Scalable Logic Circuits with Multiple Outputs and an Automatic Reset Function Based on DNAzyme-Mediated Branch Migration.

Anal Chem

National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-Environmental Pollution Control and Management, Institute of Eco-Environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou 510650, China.

Published: February 2021

AI Article Synopsis

  • A multilayer DNA circuit platform was developed using lead (Pb), copper (Cu), and zinc (Zn) as inputs and producing three distinct fluorescent outputs.
  • The logic network functions like a molecular keypad lock, utilizing DNAzyme-guided cleavage and toehold-mediated strand migration for secure information protection, with a monitoring system that identifies correct password entries.
  • The platform features an autonomous reset function due to the autocatalytic nature of DNAzyme, allowing it to maintain robustness and effectiveness in complex environmental conditions.

Article Abstract

A scalable logic platform made up of multilayer DNA circuits was constructed using Pb, Cu, and Zn as the three inputs and three different fluorescent signals as the outputs. DNAzyme-guided cyclic cleavage reactions and DNA toehold-mediated strand branch migration were utilized to organize and connect nucleic acid probes for building the high-level logic architecture. The sequence communications between each circuit enable the logic network to work as a keypad lock, which is an information protection model at the molecular level. The multi-output mode was used to monitor the gradual unlocking process of the security system, from which one can determine which password is correct or not immediately. The autocatalytic cleavage of DNAzyme makes the biocomputing circuit feasible to realize the reset function automatically without external stimuli. Importantly, the logic platform is robust and can work effectively even in complex environmental samples.

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Source
http://dx.doi.org/10.1021/acs.analchem.0c05173DOI Listing

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