Photoactivated Enzymatic Reaction Network Enables Spatiotemporal Programming of Thiol/Disulfide Redox Systems

Implementing photoactivation into chemical reaction networks (CRNs) offers opportunities for on-demand and remote activation, fuel storage, creating autonomous materials and systems with precise spatial activation. However, examples in this domain remain limited. Here, we introduce a cascaded redox-based enzymatic reaction network (ERN) capable of photoinitiation and refueling, centered around dissipative aromatic disulfide bond formation. To achieve photoinitiation, we integrate an upstream enzymatic module (EM) into the ERN, where the substrate of the EM can be photouncaged using blue light irradiation. A downstream regeneration system enhances the robustness of the reducing environment for repeated fueling. This cascaded ERN operates in solution, allowing for controlled dissipative disulfide formation while avoiding short-circuit reactions (SCR) between the oxidative and reductive halves of the reaction cycle. To showcase the utility of this photoactivated ERN, we couple it with aromatic thiol-terminated star polymers (sPEG-ArSH) to enable spatiotemporally controlled dissipative hydrogel formation using lithographic masks.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-04-07
DOI
https://doi.org/10.1002/anie.202503822
Citations
5
Primary Topic
Innovative Microfluidic and Catalytic Techniques Innovation
Type
article
Field-Weighted Citation Impact
3.37
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article

Photoactivated Enzymatic Reaction Network Enables Spatiotemporal Programming of Thiol/Disulfide Redox Systems

Lea Duttenhofer, Andreas Walther, Piet J. M. Swinkels, Aritra Sarkar et al.
5 citations
Angewandte Chemie International Edition
Innovative Microfluidic and Catalytic Techniques Innovation
3.37
article

Photoactivated Enzymatic Reaction Network Enables Spatiotemporal Programming of Thiol/Disulfide Redox Systems

Lea Duttenhofer, Andreas Walther, Piet J. M. Swinkels, Aritra Sarkar, Pol Besenius
article en
5 citations

Abstract

Implementing photoactivation into chemical reaction networks (CRNs) offers opportunities for on-demand and remote activation, fuel storage, creating autonomous materials and systems with precise spatial activation. However, examples in this domain remain limited. Here, we introduce a cascaded redox-based enzymatic reaction network (ERN) capable of photoinitiation and refueling, centered around dissipative aromatic disulfide bond formation. To achieve photoinitiation, we integrate an upstream enzymatic module (EM) into the ERN, where the substrate of the EM can be photouncaged using blue light irradiation. A downstream regeneration system enhances the robustness of the reducing environment for repeated fueling. This cascaded ERN operates in solution, allowing for controlled dissipative disulfide formation while avoiding short-circuit reactions (SCR) between the oxidative and reductive halves of the reaction cycle. To showcase the utility of this photoactivated ERN, we couple it with aromatic thiol-terminated star polymers (sPEG-ArSH) to enable spatiotemporally controlled dissipative hydrogel formation using lithographic masks.

Angewandte Chemie International EditionVol. 64(25)
Johannes Gutenberg University Mainz (DE)
Openalex Percentile: Top 8%
Innovative Microfluidic and Catalytic Techniques Innovation
3.37
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Photoactivated Enzymatic Reaction Network Enables Spatiotemporal Programming of Thiol/Disulfide Redox Systems — Lea Duttenhofer, Andreas Walther, et al. · Angewandte Chemie International Edition (2025) | TGRS Research Map | TGRS