4.8 Article

A synthetic enzyme built from DNA flips 107 lipids per second in biological membranes

Journal

NATURE COMMUNICATIONS
Volume 9, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-04821-5

Keywords

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Funding

  1. National Science Foundation [DMR-1507985, PHY-1430124, EEC-1227034]
  2. National Institutes of Health [P41-GM104601, R01-GM116961]
  3. XSEDE Allocation Grant [MCA05S028]
  4. ERC consolidator grant [DesignerPores 647144]
  5. DAAD
  6. Winton Programme for the Physics of Sustainability
  7. Gates Cambridge
  8. Oppenheimer Ph.D. studentship
  9. EPSRC
  10. Cambridge Trust
  11. Direct For Mathematical & Physical Scien
  12. Division Of Materials Research [1507985] Funding Source: National Science Foundation
  13. Div Of Engineering Education and Centers
  14. Directorate For Engineering [1227034] Funding Source: National Science Foundation

Ask authors/readers for more resources

Mimicking enzyme function and increasing performance of naturally evolved proteins is one of the most challenging and intriguing aims of nanoscience. Here, we employ DNA nanotechnology to design a synthetic enzyme that substantially outperforms its biological archetypes. Consisting of only eight strands, our DNA nanostructure spontaneously inserts into biological membranes by forming a toroidal pore that connects the membrane's inner and outer leaflets. The membrane insertion catalyzes spontaneous transport of lipid molecules between the bilayer leaflets, rapidly equilibrating the lipid composition. Through a combination of microscopic simulations and fluorescence microscopy we find the lipid transport rate catalyzed by the DNA nanostructure exceeds 10(7) molecules per second, which is three orders of magnitude higher than the rate of lipid transport catalyzed by biological enzymes. Furthermore, we show that our DNA-based enzyme can control the composition of human cell membranes, which opens new avenues for applications of membrane-interacting DNA systems in medicine.

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