ArticleNano letters2026
Vesicle-Templated Self-Assembly of Programmable Freestanding Multi-μm DNA Shells.
Article in Nano letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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0 citing papers in PubMed.
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Authors and funding
3 authors.
Funding
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Abstract
In the quest to create increasingly complex synthetic cell-mimicking systems, diverse DNA nanostructures have been developed to coat, permeabilize, sculpt, or otherwise functionalize lipid vesicles or used as scaffolds to direct vesicle growth. Here, we introduce a simple, broadly applicable method to realize freestanding, membrane-mimicking DNA shells: DNA shells are first assembled on giant unilamellar vesicles and then liberated by surfactant-mediated liposome removal, retaining the geometry of their membrane templates. We demonstrate this approach using two distinct DNA tecton classes: a complex barrel-shaped DNA origami and a simple 11-oligonucleotide nanostar-inspired motif. The site-specific addressability of DNA origami structures enables the rational design of binding interfaces, as demonstrated by the controlled formation of multilayer shells. The success of both strategies underscores the feasibility of using different DNA architectures to create tunable, DNA-only shell-like compartments spanning the size range of eukaryotic cells, thereby offering a fundamentally new type of compartmentalization for bottom-up synthetic biology.
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