Light-activated signaling in DNA-encoded sender-receiver architectures
Autor: | Iuliia Myrgorodska, Pascal A. Pieters, Bas W. A. Bögels, Alex Joesaar, Rens Brouwers, Tom F. A. de Greef, Shuo Yang, Stephen Mann |
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Přispěvatelé: | Chemical Biology, Computational Biology, ICMS Core |
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Protocell
Computer science Artificial cells Microfluidics microfluidics General Physics and Astronomy Cell Communication 02 engineering and technology 010402 general chemistry Network topology 01 natural sciences Signal Article Diffusion Synthetic biology Max Planck Bristol General Materials Science Communication source Molecular communication Artificial cell molecular communication Bristol BioDesign Institute General Engineering DNA 021001 nanoscience & nanotechnology 0104 chemical sciences DNA strand displacement circuits synthetic biology 0210 nano-technology Biological system Signal Transduction artificial cells |
Zdroj: | Yang, S, Pieters, P A, Joesaar, A, Bögels, B W A, Brouwers, R, Myrgorodska, I, Mann, S & Greef, T F A D 2020, ' Light-Activated Signaling in DNA-Encoded Sender–Receiver Architectures ', ACS Nano, vol. 14, no. 11, pp. 15992–16002 . https://doi.org/10.1021/acsnano.0c07537, https://doi.org/10.1021/acsnano.0c07537 ACS Nano ACS Nano, 14(11). American Chemical Society |
ISSN: | 1936-0851 |
DOI: | 10.1021/acsnano.0c07537 |
Popis: | Collective decision making by living cells is facilitated by exchange of diffusible signals where sender cells release a chemical signal that is interpreted by receiver cells. A variety of nonliving artificial cell models have been developed in recent years that mimic various aspects of diffusion-based intercellular communication. However, localized secretion of diffusive signals from individual protocells, which is critical for mimicking biological sender-receiver systems, has remained challenging to control precisely. Here, we engineer light-responsive, DNA-encoded sender-receiver architectures, where protein-polymer microcapsules act as cell mimics and molecular communication occurs through diffusive DNA signals. We prepare spatial distributions of sender and receiver protocells using a microfluidic trapping array and set up a signaling gradient from a single sender cell using light, which activates surrounding receivers through DNA strand displacement. Our systematic analysis reveals how the effective signal range of a single sender is determined by various factors including the density and permeability of receivers, extracellular signal degradation, signal consumption, and catalytic regeneration. In addition, we construct a three-population configuration where two sender cells are embedded in a dense array of receivers that implement Boolean logic and investigate spatial integration of nonidentical input cues. The results offer a means for studying diffusion-based sender-receiver topologies and present a strategy to achieve the congruence of reaction-diffusion and positional information in chemical communication systems that have the potential to reconstitute collective cellular patterns. |
Databáze: | OpenAIRE |
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