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T7 RNA polymerase non-specifically transcribes and induces disassembly of DNA nanostructures

机译:T7 RNA聚合酶非特异性转录并诱导DNA纳米结构的拆卸

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The use of proteins that bind and catalyze reactions with DNA alongside DNA nanostructures has broadened the functionality of DNA devices. DNA binding proteins have been used to specifically pattern and tune structural properties of DNA nanostructures and polymerases have been employed to directly and indirectly drive structural changes in DNA structures and devices. Despite these advances, undesired and poorly understood interactions between DNA nanostructures and proteins that bind DNA continue to negatively affect the performance and stability of DNA devices used in conjunction with enzymes. A better understanding of these undesired interactions will enable the construction of robust DNA nanostructure-enzyme hybrid systems. Here, we investigate the undesired disassembly of DNA nanotubes in the presence of viral RNA polymerases (RNAPs) under conditions used for in vitro transcription. We show that nanotubes and individual nanotube monomers (tiles) are non-specifically transcribed by T7 RNAP, and that RNA transcripts produced during non-specific transcription disassemble the nanotubes. Disassembly requires a single-stranded overhang on the nanotube tiles where transcripts can bind and initiate disassembly through strand displacement, suggesting that single-stranded domains on other DNA nanostructures could cause unexpected interactions in the presence of viral RNA polymerases.
机译:使用与DNA沿着DNA纳米结构结合和催化反应的蛋白质已经扩大了DNA器件的功能。已使用DNA结合蛋白特异性,并且已经使用DNA纳米结构和聚合酶的结构性质直接和间接地驱动DNA结构和装置的结构变化。尽管有这些预处理,但结合DNA与酶的DNA纳米结构和蛋白质之间的相互作用不希望地影响与酶结合使用的DNA装置的性能和稳定性。更好地理解这些不期望的相互作用将能够构建鲁棒DNA纳米结构 - 酶混合系统。这里,我们在用于体外转录的条件下研究病毒RNA聚合酶(RNAAPS)的存在下不希望的DNA纳米管。我们表明纳米管和单独的纳米管单体(瓦片)由T7 RNAP非特异性转录,并且在非特异性转录期间产生的RNA转录物拆卸纳米管。拆卸需要在纳米管瓷砖上进行单链悬垂,其中转录物可以通过链位移结合和引发拆卸,表明其他DNA纳米结构上的单链域可能导致病毒RNA聚合酶存在下的意外相互作用。

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