Djordjevic Marko, Sengupta Anirvan M
Department of Physics, Columbia University, New York, NY 10027, USA.
Phys Biol. 2005 Dec 16;3(1):13-28. doi: 10.1088/1478-3975/3/1/002.
SELEX (systematic evolution of ligands by exponential enrichment) is an experimental procedure that allows the extraction, from an initially random pool of DNA, of those oligomers with high affinity for a given DNA-binding protein. We address what is a suitable experimental and computational procedure to infer parameters of transcription factor-DNA interaction from SELEX experiments. To answer this, we use a biophysical model of transcription factor-DNA interactions to quantitatively model SELEX. We show that a standard procedure is unsuitable for obtaining accurate interaction parameters. However, we theoretically show that a modified experiment in which chemical potential is fixed through different rounds of the experiment allows robust generation of an appropriate dataset. Based on our quantitative model, we propose a novel bioinformatic method of data analysis for such a modified experiment and apply it to extract the interaction parameters for a mammalian transcription factor CTF/NFI. From a practical point of view, our method results in a significantly improved false positive/false negative trade-off, as compared to both the standard information theory based method and a widely used empirically formulated procedure.
SELEX(指数富集配体系统进化)是一种实验方法,可从最初随机的DNA文库中筛选出对特定DNA结合蛋白具有高亲和力的寡聚体。我们探讨了从SELEX实验推断转录因子与DNA相互作用参数的合适实验和计算方法。为了回答这个问题,我们使用转录因子与DNA相互作用的生物物理模型对SELEX进行定量建模。我们表明,标准方法不适用于获得准确的相互作用参数。然而,我们从理论上证明,通过在不同轮次实验中固定化学势的改进实验能够可靠地生成合适的数据集。基于我们的定量模型,我们为这种改进实验提出了一种新颖的生物信息学数据分析方法,并将其应用于提取哺乳动物转录因子CTF/NFI的相互作用参数。从实际角度来看,与基于标准信息论的方法和广泛使用的经验公式化方法相比,我们的方法在假阳性/假阴性权衡方面有显著改进。