Electrochemical label-free biomolecular logic gates regulated by distinct inputs

2022 ◽  
pp. 114000
Author(s):  
Xinmei Song ◽  
Cuiyun Yang ◽  
Ruo Yuan ◽  
Yun Xiang
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.


Sensors ◽  
2019 ◽  
Vol 19 (24) ◽  
pp. 5409 ◽  
Author(s):  
Filip Kveton ◽  
Anna Blsakova ◽  
Lenka Lorencova ◽  
Monika Jerigova ◽  
Dusan Velic ◽  
...  

The study describes development of a glycan biosensor for detection of a tumor-associated antibody. The glycan biosensor is built on an electrochemically activated/oxidized graphene screen-printed electrode (GSPE). Oxygen functionalities were subsequently applied for covalent immobilization of human serum albumin (HSA) as a natural nanoscaffold for covalent immobilization of Thomsen-nouvelle (Tn) antigen (GalNAc-O-Ser/Thr) to be fully available for affinity interaction with its analyte—a tumor-associated antibody. The step by step building process of glycan biosensor development was comprehensively characterized using a battery of techniques (scanning electron microscopy, atomic force microscopy, contact angle measurements, secondary ion mass spectrometry, surface plasmon resonance, Raman and energy-dispersive X-ray spectroscopy). Results suggest that electrochemical oxidation of graphene SPE preferentially oxidizes only the surface of graphene flakes within the graphene SPE. Optimization studies revealed the following optimal parameters: activation potential of +1.5 V vs. Ag/AgCl/3 M KCl, activation time of 60 s and concentration of HSA of 0.1 g L−1. Finally, the glycan biosensor was built up able to selectively and sensitively detect its analyte down to low aM concentration. The binding preference of the glycan biosensor was in an agreement with independent surface plasmon resonance analysis.


2020 ◽  
Vol 154 ◽  
pp. 112050 ◽  
Author(s):  
Mateusz Śmietana ◽  
Marcin Koba ◽  
Petr Sezemsky ◽  
Katarzyna Szot-Karpińska ◽  
Dariusz Burnat ◽  
...  

2016 ◽  
Vol 88 (19) ◽  
pp. 9691-9698 ◽  
Author(s):  
Lei Ge ◽  
Wenxiao Wang ◽  
Ximei Sun ◽  
Ting Hou ◽  
Feng Li
Keyword(s):  

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.


2013 ◽  
Vol 27 ◽  
pp. 104-107 ◽  
Author(s):  
Jan Vacek ◽  
Martina Zatloukalova ◽  
Marika Havlikova ◽  
Jitka Ulrichova ◽  
Martin Kubala

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

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