首页> 美国卫生研究院文献>Journal of Biomolecular Techniques : JBT >P92-M The ABI 3730 DNA Analyzer is an Efficient System for Simultaneous Bi-Directional Analysis of Dual-Labeled Probes Used to Study Protein-DNA Interactions
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P92-M The ABI 3730 DNA Analyzer is an Efficient System for Simultaneous Bi-Directional Analysis of Dual-Labeled Probes Used to Study Protein-DNA Interactions

机译:P92-M ABI 3730 DNA分析仪是一种高效的系统用于双向双向分析用于研究蛋白质-DNA相互作用的双标签探针

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摘要

DNA footprinting is a powerful tool to study regions of DNA where proteins bind. Traditionally, target DNA fragments are labeled with 32P, incubated with the protein of interest, then subjected to chemical nuclease attack. The DNA probe is then purified and nicked fragments analyzed on sequencing gels to reveal regions of DNA protected by the protein from attack.The traditional method is a time-consuming and difficult protocol requiring specialized skill. Proteins with low dissociation constants require an additional preparatory separation before analysis, which reduces the yield of bound probe. The isotope is labile, involves safety considerations, and requires a separate labeling and purification step. The finished gels must be dried down and exposed. This adds time to the overall process, varies according to the potency of the isotope, and decreases resolution. Normalization and alignment of free and bound probes is difficult. The one-dimensional nature of the single label necessitates separate analysis of each DNA strand, and the analytical gel limits the length of the analytical window.We have developed a novel method of DNA footprinting that utilizes the multi-dimensional nature of fluorophores to label both strands of the DNA target, which permits differential analysis of both strands simultaneously. Labeled primers are commercially available for use as PCR primers, permitting simultaneous labeling and amplification of the DNA probe. The use of the chemical nuclease 1,10-phenathroline-copper facilitates in-gel attack of free and bound probe, which increases the yield of bound probe and reduces perturbation of the three-dimensional conformation of the complex. Samples can be analyzed rapidly by standard automated sequencing instrumentation with baseline, base pair resolution. Software data manipulation reduces normalization issues. The result is high-quality data acquisition in a matter of hours instead of days.
机译:DNA足迹是研究蛋白质结合的DNA区域的强大工具。传统上,目标DNA片段用 32 P标记,与目标蛋白质一起孵育,然后进行化学核酸酶攻击。然后纯化DNA探针,并在测序凝胶上分析带缺口的片段,以揭示受蛋白质保护的DNA区域免受攻击。传统方法是一项耗时且困难的操作,需要专门技能。具有低解离常数的蛋白质在分析之前需要进行额外的准备分离,这会降低结合探针的产量。同位素不稳定,涉及安全考虑,并且需要单独的标记和纯化步骤。成品凝胶必须干燥并暴露。这增加了整个过程的时间,根据同位素的效力而变化,并降低了分离度。游离和结合探针的标准化和比对是困难的。单标记的一维性质需要对每条DNA链进行单独分析,并且分析凝胶限制了分析窗口的长度。 DNA靶标的双链,可同时进行两条链的差异分析。标记的引物可商购获得,用作PCR引物,可同时标记和扩增DNA探针。化学核酸酶1,10-菲咯啉-铜的使用促进了游离和结合探针的凝胶内攻击,这增加了结合探针的产率并减少了复合物三维构象的干扰。可以使用具有基线,碱基对分辨率的标准自动测序仪器对样品进行快速分析。软件数据处理减少了标准化问题。结果是数小时而不是数天的高质量数据采集。

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