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用于TRAF6泛素聚合的高通量时间分辨荧光共振能量转移检测方法的开发。

Development of a high throughput time-resolved fluorescence resonance energy transfer assay for TRAF6 ubiquitin polymerization.

作者信息

Hong Catherine A, Swearingen Elissa, Mallari Rommel, Gao Xiong, Cao Zhaodan, North Anne, Young Stephen W, Huang Shu-Gui

机构信息

Tularik Inc., South San Francisco, CA, USA.

出版信息

Assay Drug Dev Technol. 2003 Feb;1(1 Pt 2):175-80. doi: 10.1089/154065803321537890.

Abstract

Interleukin 1 receptor activation innervates a cascade of signal transduction events that ultimately lead to the activation of inflammatory and immune response genes. TRAF6 is a Ub ligase (E3) involved in this pathway, and inhibition of this critical enzyme may provide a means for treating inflammatory and immune diseases. A TR-FRET assay has been developed and evaluated for HTS for TRAF6 inhibitors. Bio-Ub and Eu-Ub were polymerized in the presence of Ub activating enzyme E1, conjugating enzyme E2, and TRAF6. Following a 2-h incubation, the reaction was stopped with a buffer containing 10 m M EDTA and the fluorescence donor SA-APC. Fluorescence energy transfer from Eu to APC was measured as a ratio of fluorescence intensity at 655 nm to that at 615 nm (excitation at 340 nm). This homogeneous assay has been optimized and validated in a 384-well format. A window of five- to eightfold and Z' factor of 0.6-0.8 suggests that this assay can be applied to screen for inhibitors of the polyubiquitination activity of TRAF6.

摘要

白细胞介素1受体激活引发一系列信号转导事件,最终导致炎症和免疫反应基因的激活。TRAF6是参与该途径的一种泛素连接酶(E3),抑制这种关键酶可能为治疗炎症和免疫疾病提供一种方法。已开发并评估了一种用于高通量筛选TRAF6抑制剂的时间分辨荧光共振能量转移(TR-FRET)检测方法。在泛素激活酶E1、结合酶E2和TRAF6存在的情况下,将生物素化泛素(Bio-Ub)和铕标记泛素(Eu-Ub)聚合。孵育2小时后,用含有10 mM EDTA和荧光供体链霉亲和素-别藻蓝蛋白(SA-APC)的缓冲液终止反应。测量从铕到别藻蓝蛋白的荧光能量转移,以655 nm处的荧光强度与615 nm处的荧光强度之比表示(激发波长为340 nm)。这种均相检测方法已在384孔板形式中进行了优化和验证。五到八倍的窗口值和0.6 - 0.8的Z'因子表明该检测方法可用于筛选TRAF6多聚泛素化活性的抑制剂。

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