Mondal Manas, Choudhury Devapriya, Chakrabarti Jaydeb, Bhattacharyya Dhananjay
Computational Science Division, Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata, 700064, India.
J Comput Aided Mol Des. 2015 Mar;29(3):283-95. doi: 10.1007/s10822-014-9828-x. Epub 2015 Jan 10.
Gene expression generally initiates from recognition of TATA-box binding protein (TBP) to the minor groove of DNA of TATA box sequence where the DNA structure is significantly different from B-DNA. We have carried out molecular dynamics simulation studies of TBP-DNA system to understand how the DNA structure alters for efficient binding. We observed rigid nature of the protein while the DNA of TATA box sequence has an inherent flexibility in terms of bending and minor groove widening. The bending analysis of the free DNA and the TBP bound DNA systems indicate presence of some similar structures. Principal coordinate ordination analysis also indicates some structural features of the protein bound and free DNA are similar. Thus we suggest that the DNA of TATA box sequence regularly oscillates between several alternate structures and the one suitable for TBP binding is induced further by the protein for proper complex formation.
基因表达通常始于TATA框结合蛋白(TBP)识别TATA框序列DNA的小沟,该DNA结构与B-DNA有显著差异。我们对TBP-DNA系统进行了分子动力学模拟研究,以了解DNA结构如何改变以实现有效结合。我们观察到蛋白质具有刚性,而TATA框序列的DNA在弯曲和小沟变宽方面具有固有的灵活性。游离DNA和TBP结合DNA系统的弯曲分析表明存在一些相似结构。主坐标分析也表明蛋白质结合的DNA和游离DNA的一些结构特征相似。因此,我们认为TATA框序列的DNA在几种交替结构之间有规律地振荡,蛋白质进一步诱导出适合TBP结合的结构以形成适当的复合物。