4.8 Article

Dissipative Constitutional Dynamic Networks for Tunable Transient Responses and Catalytic Functions

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 142, Issue 41, Pages 17480-17488

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c06977

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Funding

  1. Israel Science Foundation
  2. Minerva Center for Biohybrid Complex Systems

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Following the significance of dissipative, out-of-equilibrium biological processes controlling living systems, we introduce nucleic acid-based dissipative constitutional dynamic networks (CDNs) that exhibit tunable transient composition changes of the networks dictated by auxiliary fuel strands. CDN X composed of four equilibrated nucleic acid constituents, AA', AB', BA', and BB', and the accompanying dormant structures T1L1 and T2L2 and nicking enzyme Nt.BbvCI, undergoes dissipative orthogonal transitions to CDN Y and back or to CDN Z and back. In the presence of the fuel strand L-1' or L-2', the displacement of the respective dormant structure releases the trigger T-1 or T-2 that activates the reconfiguration of CDN X to CDN Y or CDN X to CDN Z. The generated duplex L1L1' or L2L2' is designed to be nicked by Nt.BbvCI, leading to the regeneration of L-1 or L-2 that rebinds to T-1 or T-2, resulting in the dissipative cyclic recovery of CDN X. Kinetic simulations of the dissipative processes allow us to predict the dissipative behavior of the systems under different auxiliary conditions. Subjecting CDN X to altering sets of the fuel strands L-1' and L-2' yields programmed reconfiguration patterns of dissipative reaction cycles. By engineering functional nucleic acid tethers on the constituents and the triggering strands, orthogonal dissipative emerging catalytic transformations dictated by the dissipative CDNs are demonstrated.

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