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DNAzyme- and light-induced dissipative and gated DNA networks

Nucleic acid-based dissipative, out-of-equilibrium systems are introduced as functional assemblies emulating transient dissipative biological transformations. One system involves a Pb 2+ -ion-dependent DNAzyme fuel strand-driven network leading to the transient cleavage of the fuel strand to "w...

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Bibliographic Details
Published in:Chemical science (Cambridge) 2021-08, Vol.12 (33), p.1124-11212
Main Authors: Wang, Jianbang, Li, Zhenzhen, Zhou, Zhixin, Ouyang, Yu, Zhang, Junji, Ma, Xiang, Tian, He, Willner, Itamar
Format: Article
Language:English
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Summary:Nucleic acid-based dissipative, out-of-equilibrium systems are introduced as functional assemblies emulating transient dissipative biological transformations. One system involves a Pb 2+ -ion-dependent DNAzyme fuel strand-driven network leading to the transient cleavage of the fuel strand to "waste" products. Applying the Pb 2+ -ion-dependent DNAzyme to two competitive fuel strand-driven systems yields two parallel operating networks. Blocking the competitively operating networks with selective inhibitors leads, however, to gated transient operation of dictated networks, yielding gated catalytic operations. A second system introduces a "non-waste" generating out-of-equilibrium, dissipative network driven by light. The system consists of a trans -azobenzene-functionalized photoactive module that is reconfigured by light to an intermediary state consisting of cis -azobenzene units that are thermally recovered to the original trans -azobenzene-modified module. The cyclic transient photoinduced operation of the device is demonstrated. The kinetic simulation of the systems allows the prediction of the transient behavior of the networks under different auxiliary conditions. Functional DNA modules are triggered in the presence of appropriate inhibitors to yield transient gated catalytic functions, and a photoresponsive DNA module leads to "waste-free" operation of transient, dissipative dynamic transitions.
ISSN:2041-6520
2041-6539
DOI:10.1039/d1sc02091a