Antczak Christophe, Djaballah Hakim
HTS Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Center for Proteomic Chemistry, Novartis Institutes for Biomedical Research, 250 Massachusetts Avenue, Cambridge, MA, 02139, USA.
Methods Mol Biol. 2016;1360:97-106. doi: 10.1007/978-1-4939-3073-9_8.
Cell-based assays have the potential and advantage to identify cell-permeable modulators of kinase function, and hence provide an alternative to the conventional enzymatic activity-driven discovery approaches that rely on purified recombinant kinase catalytic domains. Here, we describe a domain-based high-content biosensor approach to study endogenous EGFR activity whereby EGF-induced receptor activation, subsequent trafficking, and internalization are imaged and quantified using time-dependent granule formation in cells. This method can readily be used to search for EGFR modulators in both chemical and RNAi screening; with potential applicability to other receptor tyrosine kinases.
基于细胞的检测方法有潜力和优势来鉴定激酶功能的细胞渗透性调节剂,从而为依赖纯化重组激酶催化结构域的传统酶活性驱动的发现方法提供一种替代方案。在此,我们描述了一种基于结构域的高内涵生物传感器方法来研究内源性表皮生长因子受体(EGFR)活性,通过利用细胞中随时间变化的颗粒形成对表皮生长因子(EGF)诱导的受体激活、随后的转运和内化进行成像和定量分析。该方法可轻松用于化学和RNA干扰筛选中寻找EGFR调节剂;可能适用于其他受体酪氨酸激酶。