Department of Chemistry and International Institute for Nanotechnology, Northwestern University , 2145 Sheridan Road, Evanston, Illinois 60208, United States.
NUANCE Center and Department of Materials Science and Engineering, Northwestern University , 2220 Campus Drive, Evanston, Illinois 60208-3108, United States.
J Am Chem Soc. 2015 Oct 21;137(41):13381-8. doi: 10.1021/jacs.5b08678. Epub 2015 Oct 12.
Two complementary small-molecule-DNA hybrid (SMDH) building blocks have been combined to form well-defined supramolecular cage dimers at DNA concentrations as high as 102 μM. This was made possible by combining a flexible small-molecule core and three DNA arms of moderate lengths (<20 base pairs). These results were successfully modeled by coarse-grained molecular dynamics simulations, which also revealed that the formation of ill-defined networks in the case of longer DNA arms can be significantly biased by the presence of deep kinetic traps. Notably, melting point studies revealed that cooperative melting behavior can be used as a means to distinguish the relative propensities for dimer versus network formation from complementary flexible three-DNA-arm SMDH (fSMDH3) components: sharp, enhanced melting transitions were observed for assemblies that result mostly in cage dimers, while no cooperative melting behavior was observed for assemblies that form ill-defined networks.
两种互补的小分子-DNA 杂合体(SMDH)构建模块已被组合在一起,以在高达 102μM 的 DNA 浓度下形成明确的超分子笼二聚体。这是通过将柔性小分子核心与三个适度长度的 DNA 臂(<20 个碱基对)结合来实现的。这些结果通过粗粒度分子动力学模拟成功建模,该模拟还表明,在较长 DNA 臂的情况下形成不明确的网络的情况可以通过存在深动力学陷阱而显著偏向。值得注意的是,熔点研究表明,协同熔融行为可用于区分互补的柔性三 DNA 臂 SMDH(fSMDH3)组件中二聚体与网络形成的相对倾向:对于主要形成笼二聚体的组装体,观察到尖锐、增强的熔融转变,而对于形成不明确网络的组装体,未观察到协同熔融行为。