Small Molecule Release and Activation through DNA Computing

被引:46
作者
Morihiro, Kunihiko [1 ]
Ankenbruck, Nicholas [1 ]
Lukasak, Bradley [1 ]
Deiters, Alexander [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
基金
美国国家科学基金会;
关键词
NUCLEIC-ACID DETECTION; RATIOMETRIC FLUORESCENT-PROBE; ROLLING CIRCLE AMPLIFICATION; STRAND DISPLACEMENT CASCADES; LOGIC GATES; MAMMALIAN-CELLS; MESSENGER-RNA; LIVING CELLS; DRUG-RELEASE; IN-SITU;
D O I
10.1021/jacs.7b07831
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:13909 / 13915
页数:7
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