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Lectin-Glycan-Mediated Nanoparticle Docking as a Step towards Programmable Membrane Catalysis and Adhesion in Synthetic Protocells.

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The spontaneous assembly of nanoscale building blocks into continuous semi-permeable membranes is a key requirement for the structuration of synthetic protocells. Engineering the functionality and programmability of these building units… Click to show full abstract

The spontaneous assembly of nanoscale building blocks into continuous semi-permeable membranes is a key requirement for the structuration of synthetic protocells. Engineering the functionality and programmability of these building units provides a step towards more complex cell-like entities with adaptive membrane properties. Inspired by the central role of protein (lectin)-carbohydrate interactions in cellular recognition and adhesion, we fabricate semi-permeable polysaccharide-polymer microcapsules (polysaccharidosomes) with intrinsic lectin-binding properties. We employ amphiphilic polysaccharide-polymer membrane building blocks endowed with intrinsic bio-orthogonal lectin-glycan recognition sites to facilitate the reversible non-covalent docking of functionalized polymer or zeolitic nanoparticles on the polysaccharidosomes. We show that the programmed attachment of enzyme-loaded nanoparticles gives rise to a membrane-gated spatially localized cascade reaction within the protocells due to the thermoresponsiveness of the polysaccharidosome membrane, and demonstrate that extended closely packed networks are produced via reversible lectin-mediated adhesion between the protocells. Our results provide a step towards nanoscale engineering of bioinspired cell-like materials and could have longer term applications in synthetic virology, protobiology and micro-biosensor and micro-bioreactor technologies.

Keywords: synthetic protocells; lectin glycan; adhesion; step towards; membrane

Journal Title: ACS nano
Year Published: 2020

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