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Programmable Enzymatic Reaction Network in Artificial Cell-Like Polymersomes.

Hanjin SeoHyomin Lee
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
The ability to precisely control in vitro enzymatic reactions in synthetic cells plays a crucial role in the bottom-up design of artificial cell models that can recapitulate the key cellular features and functions such as metabolism. However, integration of enzymatic reactions has been limited to bulk or microfluidic emulsions without a membrane, lacking the ability to design more sophisticated higher-order artificial cell communities for reconstituting spatiotemporal biological information at multiple length scales. Herein, droplet microfluidics is utilized to synthesize artificial cell-like polymersomes with distinct molecular permeability for spatiotemporal control of enzymatic reactions driven by external signals and fuels. The presence of a competing reverse enzymatic reaction that depletes the active substrates is shown to enable demonstration of fuel-driven formation of sub-microcompartments within polymersomes as well as realization of out-of-equilibrium systems. In addition, the different permeability characteristics of polymersome membranes are exploited to successfully construct a programmable enzymatic reaction network that mimics cellular communication within a heterogeneous cell community through selective molecular transport.
Keyphrases
  • single cell
  • hydrogen peroxide
  • cell therapy
  • healthcare
  • high throughput
  • nitric oxide
  • mesenchymal stem cells
  • single molecule
  • cell cycle arrest
  • circulating tumor cells