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一种使用发光ADP积累技术的简单且强大的自动化激酶分析平台。

A Simple and robust automated kinase profiling platform using luminescent ADP accumulation technology.

作者信息

Larson Brad, Banks Peter, Zegzouti Hicham, Goueli Said A

机构信息

BioTek Instruments, Inc., Winooski, Vermont, USA.

出版信息

Assay Drug Dev Technol. 2009 Dec;7(6):573-84. doi: 10.1089/adt.2009.0216.

Abstract

Kinases continue to be one of the most important targets in today's drug discovery efforts. Following the identification of lead compounds through screening efforts, it is important to profile these leads against other kinases within that family, as well as from other families, to ascertain potential off-target effects. Because many kinase assays require the use of different substrates, optimization time and costs during profiling can be prohibitive. Here we demonstrate the versatility of a luminescent ADP accumulation assay, where one set of reagents can be used for a wide variety of kinases with differing K(m app) for ATP and substrates. Assay sensitivity allows for the use of low enzyme concentrations and small percent ATP conversion levels while still maintaining high signal:background ratios. We have used a simple, inexpensive automated pipetting system to automate the entire process from enzyme optimization through generation of compound IC(50) values. Agreement with literature values proves this combination of chemistry and instrumentation provides a simple, yet robust solution for automated kinase profiling.

摘要

激酶仍然是当今药物研发工作中最重要的靶点之一。通过筛选工作确定先导化合物后,针对该家族内以及其他家族的其他激酶对这些先导化合物进行分析,以确定潜在的脱靶效应,这一点很重要。由于许多激酶测定需要使用不同的底物,分析过程中的优化时间和成本可能过高。在此,我们展示了一种发光ADP积累测定法的多功能性,其中一组试剂可用于多种对ATP和底物具有不同表观米氏常数(K(m app))的激酶。该测定法的灵敏度允许使用低酶浓度和低ATP转化率水平,同时仍能保持高信号与背景比。我们使用了一种简单、廉价的自动移液系统,实现了从酶优化到生成化合物半数抑制浓度(IC(50))值的整个过程自动化。与文献值的一致性证明,这种化学方法与仪器的组合为自动激酶分析提供了一种简单而稳健的解决方案。

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