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通过胰岛素受体磷酸化定量对基于细胞的胰岛素受体调节剂筛选进行验证。

Validation of a cell-based screen for insulin receptor modulators by quantification of insulin receptor phosphorylation.

作者信息

Minor Lisa K, Westover Lori, Kong Yan, Patel Darpana, Wildey Mary Jo, Conway Bruce R, Demarest Keith T

机构信息

Johnson & Johnson Pharmaceutical Research and Development, L L C, Spring House, PA 19477, USA.

出版信息

J Biomol Screen. 2003 Aug;8(4):439-46. doi: 10.1177/1087057103255280.

Abstract

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.

摘要

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。

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