Physik-Department E14, Technische Universität München , 85748 Garching, Germany.
Nano Lett. 2016 Oct 12;16(10):6683-6690. doi: 10.1021/acs.nanolett.6b03586. Epub 2016 Sep 12.
DNA origami structures are artificial molecular nanostructures in which DNA double helices are forced into a closely packed configuration by a multitude of DNA strand crossovers. We show that three different types of origami structures (a flat sheet, a hollow tube, and a compact origami block) can be formed in magnesium-free buffer solutions containing low (<1 mM) concentrations of the condensing agent spermidine. Much like in DNA condensation, the amount of spermidine required for origami folding is proportional to the DNA concentration. At excessive amounts, the structures aggregate and precipitate. In contrast to origami structures formed in conventional buffers, the resulting structures are stable in the presence of high electric field pulses, such as those commonly used for electrotransfection experiments. We demonstrate that spermidine-stabilized structures are stable in cell lysate and can be delivered into mammalian cells via electroporation.
DNA 折纸结构是一种人工分子纳米结构,其中 DNA 双螺旋通过大量的 DNA 链交叉强制形成紧密堆积的构象。我们表明,在不含镁的缓冲溶液中,可以形成三种不同类型的折纸结构(平板、空心管和紧凑的折纸块),该缓冲溶液中含有低浓度(<1mM)的凝聚剂 spermidine。与 DNA 凝聚一样,用于折纸折叠的 spermidine 量与 DNA 浓度成正比。在过量的情况下,结构会聚集和沉淀。与在传统缓冲液中形成的折纸结构相比,在存在高电场脉冲的情况下,所得到的结构是稳定的,例如通常用于电转染实验的电场脉冲。我们证明,spermidine 稳定的结构在细胞裂解物中是稳定的,并可以通过电穿孔递送到哺乳动物细胞中。