用AlphaLISA在HTP模式下测定nf -κB p50与β-IFN-κB结合寡核苷酸的相互作用

Muniasamy Neerathilingam, S. H. A. Gandham, Falguni V Patel, M. Nasiruddin
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引用次数: 0

摘要

NF-κB在调节多种生物过程中发挥重要作用,包括先天免疫和适应性免疫、炎症、应激反应、b细胞发育和淋巴样器官发生。目前,广泛采用电泳迁移量转移法(EMSA)、酶联免疫吸附法(ELISA)、荧光共振能量转移法(FRET)和时间分辨荧光共振能量转移法(TR-FRET)等方法研究nf -κB与β-IFN-κB结合寡核苷酸的相互作用。这些技术中的每一种都具有不同的优点和缺点。我们描述了一种AlphaLISA方法来鉴定NFκB p50蛋白和β-IFN-κB结合寡核苷酸序列,并且在给定浓度(10 nM)下,在EMSA和Biacore的SPR检测中,相互作用是有效的。该方法具有体积小、通量高、样品制备和数据分析方便等优点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of Interaction between NFκB p50 and β-IFN-κB Binding Oligo Using AlphaLISA in HTP Fashion
NF-κB plays a crucial role in regulating various biological processes including innate and adaptive immunity, inflammation, stress responses, B-cell development, and lymphoid organogenesis. Currently, several assays like electrophoretic mobility shift assay (EMSA), enzyme-linked immunosorbent assay (ELISA), fluorescence resonance energy transfer (FRET) and time-resolved fluorescence resonance energy transfer (TR-FRET) are widely used for studying the NFκB intraction with β-IFN-κB binding oligo. Each of these techniques has varying utility with distinct strengths and weaknesses. We describe a method AlphaLISA to identify NFκB p50 protein and β-IFN-κB binding oligo sequence and interaction is efficient at a given concentration (10 nM) in the EMSA and Biacore’s SPR assays. The method has many advantages such as use of small volume, high throughput (HTP), convenience of sample preparation and data analysis.
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