Paukstelis Paul J, Nowakowski Jacek, Birktoft Jens J, Seeman Nadrian C
Institute for Cellular and Molecular Biology, University of Texas at Austin, 1 University Station A4800, Austin, Texas 78712, USA.
Chem Biol. 2004 Aug;11(8):1119-26. doi: 10.1016/j.chembiol.2004.05.021.
DNA has proved to be a versatile material for the rational design and assembly of nanometer scale objects. Here we report the crystal structure of a continuous three-dimensional DNA lattice formed by the self-assembly of a DNA 13-mer. The structure consists of stacked layers of parallel helices with adjacent layers linked through parallel-stranded base pairing. The hexagonal lattice geometry contains solvent channels that appear large enough to allow 3'-linked guest molecules into the crystal. We have successfully used these parallel base pairs to design and produce crystals with greatly enlarged solvent channels. This lattice may have applications as a molecular scaffold for structure determination of guest molecules, as a molecular sieve, or in the assembly of molecular electronics. Predictable non-Watson-Crick base pairs, like those described here, may present a new tool in structural DNA nanotechnology.
DNA已被证明是一种用于合理设计和组装纳米级物体的多功能材料。在此,我们报告了由一个DNA 13聚体自组装形成的连续三维DNA晶格的晶体结构。该结构由平行螺旋的堆叠层组成,相邻层通过平行链碱基配对相连。六边形晶格几何结构包含溶剂通道,这些通道看起来足够大,能够允许3'-连接的客体分子进入晶体。我们已成功利用这些平行碱基对设计并制备出具有大大扩大的溶剂通道的晶体。这种晶格可作为用于确定客体分子结构的分子支架、分子筛或用于分子电子学组装。像这里所描述的可预测的非沃森-克里克碱基对,可能会成为结构DNA纳米技术中的一种新工具。