Gromiha M Michael
Computational Biology Research Center (CBRC), National Institute of Advanced Industrial Science and Technology (AIST), 2-42 Aomi, Koto-ku, Tokyo 135-0064, Japan.
J Biotechnol. 2005 May 4;117(2):137-45. doi: 10.1016/j.jbiotec.2004.12.016.
Protein-DNA recognition plays an essential role in the regulation of gene expression. The protein-DNA binding specificity is based on direct atomic contacts between protein and DNA and/or the conformational properties of DNA. In this work, we have analyzed the influence of DNA stiffness (E) to the specificity of protein-DNA complexes. The average DNA stiffness parameters for several protein-DNA complexes have been computed using the structure based sequence dependent stiffness scale. The relationship between DNA stiffness and experimental protein-DNA binding specificity has been brought out. We have investigated the importance of DNA stiffness with the aid of experimental free energy changes (DeltaDeltaG) due to binding in several protein-DNA complexes, such as, ETS proteins, 434, lambda, Mnt and trp repressors, 434 cro protein, EcoRV endonuclease V and zinc fingers. We found a correlation in the range 0.65-0.97 between DeltaDeltaG and E in these examples. Further, we have qualitatively analyzed the effect of mutations in the target sequence of lambda repressor and we observed that the DNA stiffness could correctly identify 70% of the correct bases among the considered nine positions.
蛋白质与DNA的识别在基因表达调控中起着至关重要的作用。蛋白质与DNA的结合特异性基于蛋白质与DNA之间的直接原子接触和/或DNA的构象性质。在这项工作中,我们分析了DNA刚性(E)对蛋白质-DNA复合物特异性的影响。使用基于结构的序列依赖性刚性标度计算了几种蛋白质-DNA复合物的平均DNA刚性参数。揭示了DNA刚性与实验性蛋白质-DNA结合特异性之间的关系。我们借助几种蛋白质-DNA复合物(如ETS蛋白、434、λ、Mnt和色氨酸阻遏物、434 cro蛋白、EcoRV核酸内切酶V和锌指)结合引起的实验自由能变化(ΔΔG),研究了DNA刚性的重要性。在这些例子中,我们发现ΔΔG与E之间的相关性在0.65 - 0.97范围内。此外,我们定性分析了λ阻遏物靶序列中突变的影响,并且观察到在考虑的九个位置中,DNA刚性能够正确识别70%的正确碱基。