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8臂和12臂DNA分支连接体的组装与表征

Assembly and characterization of 8-arm and 12-arm DNA branched junctions.

作者信息

Wang Xing, Seeman Nadrian C

机构信息

Contribution from the Department of Chemistry, New York University, New York, NY 10003, USA.

出版信息

J Am Chem Soc. 2007 Jul 4;129(26):8169-76. doi: 10.1021/ja0693441. Epub 2007 Jun 12.

Abstract

Branched DNA molecules can be assembled into objects and networks directed by sticky-ended cohesion. The connectivity of these species is limited by the number of arms flanking the branch point. To date, the only branched junctions constructed contain six or fewer arms. We report the construction of DNA branched junctions that contain either 8 or 12 double-helical arms surrounding a branch point. The design of the 8-arm junction exploits the limits of a previous approach to thwart branch migration, but the design of the 12-arm junction uses a new to principle achieve this end. The 8-arm junction is stable with 16 nucleotide pairs per arm, but the 12-arm junction has been stabilized by 24 nucleotide pairs per arm. Ferguson analysis of these junctions in combination with 3-, 4-, 5-, and 6-arm junctions indicates a linear increase in friction constant as the number of arms increases; the 4-arm junction migrates anomalously at 4 degrees C, suggesting stacking of its domains. All strands in both the 8-arm and 12-arm junctions show similar responses to hydroxyl radical autofootprinting analysis, indicating that they lack any dominant stacking structures. The stability of the 12-arm junction demonstrates that the number of arms in a junction is not limited to the case of having adjacent identical base pairs flanking the junction. The ability to construct 8-arm and 12-arm junctions increases the number of objects, graphs, and networks that can be built from branched DNA components. In principle, the stick structure corresponding to cubic close-packing is now a possible target for assembly by DNA nanotechnology.

摘要

分支DNA分子可以通过粘性末端凝聚作用组装成物体和网络。这些分子的连接性受到分支点两侧臂数量的限制。迄今为止,构建的唯一分支连接点包含六个或更少的臂。我们报告了一种DNA分支连接点的构建,该连接点在分支点周围包含8个或12个双螺旋臂。8臂连接点的设计利用了先前一种阻止分支迁移方法的局限性,但12臂连接点的设计采用了一种新原理来实现这一目的。8臂连接点每臂有16个核苷酸对时是稳定的,但12臂连接点每臂有24个核苷酸对时已实现稳定。对这些连接点与3臂、4臂、5臂和6臂连接点进行弗格森分析表明,随着臂数量的增加,摩擦常数呈线性增加;4臂连接点在4℃时迁移异常,表明其结构域存在堆积现象。8臂和12臂连接点中的所有链对羟基自由基自足迹分析都显示出相似的响应,表明它们缺乏任何占主导地位的堆积结构。12臂连接点的稳定性表明,连接点中的臂数量并不局限于连接点两侧有相邻相同碱基对的情况。构建8臂和12臂连接点的能力增加了可以由分支DNA组件构建的物体、图形和网络的数量。原则上,对应于立方密堆积的棒状结构现在成为DNA纳米技术组装的一个可能目标。

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