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In vitro selection of pH-activated DNA nanostructures

机译:pH活化DNA纳米结构的体外选择

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摘要

We report the first in vitro selection of DNA nanostructures that switch their conformation when triggered by change in pH. Previously, most pH-active nanostructures were designed using known pH-active motifs, such as the i-motif or the triplex structure. In contrast, we performed de novo selections starting from a random library and generated nanostructures that can sequester and release Mipomersen, a clinically approved antisense DNA drug, in response to pH change. We demonstrate extraordinary pH-selectivity, releasing up to 714-fold more Mipomersen at pH 5.2 compared to pH 7.5. Interestingly, none of our nanostructures showed significant sequence similarity to known pH-sensitive motifs, suggesting that they may operate via novel structure-switching mechanisms. We believe our selection scheme is general and could be adopted for generating DNA nanostructures for many applications including drug delivery, sensors and pH-active surfaces.
机译:我们报告了首次体外选择的DNA纳米结构,当pH值变化触发时会切换其构象。以前,大多数pH活性纳米结构都是使用已知的pH活性基序设计的,例如i-基序或三重结构。相反,我们从随机库中进行了从头选择,并生成了纳米结构,该纳米结构可以响应pH值的变化而螯合和释放Mipomersen(一种临床认可的反义DNA药物)。我们展示了非凡的pH选择性,与pH 7.5相比,pH 5.2释放的Mipomersen多达714倍。有趣的是,我们的纳米结构均未显示出与已知的pH敏感基序的显着序列相似性,这表明它们可能通过新颖的结构转换机制起作用。我们认为,我们的选择方案是通用的,可被用于生成DNA纳米结构,用于许多应用,包括药物输送,传感器和pH活性表面。

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