Harbert Christopher, Marshall Jeannette, Soh Sharon, Steger Krista
Cisbio US Inc., 12 Deangelo Dr., Bedford MA 01730, USA.
Curr Chem Genomics. 2008 Feb 25;1:20-6. doi: 10.2174/1875397300801010020.
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.
蛋白质磷酸化的调节是一种主要的细胞信号传导机制。细胞对内部和外部事件的许多反应通过蛋白激酶信号级联反应得到缓解。蛋白激酶活性的功能障碍与癌症、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等多种人类疾病相关。因此,从事药物发现的研究人员迫切需要蛋白质激酶活性检测方法。已经采用了许多不同的技术来测量蛋白激酶活性,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)原理的均相时间分辨荧光技术(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HTRF测定法的开发,该测定法用于检测Syk酶活性,其形式符合药物发现中当前使用的高通量筛选(HTS)活动的要求。