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Toward a Designed Functioning Genetic System With Expanded-size Base Pairs: Solution Structure of the 8-Base xDNA Double Helix

机译:建立具有扩展碱基对的设计的功能遗传系统:8碱基xDNA双螺旋的溶液结构

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摘要

We describe the NMR-derived solution structure of the double helical form of a designed 8-base genetic pairing system, termed xDNA. The benzo-homologous xDNA design contains base pairs that are wider than natural DNA pairs by ca. 2.4 Å (the width of a benzene ring). The eight component bases of this xDNA helix are A, C, G, T, xA, xT, xC, and xG. The structure was solved in aqueous buffer using 1D and 2D NMR methods combined with restrained molecular dynamics. The data show that the decamer duplex is right-handed and antiparallel, and hydrogen-bonded in the analogous way as Watson-Crick DNA. The sugar-phosphate backbone adopts a regular conformation similar to that of B-form DNA, with small dihedral adjustments due to the larger circumference of the helix. The grooves are much wider and more shallow than those of B-form DNA, and the helix turn is slower, with ca. 12 base pairs per 360° turn. There is extensive intra- and inter-strand base stacking surface area, providing an explanation for the greater stability of xDNA relative to natural DNA. There is also evidence for greater motion in this structure compared to a previous two-base expanded helix; possible chemical and structural reasons for this are discussed. The results confirm paired self-assembly of the designed xDNA system. This suggests the possibility that other genetic system structures besides the natural one might be functional in encoding information and transferring it to new complementary strands.
机译:我们描述了被设计为基于xDNA的8碱基遗传配对系统的双螺旋形式的NMR衍生溶液结构。苯并同源的xDNA设计所包含的碱基对比天然DNA对的碱基约宽约20倍。 2.4Å(苯环的宽度)。该xDNA螺旋的八个组成部分是A,C,G,T,xA,xT,xC和xG。使用1D和2D NMR方法结合受限的分子动力学,在含水缓冲液中解析结构。数据显示,十聚体双链体是右旋且反平行的,并且以与Watson-Crick DNA类似的方式与氢键结合。糖磷酸主链采用类似于B型DNA的规则构象,由于螺旋的较大周长而具有较小的二面角调节。沟纹比B型DNA的沟纹更宽,更浅,螺旋转弯较慢,大约有。每360°转12个碱基对。广泛的链内和链间碱基堆积表面积,为xDNA相对于天然DNA的更大稳定性提供了解释。也有证据表明,与先前的两基扩展螺旋相比,该结构具有更大的运动;讨论了可能的化学和结构原因。结果证实了所设计的xDNA系统的配对自组装。这表明,除了自然遗传系统外,其他遗传系统结构也可能在编码信息并将其转移到新的互补链中发挥作用。

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