Engineering high-robustness DNA molecular circuits by utilizing nucleases. Issue 13 (20th March 2020)

• Record Type: Journal Article
• Authors: Fu, Shengnan; Li, Na; Li, Junjie; Deng, Yingnan; Xu, Lida; Yu, Changyuan; Su, Xin
• Is Part Of: Nanoscale. Volume 12:Issue 13(2020)
• Page Start: 6964
• Page End: 6970
• Publication Date: 2020-03-20
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c9nr09979d
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : We utilized site-specific and sequence-independent nucleases to engineer high-robustness DNA molecular circuits. Abstract : Toehold-mediated strand displacement (TMSD) as an important player in DNA nanotechnology has been widely utilized for engineering non-enzymatic molecular circuits. However, these circuits suffer from uncontrollable leakage and unsatisfactory response speed. We utilized site-specific and sequence-independent nucleases to engineer high- robustness DNA molecular circuits. First, we found that the kinetics of the APE1-catalyzed reaction is highly dependent on substrate stability, allowing for the elimination of asymptotic leakage of DNA split circuits. Second, we obtained strict substrate preference of λ exonuclease ( λ exo ) by optimizing the reaction conditions. Robust single-layer and cascade gates with leak resistance were established by using λ exo. Owing to the remarkably fast kinetics of these nucleases, all the circuits yield a high speed of computation. Compared to TMSD-based approaches, nuclease-powered circuits render advanced features such as leakage resistance, hundreds of times higher speed, and simplified structures, representing a class of promising artificial molecule systems.