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通过 DNA 计算实现小分子的释放和激活。

Small Molecule Release and Activation through DNA Computing.

机构信息

Department of Chemistry, University of Pittsburgh , Pittsburgh, Pennsylvania 15260, United States.

出版信息

J Am Chem Soc. 2017 Oct 4;139(39):13909-13915. doi: 10.1021/jacs.7b07831. Epub 2017 Sep 25.

Abstract

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.

摘要

基于 DNA 的逻辑门可以组装成计算设备,这些设备可以根据寡核苷酸输入模式生成特定的输出信号。与生物和化学环境接口的能力使 DNA 计算成为监测细胞系统的一种很有前途的技术。然而,DNA 逻辑门电路通常提供单链寡核苷酸输出,限制了对生物学的影响。在这里,我们引入了一种新的 DNA 逻辑门设计,能够产生小分子输出信号。我们使用施蒂丁格还原作为小分子荧光团释放和激活的触发,构建了响应合成 microRNA (miRNA) 输入的与门和或门。将门串联起来,形成了更复杂的 DNA 电路,这些电路可以根据三种不同 miRNA 的特定模式提供小分子输出。此外,我们的门设计可以很容易地进行多重化,如通过来自两个独立的 DNA 电路的同时小分子激活来证明。

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