Li Lin, An Ran, Tang Jiaxuan, Sui Zhe, Wang Guoqing, Komiyama Makoto, Liang Xingguo
College of Food Science and Engineering, Ocean University of China, Nucleic acids Chemistry and Biotechnology Laboratory, Shinan-qu, Qingdao, China.
College of Food Science and Engineering, Ocean University of China, Nucleic acids Chemistry and Biotechnology Laboratory, Shinan-qu, Qingdao, China; Laboratory for Marine Drugs and Bioproducts, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.
Biophys J. 2020 Apr 7;118(7):1702-1708. doi: 10.1016/j.bpj.2020.02.006. Epub 2020 Feb 15.
During the preparation of single-stranded DNA catenanes, topological isomers of different linking numbers (Lk) are intrinsically produced, and they must be separated from each other to construct sophisticated nanostructures accurately. In many previous studies, however, mixtures of these isomers were directly employed to construct nanostructures without sufficient characterization. Here, we present a method that easily and clearly characterizes the isomers by polyacrylamide gel electrophoresis. To the mixtures of topological isomers of [2]catenanes, two-strut oligonucleotides, which are complementary with a part of both rings, were added to connect the rings and fix the whole conformations of isomers. As a result, the order of migration rate was always Lk3 > Lk2 > Lk1, irrespective of gel concentration. Thus, all the topological isomers were unanimously characterized by only one polyacrylamide gel electrophoresis experiment. Well-characterized DNA catenanes are obtainable by this two-strut strategy, opening the way to more advanced nanotechnology.
在制备单链DNA连环体的过程中,会天然产生不同连接数(Lk)的拓扑异构体,为了精确构建复杂的纳米结构,必须将它们彼此分离。然而,在许多先前的研究中,这些异构体的混合物未经充分表征就直接用于构建纳米结构。在此,我们提出一种通过聚丙烯酰胺凝胶电泳轻松且清晰地表征这些异构体的方法。对于[2]连环体的拓扑异构体混合物,添加与两个环的一部分互补的双支柱寡核苷酸,以连接环并固定异构体的整体构象。结果,无论凝胶浓度如何,迁移速率的顺序始终是Lk3 > Lk2 > Lk1。因此,仅通过一次聚丙烯酰胺凝胶电泳实验就能一致地表征所有拓扑异构体。通过这种双支柱策略可获得表征良好的DNA连环体,为更先进的纳米技术开辟了道路。