Confer Health, Inc., Charlestown, MA 02143, USA.
Biological Sciences, Institute for Life Sciences, University of Southampton, Southampton, Hampshire SO17 1BJ, UK.
Nucleic Acids Res. 2018 Feb 16;46(3):1021-1037. doi: 10.1093/nar/gkx1230.
DNA self-assembly has proved to be a useful bottom-up strategy for the construction of user-defined nanoscale objects, lattices and devices. The design of these structures has largely relied on exploiting simple base pairing rules and the formation of double-helical domains as secondary structural elements. However, other helical forms involving specific non-canonical base-base interactions have introduced a novel paradigm into the process of engineering with DNA. The most notable of these is a three-stranded complex generated by the binding of a third strand within the duplex major groove, generating a triple-helical ('triplex') structure. The sequence, structural and assembly requirements that differentiate triplexes from their duplex counterparts has allowed the design of nanostructures for both dynamic and/or structural purposes, as well as a means to target non-nucleic acid components to precise locations within a nanostructure scaffold. Here, we review the properties of triplexes that have proved useful in the engineering of DNA nanostructures, with an emphasis on applications that hitherto have not been possible by duplex formation alone.
DNA 自组装已被证明是构建用户定义的纳米级物体、晶格和器件的一种有用的自下而上的策略。这些结构的设计在很大程度上依赖于利用简单的碱基配对规则和形成双螺旋结构作为二级结构元件。然而,其他涉及特定非经典碱基-碱基相互作用的螺旋形式为 DNA 工程过程引入了一个新的范例。其中最引人注目的是由双链大沟内第三条链结合产生的三链复合物,生成三螺旋(“三聚体”)结构。区分三聚体与其双链对应物的序列、结构和组装要求,允许设计用于动态和/或结构目的的纳米结构,以及将非核酸成分靶向到纳米结构支架内精确位置的手段。在这里,我们回顾了在 DNA 纳米结构工程中被证明有用的三聚体的性质,重点介绍了仅通过双链形成不可能实现的应用。