Development of a HTRF kinase assay for determination of Syk activity.

Christopher Harbert, Jeannette Marshall, Sharon Soh, Krista Steger
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引用次数: 13

Abstract

Regulation of protein phosphorylation is a primary cellular signaling mechanism. Many cellular responses to internal and external events are mitigated by protein kinase signaling cascades. Dysfunction of protein kinase activity has been linked to a variety of human pathologies, in the areas of cancer, inflammation, metabolism, cell cycle, apoptosis, as well as cardiovascular, neurodegenerative and autoimmune diseases. As such, there is an important need for protein kinase activity detection methodologies for researchers engaged in Drug Discovery. A number of different technologies have been employed for the measurement of protein kinase activity, including radioactive methods, luminescent methods, and fluorescent methods. More recently, Homogeneous Time Resolved Fluorescence technology (HTRF), based on the principle of time-resolved fluorescent resonance energy transfer (TR-FRET), has been developed and applied for the measurement of protein kinase activity in vitro. This technology note describes the development of an HTRF assay for detection of Syk enzyme activity in a format consistent with the requirements of High-Throughput Screening (HTS) campaigns currently used in drug discovery.

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HTRF激酶Syk活性测定方法的建立。
蛋白磷酸化调控是细胞主要的信号传导机制。许多细胞对内部和外部事件的反应是通过蛋白激酶信号级联反应来减轻的。蛋白激酶活性的功能障碍与多种人类病理有关,包括癌症、炎症、代谢、细胞周期、细胞凋亡以及心血管、神经退行性和自身免疫性疾病。因此,对于从事药物发现的研究人员来说,蛋白激酶活性检测方法是一个重要的需求。许多不同的技术已被用于测量蛋白激酶活性,包括放射性方法,发光方法和荧光方法。最近,基于时间分辨荧光共振能量转移(TR-FRET)原理的均匀时间分辨荧光技术(HTRF)已被开发并应用于体外蛋白激酶活性的测量。本技术说明描述了一种用于Syk酶活性检测的HTRF试验的开发,其格式与目前用于药物发现的高通量筛选(HTS)活动的要求一致。
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