Ultra-fast Isothermal Formation of DNA Nanostructures in Culture Media: Application to in situ Assembly of DNA Origami with Living Cells

25 November 2025, Version 2
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

Synthetic DNA strands are programmable and biocompatible building blocks that can be combined through hybridization to form user-defined nanostructures, but their assembly traditionally requires cell-incompatible conditions, imposing a lengthy ex situ fabrication step before any application with living matter. Here we demonstrate for the first time that two- (2D) and three-dimensional (3D) DNA origami structures can isothermally self-assemble at 37 °C within minutes, directly in cell culture media, both in the absence and in the presence of living cells. Longer assembly times also enable the obtention of scaffold-free structures of extended dimensions, such as micrometer-long DNA nanotubes. With human cell lines, 2D and 3D origami structures in situ self-assemble in 5 to 15 min, and remain stable for about 24 h and up to 3 days when actin monomers are added. Similar self-assembly performance is observed in the presence of more complex tissue-like systems, such as human induced pluripotent stem cells evolving into cerebral organoids. This ultra-fast, life-compatible self-assembly method drastically simplifies the fabrication of complex DNA nanostructures and enables the creation of in situ self-assembling nanomachines for direct and adaptive interactions with living cells.

Keywords

DNA
Origami
Self-assembly
Nanomachine
Cell
Isothermal assembly
Ultra-fast assembly
Biological interface
Living system
Cell culture
Organoid
iPSC
Brain-on-chip
Cerebral organoid
HEK

Supplementary materials

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Supporting Information
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This file includes: 1. Materials 2. Methods 3. Supplementary figures S1–S16 4. Supplementary tables S1-S3 5. Supplementary references
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Movie S1
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Fluorescence microscopy observation of DNA nanotubes in solution obtained using 5 DNA oligonucleotides (500 nM each) forming a double-crossover (DX) in DMEM and left for isothermal self-assembly at 37 °C overnight.
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