Programmable Nanoscale Motion via Molecular Patterning on DNA Origami

L Lars Paffen (Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands) M Maurik Engelbert van Bevervoorde (Department of Mathematics and Computer Science Institute for Complex Molecular Systems Eindhoven University of Technology Metaforum, P. O. Box 513 Eindhoven 5600 MB The Netherlands) A Andoni Rodriguez‐Abetxuko (Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands) L Loai Abdelmohsen (Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands) R Remco van der Hofstad (Department of Mathematics and Computer Science Institute for Complex Molecular Systems Eindhoven University of Technology Metaforum, P. O. Box 513 Eindhoven 5600 MB The Netherlands) J Jan C.M. van Hest (Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands) T Tania Patiño Padial (Bio-Organic Chemistry, Departments of Biomedical Engineering and Chemical Engineering & Chemistry, Institute for Complex Molecular Systems)

Abstract

Abstract Asymmetry in enzymatically driven nanomotor design, both structural and functional, is widely considered essential for propulsion. However, the interplay between particle geometry, enzyme distribution, and catalytic loading remains poorly defined, largely due to limited control over enzyme positioning that hinders quantitative analysis. Using DNA origami nanorods, we achieve precise spatial placement of urease enzymes with independently tunable coverage and asymmetry. Single‐particle tracking reveals that motility arises not solely from enzyme number or spatial arrangement but from a balance between catalytic loading and geometric anisotropy. Unexpectedly, maximal propulsion occurs at ∼25% urease end‐coverage, significantly below the conventional 50% end‐coverage, where half of the available binding positions on one structural half of the origami are occupied. Boundary Element Method simulations incorporating identical spatial parameters reproduce these findings, confirming that programmable enzyme patterning dictates diffusiophoretic propulsion. These results provide a quantitative framework linking topology, catalytic activity, and motion, revealing that optimal motility does not coincide with maximal asymmetry and advancing the rational design of enzyme‐powered DNA nanomotors.

Article Details

Volume / Issue Vol. 65, Issue 8
Published February 16, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

L

Lars Paffen

Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands

M

Maurik Engelbert van Bevervoorde

Department of Mathematics and Computer Science Institute for Complex Molecular Systems Eindhoven University of Technology Metaforum, P. O. Box 513 Eindhoven 5600 MB The Netherlands

A

Andoni Rodriguez‐Abetxuko

Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands

L

Loai Abdelmohsen

Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands

R

Remco van der Hofstad

Department of Mathematics and Computer Science Institute for Complex Molecular Systems Eindhoven University of Technology Metaforum, P. O. Box 513 Eindhoven 5600 MB The Netherlands

J

Jan C.M. van Hest

Department of Biomedical Engineering and Chemical Engineering and Chemistry Institute for Complex Molecular Systems Eindhoven University of Technology Helix, P. O. Box 513 Eindhoven 5600 MB The Netherlands

T

Tania Patiño Padial

Bio-Organic Chemistry, Departments of Biomedical Engineering and Chemical Engineering & Chemistry, Institute for Complex Molecular Systems