Compliant DNA Origami Nanoactuators as Size-Selective Nanopores

Journal Article (2024)
Author(s)

Ze Yu (TU Delft - Dynamics of Micro and Nano Systems)

Anna V. Baptist (Ludwig Maximilians University, Max Planck Institute of Biochemistry)

Susanne C.M. Reinhardt (Ludwig Maximilians University, Max Planck Institute of Biochemistry)

Eva Bertosin (Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

Cees Dekker (Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

Ralf Jungmann (Max Planck Institute of Biochemistry, Ludwig Maximilians University)

Amelie Heuer-Jungemann (Max Planck Institute of Biochemistry, Ludwig Maximilians University)

Sabina Caneva (TU Delft - Dynamics of Micro and Nano Systems)

DOI related publication
https://doi.org/10.1002/adma.202405104 Final published version
More Info
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Publication Year
2024
Language
English
Journal title
Advanced Materials
Issue number
39
Volume number
36
Article number
2405104
Downloads counter
309
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Abstract

Biological nanopores crucially control the import and export of biomolecules across lipid membranes in cells. They have found widespread use in biophysics and biotechnology, where their typically narrow, fixed diameters enable selective transport of ions and small molecules, as well as DNA and peptides for sequencing applications. Yet, due to their small channel sizes, they preclude the passage of large macromolecules, e.g., therapeutics. Here, the unique combined properties of DNA origami nanotechnology, machine-inspired design, and synthetic biology are harnessed, to present a structurally reconfigurable DNA origami MechanoPore (MP) that features a lumen that is tuneable in size through molecular triggers. Controllable switching of MPs between 3 stable states is confirmed by 3D-DNA-PAINT super-resolution imaging and through dye-influx assays, after reconstitution of the large MPs in the membrane of liposomes via an inverted-emulsion cDICE technique. Confocal imaging of transmembrane transport shows size-selective behavior with adjustable thresholds. Importantly, the conformational changes are fully reversible, attesting to the robust mechanical switching that overcomes pressure from the surrounding lipid molecules. These MPs advance nanopore technology, offering functional nanostructures that can be tuned on-demand – thereby impacting fields as diverse as drug delivery, biomolecule sorting, and sensing, as well as bottom-up synthetic biology.