Versatile and Programmable DNA Logic Gates on Universal and Label-Free Homogeneous Electrochemical Platform

2016 ◽  
Vol 88 (19) ◽  
pp. 9691-9698 ◽  
Author(s):  
Lei Ge ◽  
Wenxiao Wang ◽  
Ximei Sun ◽  
Ting Hou ◽  
Feng Li
Keyword(s):  
Small ◽  
2010 ◽  
Vol 6 (7) ◽  
pp. NA-NA
Author(s):  
Constantin Pistol ◽  
Vincent Mao ◽  
Viresh Thusu ◽  
Alvin R. Lebeck ◽  
Chris Dwyer

Nanomaterials ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 984 ◽  
Author(s):  
Victoria Goldsworthy ◽  
Geneva LaForce ◽  
Seth Abels ◽  
Emil Khisamutdinov

RNA aptamers that bind non-fluorescent dyes and activate their fluorescence are highly sensitive, nonperturbing, and convenient probes in the field of synthetic biology. These RNA molecules, referred to as light-up aptamers, operate as molecular nanoswitches that alter folding and fluorescence function in response to ligand binding, which is important in biosensing and molecular computing. Herein, we demonstrate a conceptually new generation of smart RNA nano-devices based on malachite green (MG)-binding RNA aptamer, which fluorescence output controlled by addition of short DNA oligonucleotides inputs. Four types of RNA switches possessing AND, OR, NAND, and NOR Boolean logic functions were created in modular form, allowing MG dye binding affinity to be changed by altering 3D conformation of the RNA aptamer. It is essential to develop higher-level logic circuits for the production of multi-task nanodevices for data processing, typically requiring combinatorial logic gates. Therefore, we further designed and synthetized higher-level half adder logic circuit by “in parallel” integration of two logic gates XOR and AND within a single RNA nanoparticle. The design utilizes fluorescence emissions from two different RNA aptamers: MG-binding RNA aptamer (AND gate) and Broccoli RNA aptamer that binds DFHBI dye (XOR gate). All computationally designed RNA devices were synthesized and experimentally tested in vitro. The ability to design smart nanodevices based on RNA binding aptamers offers a new route to engineer “label-free” ligand-sensing regulatory circuits, nucleic acid detection systems, and gene control elements.


2016 ◽  
Vol 52 (1) ◽  
pp. 179-182 ◽  
Author(s):  
Lijun Xu ◽  
Shanni Hong ◽  
Na Sun ◽  
Kewei Wang ◽  
Lu Zhou ◽  
...  

Berberine is reported as a light-up fluorescence ligand for i-motif structures, which enables the development of label-free DNA-based logic gates.


2010 ◽  
Vol 132 (25) ◽  
pp. 8557-8559 ◽  
Author(s):  
Fan Xia ◽  
Xiaolei Zuo ◽  
Renqiang Yang ◽  
Ryan J. White ◽  
Yi Xiao ◽  
...  

2016 ◽  
Vol 52 (2) ◽  
pp. 402-405 ◽  
Author(s):  
Sai Bi ◽  
Jiayan Ye ◽  
Ying Dong ◽  
Haoting Li ◽  
Wei Cao

A cascade recycling amplification (CRA) that implements cascade logic circuits with feedback amplification function is developed for label-free chemiluminescence detection of microRNA-122 with an ultrahigh sensitivity of 0.82 fM and excellent specificity, which is applied to construct a series of molecular-scale two-input logic gates by using microRNAs as inputs and CRA products as outputs.


2017 ◽  
Vol 53 (90) ◽  
pp. 12201-12204 ◽  
Author(s):  
Yongcun Yan ◽  
Shuzhen Yue ◽  
Tingting Zhao ◽  
Baoyu Luo ◽  
Sai Bi

A versatile exonuclease-assisted target recycling amplification strategy is demonstrated to achieve label-free chemiluminescence detection of DNA and construction of a series of two-input molecular logic gates.


Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2408
Author(s):  
Jingjing Zhang ◽  
Jialun Han ◽  
Shehong Feng ◽  
Chaoqun Niu ◽  
Chen Liu ◽  
...  

In this study, a target recycled amplification, background signal suppression, label-free fluorescent, enzyme-free deoxyribonucleic acid (DNA) machine was developed for the detection of adenosine triphosphate (ATP) in human urine. ATP and DNA fuel strands (FS) were found to trigger the operation of the DNA machine and lead to the cyclic multiplexing of ATP and the release of single stranded (SS) DNA. Double-stranded DNA (dsDNA) was formed on graphene oxide (GO) from the combination of SS DNA and complementary strands (CS′). These double strands then detached from the surface of the GO and in the process interacted with PicoGreen dye resulting in amplifying fluorescence intensity. The results revealed that the detection range of the DNA machine is from 100 to 600 nM (R2 = 0.99108) with a limit of detection (LOD) of 127.9 pM. A DNA machine circuit and AND-NOT-AND-OR logic gates were successfully constructed, and the strategy was used to detect ATP in human urine. With the advantage of target recycling amplification and GO suppressing background signal without fluorescent label and enzyme, this developed strategy has great potential for sensitive detection of different proteins and small molecules.


Biomaterials ◽  
2011 ◽  
Vol 32 (30) ◽  
pp. 7318-7324 ◽  
Author(s):  
Jinbo Zhu ◽  
Tao Li ◽  
Libing Zhang ◽  
Shaojun Dong ◽  
Erkang Wang
Keyword(s):  

2018 ◽  
Vol 9 (2) ◽  
pp. 300-306 ◽  
Author(s):  
Junhua Chen ◽  
Jiafeng Pan ◽  
Shu Chen

A complete set of elementary logic gates and two multilevel circuits have been constructed on a label-free and enzyme-free biocomputing platform using caged G-quadruplex as the signal transducer.


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