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Small Molecule Release and Activation through DNA Computing
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2017-09-25 , DOI: 10.1021/jacs.7b07831
Kunihiko Morihiro 1 , Nicholas Ankenbruck 1 , Bradley Lukasak 1 , Alexander Deiters 1
Affiliation  

DNA-based logic gates can be assembled into computational devices that generate a specific output signal in response to oligonucleotide input patterns. The ability to interface with biological and chemical environments makes DNA computation a promising technology for monitoring cellular systems. However, DNA logic gate circuits typically provide a single-stranded oligonucleotide output, limiting the ability to effect biology. Here, we introduce a novel DNA logic gate design capable of yielding a small molecule output signal. Employing a Staudinger reduction as a trigger for the release and activation of a small molecule fluorophore, we constructed AND and OR logic gates that respond to synthetic microRNA (miRNA) inputs. Connecting the gates in series led to more complex DNA circuits that provided a small molecule output in response to a specific pattern of three different miRNAs. Moreover, our gate design can be readily multiplexed as demonstrated by simultaneous small molecule activation from two independent DNA circuits.

中文翻译:

通过 DNA 计算释放和激活小分子

基于 DNA 的逻辑门可以组装到计算设备中,这些设备会根据寡核苷酸输入模式生成特定的输出信号。与生物和化学环境交互的能力使 DNA 计算成为监测细胞系统的有前途的技术。然而,DNA 逻辑门电路通常提供单链寡核苷酸输出,限制了影响生物学的能力。在这里,我们介绍了一种能够产生小分子输出信号的新型 DNA 逻辑门设计。使用施陶丁格还原作为小分子荧光团释放和激活的触发器,我们构建了响应合成 microRNA (miRNA) 输入的 AND 和 OR 逻辑门。将门串联连接导致更复杂的 DNA 电路,提供小分子输出以响应三种不同 miRNA 的特定模式。此外,我们的门设计可以很容易地进行多路复用,正如来自两个独立 DNA 电路的同时小分子激活所证明的那样。
更新日期:2017-09-25
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