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   <dc:title>Sustained, Reversible, and Adaptive Non-Equilibrium Steady States of a Dissipative DNA-Based System</dc:title>
   <dc:creator>Nicholas, James D.</dc:creator>
   <dc:creator>Grosso, Erica del</dc:creator>
   <dc:creator>deMello, Andrew J.</dc:creator>
   <dc:creator>Puigmartí-Luis, Josep</dc:creator>
   <dc:creator>Ricci, Francesco, 1977-</dc:creator>
   <dc:creator>Sorrenti, Alessandro</dc:creator>
   <dc:subject>Àcids nucleics</dc:subject>
   <dc:subject>Biologia sintètica</dc:subject>
   <dc:subject>Nucleic acids</dc:subject>
   <dc:subject>Synthetic biology</dc:subject>
   <dc:description>Inspired by nature, researchers have developed several chemical fuel-driven supramolecular systems aimed at achieving improved kinetic control over their formation and functions. Alongside, DNA-based systems regulated by energy-dissipating mechanisms have been reported. However, the majority of these systems rely on batchwise additions of chemical fuels to closed reactors, resulting in transient non-equilibrium states that differ fundamentally from the sustained and highly adaptable non-equilibrium steady states (NESS) maintained by living systems through continuous energy dissipation. Here, we demonstrate sustained NESS of a dissipative DNA strand-displacement reaction achieved through the continuous supply of an RNA fuel to an open semi-batch reactor, using a custom automated setup that enables tunable fuel infusion rates and in situ analysis. Similar to biological NESS, our system dynamically adapts in real-time to subtle variations in fuel supply, achieving different steady-state levels of the strand-displacement reaction. Our approach demonstrates remarkable on-the-fly control over a dissipative DNA nanosystem, unachievable when working under batch conditions. Importantly, by fitting the experimental data to a kinetic model of the reaction network, we were able to confirm that the observed steady states correspond to true non-equilibrium compositions of the system.</dc:description>
   <dc:date>2025-12-04T13:53:50Z</dc:date>
   <dc:date>2025-12-04T13:53:50Z</dc:date>
   <dc:date>2025-10-20</dc:date>
   <dc:date>2025-12-04T13:53:51Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>1433-7851</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/224681</dc:identifier>
   <dc:identifier>762131</dc:identifier>
   <dc:identifier>40884021</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1002/anie.202512967</dc:relation>
   <dc:relation>Angewandte Chemie-International Edition, 2025, vol. 64, num. 43</dc:relation>
   <dc:relation>https://doi.org/10.1002/anie.202512967</dc:relation>
   <dc:rights>cc-by-nc (c) Nicholas, James D. et al., 2025</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>8 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Wiley-VCH</dc:publisher>
   <dc:source>Articles publicats en revistes (Ciència dels Materials i Química Física)</dc:source>
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