Catalytic Reconfiguration of Meta-DNA Assemblies

Bioinspired nanorobots rely on autonomous structural reconfiguration to adapt to environmental cues, yet achieving such behavior remains difficult due to an intrinsic trade-off between structural robustness and rapid responsiveness. Here, we present a reconfiguration strategy that leverages toehold-mediated strand displacement reactions within structurally stable meta-DNA (M-DNA) assemblies. Coupling this strategy with cooperative DNA catalysis accelerates reconfiguration by more than an order of magnitude, reducing the reconfiguration time from over 12 h to less than 2 h and achieving a maximum rate constant of 1.88 × 10<sup>5</sup> M<sup>-1</sup> s<sup>-1</sup>. Molecular dynamics simulations reveal that M-DNA catalytic reconfiguration occurs via cooperative multivalent pathways, enabling efficient strand displacement and structural reconfiguration. Furthermore, by integrating modular design with catalytic acceleration, we achieve rapid and programmable reconfigurations across hierarchical M-DNA assemblies. This strategy overcomes the intrinsic trade-off between structural robustness and dynamic adaptability in submicron DNA assemblies, establishing a generalizable principle for engineering adaptive biomimetic nanostructures.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-03-16
DOI
https://doi.org/10.1021/jacs.6c01421
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
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article

Catalytic Reconfiguration of Meta-DNA Assemblies

Qinglong Yan, Zhengwu Liang, Qin Xu, Meiyuan Qi et al.
Journal of the American Chemical Society
Advanced biosensing and bioanalysis techniques
article

Catalytic Reconfiguration of Meta-DNA Assemblies

Qinglong Yan, Zhengwu Liang, Qin Xu, Meiyuan Qi, Jinyang Lv, Tao Fan, Mingdong Li, Chunhai Fan, Guangbao Yao, Qien Shi
article en

Abstract

Bioinspired nanorobots rely on autonomous structural reconfiguration to adapt to environmental cues, yet achieving such behavior remains difficult due to an intrinsic trade-off between structural robustness and rapid responsiveness. Here, we present a reconfiguration strategy that leverages toehold-mediated strand displacement reactions within structurally stable meta-DNA (M-DNA) assemblies. Coupling this strategy with cooperative DNA catalysis accelerates reconfiguration by more than an order of magnitude, reducing the reconfiguration time from over 12 h to less than 2 h and achieving a maximum rate constant of 1.88 × 10<sup>5</sup> M<sup>-1</sup> s<sup>-1</sup>. Molecular dynamics simulations reveal that M-DNA catalytic reconfiguration occurs via cooperative multivalent pathways, enabling efficient strand displacement and structural reconfiguration. Furthermore, by integrating modular design with catalytic acceleration, we achieve rapid and programmable reconfigurations across hierarchical M-DNA assemblies. This strategy overcomes the intrinsic trade-off between structural robustness and dynamic adaptability in submicron DNA assemblies, establishing a generalizable principle for engineering adaptive biomimetic nanostructures.

Journal of the American Chemical SocietyVol. 148(11)
Macau University of Science and Technology (MO), Shanghai Jiao Tong University (CN), Jiaxing University (CN), Center for Translational Molecular Medicine (NL), Institute for Advanced Study (DE)
Openalex Percentile: Top 20%
Advanced biosensing and bioanalysis techniques
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