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Exerting pulling forces in fluids by directional disassembly of microcrystalline fibres.

L C PantaleoneE CalicchiaJ MartinelliMarc C A StuartY Y LopatinaWesley R BrowneGiuseppe PortaleKatarzyna M TychTibor Kudernac
Published in: Nature nanotechnology (2024)
Biomolecular polymerization motors are biochemical systems that use supramolecular (de-)polymerization to convert chemical potential into useful mechanical work. With the intent to explore new chemomechanical transduction strategies, here we show a synthetic molecular system that can generate forces via the controlled disassembly of self-organized molecules in a crystal lattice, as they are freely suspended in a fluid. An amphiphilic monomer self-assembles into rigid, high-aspect-ratio microcrystalline fibres. The assembly process is regulated by a coumarin-based pH switching motif. The microfibre crystal morphology determines the monomer reactivity at the interface, resulting in anisotropic etching. This effect exerts a directional pulling force on microscopic beads adsorbed on the crystal surface through weak multivalent interactions. We use optical-tweezers-based force spectroscopy to extract mechanistic insights into this process, quantifying a stall force of 2.3 pN (±0.1 pN) exerted by the ratcheting mechanism produced by the disassembly of the microfibres.
Keyphrases
  • single molecule
  • solid state
  • high resolution
  • molecularly imprinted
  • oxidative stress
  • high speed
  • mass spectrometry
  • risk assessment
  • quantum dots
  • water soluble