Programmable DNA shell scaffolds for directional membrane budding

In the pursuit of replicating biological processes at the nanoscale, controlling cellular membrane dynamics has emerged as a key area of interest. Here, we report a system mimicking virus assembly to control directional membrane budding. We employ three-dimensional DNA origami techniques to construct cholesterol-modified triangles that self-assemble into polyhedral shells on lipid vesicles, resulting in gradual curvature induction, bud formation, and spontaneous neck scission. Strategic positioning of cholesterols on the triangle surface provides control over the directionality of bud growth and yields daughter vesicles with DNA endo- or exoskeletons reminiscent of clathrin-coated vesicles. This process occurs with rapid kinetics and across various lipid compositions. When combined into a two-step process, nested bivesicular objects with DNA shells encapsulated between lipid vesicles could be produced. Our work replicates key aspects of natural endocytic and exocytic pathways, opening new avenues for exploring membrane mechanics and applications in targeted drug delivery and synthetic biology.

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Publication Details

Journal
Nature Communications
Published
2025-10-09
DOI
https://doi.org/10.1038/s41467-025-64298-x
Citations
2
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
1.61

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article

Programmable DNA shell scaffolds for directional membrane budding

Hendrik Dietz, Michael T. Pinner
2 citations
Nature Communications
Advanced biosensing and bioanalysis techniques
1.61
article

Programmable DNA shell scaffolds for directional membrane budding

Hendrik Dietz, Michael T. Pinner
article en
2 citations

Abstract

In the pursuit of replicating biological processes at the nanoscale, controlling cellular membrane dynamics has emerged as a key area of interest. Here, we report a system mimicking virus assembly to control directional membrane budding. We employ three-dimensional DNA origami techniques to construct cholesterol-modified triangles that self-assemble into polyhedral shells on lipid vesicles, resulting in gradual curvature induction, bud formation, and spontaneous neck scission. Strategic positioning of cholesterols on the triangle surface provides control over the directionality of bud growth and yields daughter vesicles with DNA endo- or exoskeletons reminiscent of clathrin-coated vesicles. This process occurs with rapid kinetics and across various lipid compositions. When combined into a two-step process, nested bivesicular objects with DNA shells encapsulated between lipid vesicles could be produced. Our work replicates key aspects of natural endocytic and exocytic pathways, opening new avenues for exploring membrane mechanics and applications in targeted drug delivery and synthetic biology.

Nature CommunicationsVol. 16(1)
Technical University of Munich (DE)
European Commission, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Gottfried Wilhelm Leibniz Universität Hannover, Leibniz-Gemeinschaft
Openalex Percentile: Top 14%
Advanced biosensing and bioanalysis techniques
1.61
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Programmable DNA shell scaffolds for directional membrane budding — Hendrik Dietz, Michael T. Pinner · Nature Communications (2025) | TGRS Research Map | TGRS