Dissipatively Fueled Unidirectionally Communicating DNA Circuits That Control Biocatalysis

P Philippe Jung (Institute of Technical and Macromolecular Chemistry RWTH Aachen University Aachen Germany) D Daniel Felder (DWI‐Leibniz Institute for Interactive Materials Aachen Germany) G Gurudas Chakraborty (DWI − Leibniz-Institute for Interactive Materials, Forckenbeckstraße 50, 52074 Aachen, Germany) T Tim Seifert (Institute of Technical and Macromolecular Chemistry RWTH Aachen University Aachen Germany) M Matthias Wessling (DWI‐Leibniz Institute for Interactive Materials Aachen Germany) L Lifei Zheng A Andreas Herrmann (Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074 Aachen, Germany)

Abstract

ABSTRACT Unlike most synthetic systems, life constantly reorganizes itself through the irreversible consumption of energy‐rich molecules and exhibits dynamic functionalities governed by spatiotemporally controlled biocatalytic processes. Inspired by this, we herein demonstrate unidirectionally communicating, out‐of‐equilibrium DNA circuits that enable network‐guided control of the biocatalytic activity of an enzyme. The unidirectional communication is realized through the programmed, dissipative manipulation of information transfer. In this process, transient activation of a DNAzyme generates the fuel required for the temporal activation of trypsin. Prior to establishing this information‐transfer framework, we employed fuel‐driven dissipation to autonomously and temporally regulate the activity of nucleic acid and protein‐based enzymes, each operating in individual cycles. The transient state of the systems is attained through rapid hybridization of DNA strands, while digestion of the DNA fuel by exonucleases regenerates the initial equilibrium state. These processes proceed in a cyclic manner, allowing the systems to attain an out‐of‐equilibrium state. Precise control over the lifetime of this transient state was achieved by regulating external factors, such as DNA fuel and exonuclease concentrations, and internally by exploiting the toe‐hold length‐dependent digestion kinetics of the exonucleases. To establish our findings, we adopted a combined approach that includes both experimental and computational methodologies.

Article Details

Volume / Issue Vol. 65, Issue 17
Published April 20, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

P

Philippe Jung

Institute of Technical and Macromolecular Chemistry RWTH Aachen University Aachen Germany

D

Daniel Felder

DWI‐Leibniz Institute for Interactive Materials Aachen Germany

G

Gurudas Chakraborty

DWI − Leibniz-Institute for Interactive Materials, Forckenbeckstraße 50, 52074 Aachen, Germany

T

Tim Seifert

Institute of Technical and Macromolecular Chemistry RWTH Aachen University Aachen Germany

M

Matthias Wessling

DWI‐Leibniz Institute for Interactive Materials Aachen Germany

L

Lifei Zheng

A

Andreas Herrmann

Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074 Aachen, Germany