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使用全内反射荧光蛋白结合微阵列追踪DNA上的转录因子复合物

Tracking transcription factor complexes on DNA using total internal reflectance fluorescence protein binding microarrays.

作者信息

Bonham Andrew J, Neumann Thorsten, Tirrell Matthew, Reich Norbert O

机构信息

Department of Biomolecular Science & Engineering, University of California, Santa Barbara, CA, USA.

出版信息

Nucleic Acids Res. 2009 Jul;37(13):e94. doi: 10.1093/nar/gkp424. Epub 2009 May 31.

Abstract

We have developed a high-throughput protein binding microarray (PBM) assay to systematically investigate transcription regulatory protein complexes binding to DNA with varied specificity and affinity. Our approach is based on the novel coupling of total internal reflectance fluorescence (TIRF) spectroscopy, swellable hydrogel double-stranded DNA microarrays and dye-labeled regulatory proteins, making it possible to determine both equilibrium binding specificities and kinetic rates for multiple protein:DNA interactions in a single experiment. DNA specificities and affinities for the general transcription factors TBP, TFIIA and IIB determined by TIRF-PBM are similar to those determined by traditional methods, while simultaneous measurement of the factors in binary and ternary protein complexes reveals preferred binding combinations. TIRF-PBM provides a novel and extendible platform for multi-protein transcription factor investigation.

摘要

我们开发了一种高通量蛋白质结合微阵列(PBM)检测方法,以系统地研究与DNA具有不同特异性和亲和力的转录调节蛋白复合物。我们的方法基于全内反射荧光(TIRF)光谱、可膨胀水凝胶双链DNA微阵列和染料标记调节蛋白的新型耦合,使得在单个实验中能够确定多种蛋白质与DNA相互作用的平衡结合特异性和动力学速率。通过TIRF-PBM测定的通用转录因子TBP、TFIIA和IIB的DNA特异性和亲和力与传统方法测定的相似,而对二元和三元蛋白质复合物中这些因子的同时测量揭示了优选的结合组合。TIRF-PBM为多蛋白转录因子研究提供了一个新颖且可扩展的平台。

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