Academic Journal

Programmable Nanoscale Motion via Molecular Patterning on DNA Origami

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Title: Programmable Nanoscale Motion via Molecular Patterning on DNA Origami
Authors: Paffen, Lars, Engelbert van Bevervoorde, Maurik, Rodriguez-Abetxuko, Andoni, Abdelmohsen, Loai, van der Hofstad, Remco, van Hest, Jan C.M., Patiño Padial, Tania
Source: Paffen, L, Engelbert van Bevervoorde, M, Rodriguez-Abetxuko, A, Abdelmohsen, L, van der Hofstad, R, van Hest, J C M & Patiño Padial, T 2026, 'Programmable Nanoscale Motion via Molecular Patterning on DNA Origami', Angewandte Chemie - International Edition, vol. 65, no. 8, e23921. https://doi.org/10.1002/anie.202523921
Publication Year: 2026
Subject Terms: DNA origami, Enzyme kinetics, Nanomotors, Single-particle tracking, Nanotubes/chemistry, Motion, DNA/chemistry, Urease/metabolism, Nanotechnology
Description: 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.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
ISSN: 1433-7851
1521-3773
Relation: info:eu-repo/semantics/altIdentifier/pmid/41546160; info:eu-repo/semantics/altIdentifier/pissn/1433-7851; info:eu-repo/semantics/altIdentifier/eissn/1521-3773
DOI: 10.1002/anie.202523921
Availability: https://research.tue.nl/en/publications/e2ba0223-bef4-438b-ad8a-3948f0457c0d
https://doi.org/10.1002/anie.202523921
https://pure.tue.nl/ws/files/381187458/Angew_Chem_Int_Ed_-_2026_-_Paffen_-_Programmable_Nanoscale_Motion_via_Molecular_Patterning_on_DNA_Origami.pdf
https://www.scopus.com/pages/publications/105027655065
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.97781BFB
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  Data: Programmable Nanoscale Motion via Molecular Patterning on DNA Origami
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  Data: <searchLink fieldCode="AR" term="%22Paffen%2C+Lars%22">Paffen, Lars</searchLink><br /><searchLink fieldCode="AR" term="%22Engelbert+van+Bevervoorde%2C+Maurik%22">Engelbert van Bevervoorde, Maurik</searchLink><br /><searchLink fieldCode="AR" term="%22Rodriguez-Abetxuko%2C+Andoni%22">Rodriguez-Abetxuko, Andoni</searchLink><br /><searchLink fieldCode="AR" term="%22Abdelmohsen%2C+Loai%22">Abdelmohsen, Loai</searchLink><br /><searchLink fieldCode="AR" term="%22van+der+Hofstad%2C+Remco%22">van der Hofstad, Remco</searchLink><br /><searchLink fieldCode="AR" term="%22van+Hest%2C+Jan+C%2EM%2E%22">van Hest, Jan C.M.</searchLink><br /><searchLink fieldCode="AR" term="%22Patiño+Padial%2C+Tania%22">Patiño Padial, Tania</searchLink>
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  Data: Paffen, L, Engelbert van Bevervoorde, M, Rodriguez-Abetxuko, A, Abdelmohsen, L, van der Hofstad, R, van Hest, J C M & Patiño Padial, T 2026, 'Programmable Nanoscale Motion via Molecular Patterning on DNA Origami', Angewandte Chemie - International Edition, vol. 65, no. 8, e23921. https://doi.org/10.1002/anie.202523921
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  Data: 2026
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  Data: <searchLink fieldCode="DE" term="%22DNA+origami%22">DNA origami</searchLink><br /><searchLink fieldCode="DE" term="%22Enzyme+kinetics%22">Enzyme kinetics</searchLink><br /><searchLink fieldCode="DE" term="%22Nanomotors%22">Nanomotors</searchLink><br /><searchLink fieldCode="DE" term="%22Single-particle+tracking%22">Single-particle tracking</searchLink><br /><searchLink fieldCode="DE" term="%22Nanotubes%2Fchemistry%22">Nanotubes/chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Motion%22">Motion</searchLink><br /><searchLink fieldCode="DE" term="%22DNA%2Fchemistry%22">DNA/chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Urease%2Fmetabolism%22">Urease/metabolism</searchLink><br /><searchLink fieldCode="DE" term="%22Nanotechnology%22">Nanotechnology</searchLink>
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  Data: 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.
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        Value: 10.1002/anie.202523921
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      – Text: English
    Subjects:
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        Type: general
      – SubjectFull: Enzyme kinetics
        Type: general
      – SubjectFull: Nanomotors
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      – SubjectFull: Single-particle tracking
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      – SubjectFull: Motion
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      – SubjectFull: Urease/metabolism
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      – TitleFull: Programmable Nanoscale Motion via Molecular Patterning on DNA Origami
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