Minor Lisa K, Westover Lori, Kong Yan, Patel Darpana, Wildey Mary Jo, Conway Bruce R, Demarest Keith T
Johnson & Johnson Pharmaceutical Research and Development, L L C, Spring House, PA 19477, USA.
J Biomol Screen. 2003 Aug;8(4):439-46. doi: 10.1177/1087057103255280.
Stimulation of a cell with insulin initiates a signal transduction cascade that results in cellular activities that include phosphorylation of the receptor itself. Measurement of the degree of phosphorylation can serve as a marker for receptor activation. Receptor phosphorylation has been measured using Western blot analysis, which is very low throughput and not easily quantifiable. The goal of this project was to develop a cell-based assay to measure receptor phosphorylation in high throughput. This report describes a cell-based assay for insulin receptor phosphorylation that is robust and amenable to high-volume screening in a microwell format.
用胰岛素刺激细胞会启动一个信号转导级联反应,该反应会导致包括受体自身磷酸化在内的细胞活动。磷酸化程度的测量可作为受体激活的标志物。受体磷酸化已通过蛋白质印迹分析进行测量,这种方法通量非常低且不易定量。本项目的目标是开发一种基于细胞的检测方法,以高通量方式测量受体磷酸化。本报告描述了一种用于胰岛素受体磷酸化的基于细胞的检测方法,该方法稳健且适用于微孔板形式的大量筛选。