Materials Science and Engineering Program, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Nanoscale. 2015 Nov 7;7(41):17397-403. doi: 10.1039/c5nr05124j.
DNA can be manipulated to design nano-machines through specific sequence recognition. We report a switchable DNA carrier for repeatable capture and release of a single stranded DNA. The activity of the carrier was regulated by the interactions among a double-stranded actuator, single stranded target, fuel, and anti-fuel DNA strands. Inosine was used to maintain a stable triple-stranded complex when the actuator's conformation was switched between open (capture) and closed (release) configurations. Time lapse fluorescence measurements show repeatable capture and release of target strands. TEM images also show visible capture of target DNA strands when gold nanoparticles were attached to the DNA carrier and the target DNA strand. The carrier activity was controlled by length of toeholds, number of mismatches, and inosine substitutions. Significantly, unlike in previously published work that reported the devices functioned only when there is a perfect match between the interacting DNA strands, the present device works only when there are mismatches in the fuel strand and the best performance is achieved for 1-3 mismatches. The device was used to successfully capture and release gold nanoparticles when linked to the target single-stranded DNA. In general, this type of devices can be used for transport and delivery of theranostic molecules.
DNA 可以通过特定的序列识别来操纵,设计出纳米机器。我们报告了一种可切换的 DNA 载体,用于重复捕获和释放单链 DNA。该载体的活性通过双链激活剂、单链靶标、燃料和反燃料 DNA 链之间的相互作用来调节。当激活剂构象在打开(捕获)和关闭(释放)构型之间切换时,肌苷用于维持稳定的三链复合物。时间分辨荧光测量显示可重复的靶标链捕获和释放。TEM 图像还显示,当金纳米粒子附着在 DNA 载体和靶 DNA 链上时,可以明显捕获靶 DNA 链。载体活性受结合点长度、错配数和肌苷取代的控制。与以前发表的报道只有在相互作用的 DNA 链之间存在完美匹配时,该设备才能发挥作用的工作原理不同,本设备仅在燃料链中有错配时起作用,并且在 1-3 个错配时达到最佳性能。当与目标单链 DNA 连接时,该设备可成功捕获和释放金纳米粒子。总的来说,这种类型的设备可用于治疗药物分子的运输和递送。