Li Wei, Yang Yang, Jiang Shuoxing, Yan Hao, Liu Yan
Department of Chemistry and Biochemistry, and Center for Molecular Design and Biomimicry, Biodesign Institute, Arizona State University , Tempe, Arizona 85287, United States.
J Am Chem Soc. 2014 Mar 12;136(10):3724-7. doi: 10.1021/ja411446q. Epub 2014 Mar 4.
Controlled nucleation of nanoscale building blocks by geometrically defined seeds implanted in DNA nanoscaffolds represents a unique strategy to study and understand the dynamic processes of molecular self-assembly. Here we utilize a two-dimensional DNA origami frame with a hollow interior and selectively positioned DNA hybridization seeds to control the self-assembly of DNA tile building blocks, where the small DNA tiles are directed to fill the interior of the frame through prescribed sticky end interactions. This design facilitates the construction of DNA origami/array hybrids that adopt the overall shape and dimensions of the origami frame, forming a 2D array in the core consisting of a large number of simple repeating DNA tiles. The formation of the origami/array hybrid was characterized with atomic force microscopy, and the nucleation dynamics were monitored by serial AFM scanning and fluorescence spectroscopy, which revealed faster kinetics of growth within the frame as compared to growth without the presence of a frame. Our study provides insight into the fundamental behavior of DNA-based self-assembling systems.
通过植入DNA纳米支架中的几何定义种子对纳米级构建块进行可控成核,是研究和理解分子自组装动态过程的独特策略。在这里,我们利用具有中空内部的二维DNA折纸框架和选择性定位的DNA杂交种子来控制DNA瓦片构建块的自组装,其中小的DNA瓦片通过规定的粘性末端相互作用被引导填充框架内部。这种设计有助于构建采用折纸框架整体形状和尺寸的DNA折纸/阵列杂交体,在核心区域形成由大量简单重复DNA瓦片组成的二维阵列。用原子力显微镜对折纸/阵列杂交体的形成进行了表征,通过连续原子力显微镜扫描和荧光光谱监测成核动力学,结果表明与没有框架存在时的生长相比,框架内的生长动力学更快。我们的研究为基于DNA的自组装系统的基本行为提供了见解。