In recent years, DNA has emerged as a promising molecule for the construction of molecular computing systems. In the research field of DNA logic circuits, enzyme-driven DNA logic circuits, which offer faster reactions and lower complexity, have become the key focus in the field. However, it remains a significant drawback that it lacks the capability of being reused. Reusability is essential to enhance the computational capacity, correct errors, and reduce costs in DNA circuits. In this study, we propose a method for achieving high reuse in enzyme-driven DNA logic circuits using exonuclease III. By selectively digesting ds-DNA while preserving gate strands, our system highly restores the circuit to its initial state, which contains no waste-strand. This reuse method has demonstrated good performance in the converted-input reuse experiment of single-gate, multilayer cascades. Finally, we achieve four times converted-input reuse in a relatively complex circuit and three times multiple reuse in a square root DNA circuit.
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http://dx.doi.org/10.1021/acsnano.4c15176 | DOI Listing |
Int J Mol Sci
February 2025
School of Mathematics, Physics and Statistics, Shanghai University of Engineering Science, Shanghai 201620, China.
DNA (Deoxyribonucleic Acid) logic circuit systems provide a powerful arithmetic architecture for the development of molecular computations. DNA nanotechnology, particularly DNA origami, provides a nanoscale addressable surface for DNA logic circuit systems. Although molecular computations based on DNA origami surfaces have received significant attention in research, there are still obstacles to constructing localized scalable DNA logic circuit systems.
View Article and Find Full Text PDFAcc Chem Res
March 2025
Center for BioEnergetics, Biodesign Institute and School of Molecular Sciences, Arizona State University, Tempe, Arizona 85287, United States.
ConspectusProteins and peptides occur ubiquitously in organisms and play key functional roles, as structural elements and catalysts. Their major natural source is ribosomal synthesis, which produces polypeptides from 20 amino acid building blocks. Peptides containing noncanonical amino acids have long been prepared by chemical synthesis, which has provided a wealth of physiologically active compounds.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
March 2025
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801.
Rapid and accurate detection of DNA from disease-causing pathogens is essential for controlling the spread of infections and administering timely treatments. While traditional molecular diagnostics techniques like PCR are highly sensitive, they include nucleic acid amplification and many need to be performed in centralized laboratories, limiting their utility in point-of-care settings. Recent advances in CRISPR-based diagnostics (CRISPR-Dx) have demonstrated the potential for highly specific molecular detection, but the sensitivity is often constrained by the slow trans-cleavage activity of Cas enzymes, necessitating preamplification of target nucleic acids.
View Article and Find Full Text PDFAnal Chem
March 2025
Key Laboratory of Green Chemistry & Technology, College of Chemistry, Sichuan University, Chengdu 610064, P.R. China.
DNA logic circuits have gained great success in the past, thanks to their distinct performance regarding the scalability and correctness of computation. However, there are still two challenges often considered for DNA logic circuit-based computation. First, the mainstream optical probes are often subject to spectral overlapping interference for complex multitask analysis and outputs.
View Article and Find Full Text PDFSci Adv
March 2025
School of Electronic Science and Engineering, Fujian Key Laboratory of Ultrafast Laser Technology and Applications, Xiamen University, Xiamen 361012, P. R. China.
Enzymatic nucleic acid reaction is a fundamental tool in molecular biology. However, high-complexity enzymatic DNA reactions and assays are still challenging due to the difficulties in integrating and scaling up microscale reaction units and mixing tools. Here, we present scalable acoustofluidic platform featuring acoustic virtual stirrer (AVS) arrays, serving as stirrers to increase the efficiency of interfacial enzymatic nucleic acid reactions.
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