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均相时间分辨荧光及其在药物研发中激酶分析的应用。

Homogeneous time-resolved fluorescence and its applications for kinase assays in drug discovery.

作者信息

Jia Yong, Quinn Christopher M, Gagnon Andrew I, Talanian Robert

机构信息

Department of Molecular Pharmacology, Abbott Bioresearch Center, Worcester, MA 01605, USA.

出版信息

Anal Biochem. 2006 Sep 15;356(2):273-81. doi: 10.1016/j.ab.2006.05.006. Epub 2006 May 24.

Abstract

The rapidly growing interest in kinases as potential targets for therapeutic intervention has prompted the development of many kinase assay technologies. One exciting example is homogeneous time-resolved fluorescence (HTRF). An HTRF assay utilizes the signal generated by the fluorescence resonance energy transfer between donor and acceptor molecules in close proximity. Dual-wavelength detection helps to eliminate media interference, and the final signal is proportional to the extent of product formation. Thus far, the reported applications of this technology for in vitro kinase assays have mainly focused on high-throughput screening. In this report, we extend the applications of HTRF technology to the areas of enzyme and inhibitor characterization, some aspects of which were previously believed impossible. We describe the methods developed for determining the kinetic parameters of an enzyme, such as K(m) and k(cat), and the procedures for inhibitor mechanistic studies including ATP competitiveness and slow-binding and dissociation kinetics. These assays can be readily applied to any kinase and are valuable in advancing a program through the early stages of drug discovery.

摘要

激酶作为治疗干预潜在靶点的兴趣迅速增长,促使了许多激酶检测技术的发展。一个令人兴奋的例子是均相时间分辨荧光(HTRF)。HTRF检测利用供体和受体分子之间紧密接近时荧光共振能量转移产生的信号。双波长检测有助于消除介质干扰,最终信号与产物形成的程度成正比。到目前为止,该技术在体外激酶检测中的报道应用主要集中在高通量筛选上。在本报告中,我们将HTRF技术的应用扩展到酶和抑制剂表征领域,其中一些方面以前被认为是不可能的。我们描述了用于确定酶动力学参数(如K(m)和k(cat))的方法,以及抑制剂机制研究的程序,包括ATP竞争性、慢结合和解离动力学。这些检测方法可轻松应用于任何激酶,在药物发现的早期阶段推进项目方面具有重要价值。

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