Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA.
Department of Chemistry, New York University, New York, NY 10003, USA.
Science. 2015 Feb 20;347(6224):1260901. doi: 10.1126/science.1260901.
For over half a century, the biological roles of nucleic acids as catalytic enzymes, intracellular regulatory molecules, and the carriers of genetic information have been studied extensively. More recently, the sequence-specific binding properties of DNA have been exploited to direct the assembly of materials at the nanoscale. Integral to any methodology focused on assembling matter from smaller pieces is the idea that final structures have well-defined spacings, orientations, and stereo-relationships. This requirement can be met by using DNA-based constructs that present oriented nanoscale bonding elements from rigid core units. Here, we draw analogy between such building blocks and the familiar chemical concepts of "bonds" and "valency" and review two distinct but related strategies that have used this design principle in constructing new configurations of matter.
半个多世纪以来,核酸作为催化酶、细胞内调节分子以及遗传信息载体的生物学作用得到了广泛研究。最近,人们利用 DNA 的序列特异性结合特性来指导纳米尺度材料的组装。任何一种专注于将物质从小型部件组装起来的方法的关键是,最终结构具有明确的间距、取向和立体关系。通过使用基于 DNA 的构建体,可以满足这一要求,这些构建体从刚性核心单元呈现定向纳米级键合元素。在这里,我们将这些构建块与熟悉的化学概念“键”和“价”进行类比,并回顾两种不同但相关的策略,它们使用这一设计原则构建了物质的新构型。