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利用发光技术开发激酶检测方法:以细胞周期蛋白依赖性激酶4作为模型系统。

Utilization of luminescent technology to develop a kinase assay: Cdk4 as a model system.

作者信息

Tagliati Federico, Bottoni Arianna, Bosetti Alessandro, Zatelli Maria Chiara, degli Uberti Ettore C

机构信息

Section of Endocrinology, Department of Biomedical Sciences and Advanced Therapies, University of Ferrara, Via Savonarola 9, 44100 Ferrara, Italy.

出版信息

J Pharm Biomed Anal. 2005 Sep 15;39(3-4):811-4. doi: 10.1016/j.jpba.2005.05.003.

Abstract

Protocols to assess kinase activity generally include radioactive methods, fluorescent polarization technology and the use of specific antibodies. Here, a simple, effective, non radioactive method to measure kinase activity of immunoprecipitated proteins is described. Cdk4, a cell cycle dependent enzyme, was immunoprecipitated from whole cell extracts and used in kinase reactions. This system has been developed taking advantage of the kinase-Glo reagent (Promega), based on ATP depletion technology, but with a wider range of applications. The original aim of the commercial kit is the evaluation of kinase activity of highly purified enzymes, while this system enabled the evaluation of native kinases, retrieved by immunoprecipitation. This method was highly homogeneous and did not require any kind of separation or purification as well. Moreover, it was suitable for basic research and may be useful for low-medium throughput pharmaceutical screening of chemical libraries.

摘要

评估激酶活性的方法通常包括放射性方法、荧光偏振技术以及使用特异性抗体。在此,我们描述了一种简单、有效、非放射性的方法来测量免疫沉淀蛋白的激酶活性。细胞周期依赖性酶Cdk4从全细胞提取物中免疫沉淀出来,并用于激酶反应。该系统利用基于ATP消耗技术的Kinase-Glo试剂(普洛麦格公司)开发而成,但具有更广泛的应用范围。该商业试剂盒的最初目的是评估高度纯化酶的激酶活性,而此系统能够评估通过免疫沉淀回收的天然激酶。该方法具有高度均一性,也无需任何种类的分离或纯化。此外,它适用于基础研究,可能对化学文库的低中通量药物筛选有用。

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