Department of Chemistry, Physical Chemistry, University of Potsdam, Karl-Liebknecht Str. 24-25, 14476 Potsdam, Germany.
Nanoscale. 2016 May 21;8(19):10339-47. doi: 10.1039/c6nr00119j. Epub 2016 May 3.
The folding of single-stranded telomeric DNA into guanine (G) quadruplexes is a conformational change that plays a major role in sensing and drug targeting. The telomeric DNA can be placed on DNA origami nanostructures to make the folding process extremely selective for K(+) ions even in the presence of high Na(+) concentrations. Here, we demonstrate that the K(+)-selective G-quadruplex formation is reversible when using a cryptand to remove K(+) from the G-quadruplex. We present a full characterization of the reversible switching between single-stranded telomeric DNA and G-quadruplex structures using Förster resonance energy transfer (FRET) between the dyes fluorescein (FAM) and cyanine3 (Cy3). When attached to the DNA origami platform, the G-quadruplex switch can be incorporated into more complex photonic networks, which is demonstrated for a three-color and a four-color FRET cascade from FAM over Cy3 and Cy5 to IRDye700 with G-quadruplex-Cy3 acting as a switchable transmitter.
单链端粒 DNA 折叠成鸟嘌呤 (G) 四链体是一种构象变化,在感应和药物靶向中起着重要作用。端粒 DNA 可以被放置在 DNA 折纸纳米结构上,使折叠过程在存在高浓度 Na+ 的情况下对 K+ 离子具有极高的选择性。在这里,我们证明了当使用 cryptand 将 K+ 从 G-四联体中去除时,K+ 选择性 G-四联体的形成是可逆的。我们使用荧光素 (FAM) 和 Cy3 之间的Förster 共振能量转移 (FRET) 对单链端粒 DNA 和 G-四联体结构之间的可逆转换进行了全面表征。当连接到 DNA 折纸平台时,G-四联体开关可以被整合到更复杂的光子网络中,这在一个三色和四色 FRET 级联中得到了证明,从 FAM 到 Cy3 和 Cy5 再到 IRDye700,G-四联体-Cy3 作为可切换的发射器。