该方法具有阳性读数,用于筛选完整哺乳动物细胞中特定蛋白质-蛋白质相互作用的破坏剂,并使用多肽以及小分子来评估这一概念。这些反向哺乳动物蛋白质-蛋白质相互作用捕获(MAPPIT)筛选方法旨在监测促红细胞生成素受体(EpoR)与细胞因子信号转导抑制因子(SOCS)蛋白之间、FKBP12与ALK4之间以及MDM2与p53之间的相互作用。