Walker W L, Landaw E M, Dickerson R E, Goodsell D S
Department of Biomathematics and the Molecular Biology Institute, University of California, Los Angeles, CA 90024, USA.
Proc Natl Acad Sci U S A. 1997 May 27;94(11):5634-9. doi: 10.1073/pnas.94.11.5634.
Three- and four-ring polyamides containing N-methylimidazole and N-methylpyrrole, and their hairpin-linked derivatives, bind side-by-side in the minor groove of DNA in a sequence-specific manner. The sequences recognized by side-by-side molecules are dependent on the pairings of the polyamide rings to the bases. In this study we report a mathematical model for estimating the free energies of binding for gamma-aminobutyric acid-linked polyamides to 5- and 6-bp DNA sequences. The model parameters are calibrated by a least-squares fit to 35 experimental binding constants. The model performs well in cross-validation experiments and the parameters are consistent with previously proposed empirical rules of polyamide-DNA binding. We apply the model to the design of targeted polyamides, evaluating the ability of the proposed polyamides to bind to a DNA sequence of interest while minimizing binding to the remaining DNA sequences.
含有N-甲基咪唑和N-甲基吡咯的三环和四环聚酰胺及其发夹连接衍生物,以序列特异性方式在DNA小沟中并排结合。并排分子识别的序列取决于聚酰胺环与碱基的配对。在本研究中,我们报告了一个数学模型,用于估计γ-氨基丁酸连接的聚酰胺与5和6个碱基对的DNA序列结合的自由能。通过对35个实验结合常数进行最小二乘拟合来校准模型参数。该模型在交叉验证实验中表现良好,且参数与先前提出的聚酰胺-DNA结合的经验规则一致。我们将该模型应用于靶向聚酰胺的设计,评估所提出的聚酰胺与感兴趣的DNA序列结合的能力,同时尽量减少与其余DNA序列的结合。