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评估HTRF转录因子ADP检测技术的效用:与标准HTRF检测技术的比较。

Evaluating the utility of the HTRF Transcreener ADP assay technology: a comparison with the standard HTRF assay technology.

作者信息

Hong Lin, Quinn Christopher M, Jia Yong

机构信息

Department of Kinase Biology/Oncology, Genomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.

出版信息

Anal Biochem. 2009 Aug 1;391(1):31-8. doi: 10.1016/j.ab.2009.04.033. Epub 2009 May 3.

Abstract

The HTRF (homogeneous time-resolved fluorescence) Transcreener ADP assay is a new kinase assay technology marketed by Cis-Bio International (Bagnols-Cèze, France). It measures kinase activity by detecting the formation of ADP using a monoclonal antibody and HTRF detection principles. In this article, we compare this technology with a standard HTRF kinase assay using EGFR [L858R/T790M] mutant enzyme as a case study. We demonstrate that the HTRF Transcreener ADP assay generated similar kinetic constants and inhibitor potency compared with the standard HTRF assay. However, the smaller dynamic window and lower Z' factor of the HTRF Transcreener ADP assay make this format less preferable for high-throughput screening. Based on the assay principle, the HTRF Transcreener ADP assay can detect both kinase and ATPase activities simultaneously. The ability to probe ATPase activity opens up new avenues for assaying kinases with intrinsic ATPase activity without the need to identify substrates, and this can speed up the drug discovery process. However, caution must be exercised because any contaminating ATPase activity will result in an invalid assay. The inability to tolerate high concentrations of ATP in the assay will also limit the application of this technology, especially in compound mechanistic studies such as ATP competition. Overall, the HTRF Transcreener ADP assay provides a new alternative tool to complement existing assay technologies for drug discovery.

摘要

HTRF(均相时间分辨荧光)ADP检测法是由Cis-Bio International公司(法国巴尼奥勒-塞兹)推出的一种新型激酶检测技术。它利用单克隆抗体和HTRF检测原理,通过检测ADP的形成来测定激酶活性。在本文中,我们以EGFR [L858R/T790M] 突变酶为例,将该技术与标准的HTRF激酶检测法进行了比较。我们证明,与标准HTRF检测法相比,HTRF ADP检测法产生了相似的动力学常数和抑制剂效力。然而,HTRF ADP检测法较小的动态范围和较低的Z'因子使其不太适合用于高通量筛选。基于检测原理,HTRF ADP检测法可同时检测激酶和ATP酶活性。检测ATP酶活性的能力为检测具有内在ATP酶活性的激酶开辟了新途径,无需鉴定底物,这可以加快药物发现进程。然而,必须谨慎操作,因为任何污染性的ATP酶活性都会导致检测无效。该检测法无法耐受高浓度的ATP也会限制这项技术的应用,尤其是在诸如ATP竞争等化合物机制研究中。总体而言,HTRF ADP检测法提供了一种新的替代工具,以补充现有的药物发现检测技术。

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