Department of Chemical and Biomolecular Engineering and ‡Division of Biomedical Engineering, The Hong Kong University of Science and Technology , Clear Water Bay, Kowloon, Hong Kong.
J Am Chem Soc. 2014 Jul 16;136(28):9810-3. doi: 10.1021/ja502904s. Epub 2014 Jun 30.
We present a nonlinear hybridization chain reaction (HCR) system in which a trigger DNA initiates self-sustained assembly of quenched double-stranded substrates into fluorescent dendritic nanostructures. During the process, an increasing number of originally sequestered trigger sequences labeled with fluorescent reporters are freed up from quenched substrates, leading to chain-branching growth of the assembled DNA dendrimers and an exponential increase in the fluorescence intensity. The triggered assembly behavior was examined by PAGE analysis, and the morphologies of the grown dendrimers were verified by AFM imaging. The exponential kinetics of the fluorescence accumulation was also confirmed by time-dependent fluorescence spectroscopy. This method adopts a simple sequence design strategy, the concept of which could be adapted to program assembly systems with higher-order growth kinetics.
我们提出了一种非线性杂交链式反应(HCR)系统,其中触发 DNA 引发被猝灭的双链底物自我持续组装成荧光树枝状纳米结构。在此过程中,越来越多原本被猝灭底物隔离的带有荧光报告基团的触发序列被释放出来,导致组装的 DNA 树枝状聚合物的链分支生长和荧光强度的指数增加。通过 PAGE 分析检查了触发组装行为,并通过 AFM 成像验证了生长的树枝状聚合物的形态。通过时间依赖性荧光光谱也证实了荧光积累的指数动力学。该方法采用了简单的序列设计策略,该概念可以适应具有更高阶生长动力学的组装系统。