4.8 Article

Direct dynamic read-out of molecular chirality with autonomous enzyme-driven swimmers

Journal

NATURE CHEMISTRY
Volume 13, Issue 12, Pages 1241-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41557-021-00798-9

Keywords

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Funding

  1. European Research Council under the European Union [741251]
  2. Universita degli Studi di Milano
  3. European Research Council (ERC) [741251] Funding Source: European Research Council (ERC)

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One key method for designing bioinspired machines is transferring concepts from nature to man-made structures by integrating biomolecules into artificial mechanical systems, allowing the conversion of molecular information into macroscopic action. Hybrid bioelectrochemical swimmers can convert chiral information into enantiospecific macroscopic trajectories, with potential biomedical applications and food quality testing.
A key approach for designing bioinspired machines is to transfer concepts from nature to man-made structures by integrating biomolecules into artificial mechanical systems. This strategy allows the conversion of molecular information into macroscopic action. Here, we describe the design and dynamic behaviour of hybrid bioelectrochemical swimmers that move spontaneously at the air-water interface. Their motion is governed by the diastereomeric interactions between immobilized enantiopure oligomers and the enantiomers of a chiral probe molecule present in solution. These dynamic bipolar systems are able to convert chiral information present at the molecular level into enantiospecific macroscopic trajectories. Depending on the enantiomer in solution, the swimmers will move clockwise or anticlockwise; the concept can also be used for the direct visualization of the degree of enantiomeric excess by analysing the curvature of the trajectories. Deciphering in such a straightforward way the enantiomeric ratio could be useful for biomedical applications, for the read-out of food quality or as a more general analogue of polarimetric measurements.

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