A chemoenzymatic reaction-diffusion system with local inhibition and distal activation

Spatiotemporal gating in signal transduction and corresponding activation or inhibition of a biochemical pathway is the hallmark of biological functionality. Herein, through both experimental and computational approaches, we developed a synthetic system to mimic one of the key biological signaling events - local inhibition and distal (long-range) activation (LIDA). The basis of our system lies in the differential diffusivity of - (i) injected dormant activator or pro-activator (Pro-A, urea, fast to diffuse due to non-binding with nanoparticle (NP) in gel matrix) that converts to activator (A, ammonium bicarbonate) via an enzyme (urease) embedded in the hydrogel) and (ii) inhibitor (IN, adenosine triphosphate (ATP), diffusion restricted due to interaction with NP). Here A and IN act as the activator and inhibitor of a base-catalyzed proton transfer reaction in the gel matrix, respectively. The indispensability of ProA to A conversion during diffusion for efficient time-regulated LIDA effect has also been demonstrated. The ability to input spatial gating of pH and reaction activation can potentially be extrapolated to develop neuromorphic self-assembled systems with distal programmability.

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Publication Details

Journal
Nature Communications
Published
2025-11-12
DOI
https://doi.org/10.1038/s41467-025-65605-2
Citations
2
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
Field-Weighted Citation Impact
1.19

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article

A chemoenzymatic reaction-diffusion system with local inhibition and distal activation

Rishi Ram Mahato, Subhabrata Maiti, Nandha Kumar Ettikkan, Niranjani Adikessavane
2 citations
Nature Communications
Supramolecular Self-Assembly in Materials
1.19
article

A chemoenzymatic reaction-diffusion system with local inhibition and distal activation

Rishi Ram Mahato, Subhabrata Maiti, Nandha Kumar Ettikkan, Niranjani Adikessavane
article en
2 citations

Abstract

Spatiotemporal gating in signal transduction and corresponding activation or inhibition of a biochemical pathway is the hallmark of biological functionality. Herein, through both experimental and computational approaches, we developed a synthetic system to mimic one of the key biological signaling events - local inhibition and distal (long-range) activation (LIDA). The basis of our system lies in the differential diffusivity of - (i) injected dormant activator or pro-activator (Pro-A, urea, fast to diffuse due to non-binding with nanoparticle (NP) in gel matrix) that converts to activator (A, ammonium bicarbonate) via an enzyme (urease) embedded in the hydrogel) and (ii) inhibitor (IN, adenosine triphosphate (ATP), diffusion restricted due to interaction with NP). Here A and IN act as the activator and inhibitor of a base-catalyzed proton transfer reaction in the gel matrix, respectively. The indispensability of ProA to A conversion during diffusion for efficient time-regulated LIDA effect has also been demonstrated. The ability to input spatial gating of pH and reaction activation can potentially be extrapolated to develop neuromorphic self-assembled systems with distal programmability.

Nature CommunicationsVol. 16(1)
Indian Institute of Science Education and Research Mohali (IN), Plaksha University
Arthritis National Research Foundation, Council of Scientific and Industrial Research, India, Indian Institute of Science Education and Research Mohali
Openalex Percentile: Top 19%
Supramolecular Self-Assembly in Materials
1.19
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A chemoenzymatic reaction-diffusion system with local inhibition and distal activation — Rishi Ram Mahato, Subhabrata Maiti, et al. · Nature Communications (2025) | TGRS Research Map | TGRS