Evidence map›Paper›PMID 42185313›Full record

ArticleNature communications2026

De novo design of DNA origami with a generative diffusion model.

Chien Truong-Quoc, Kyounghwa Jeon, Jinho Kim, Seo Hyun Kwon, Dongsik Seo, Chanseok Lee, Do-Nyun Kim

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Chien Truong-Quoc *Department of Mechanical Engineering, Seoul National University, Gwanak-gu, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0001-6219-1322
Kyounghwa Jeon *Department of Mechanical Engineering, Seoul National University, Gwanak-gu, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-2020-9736
Jinho KimDepartment of Mechanical Engineering, Seoul National University, Gwanak-gu, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0004-4302-9863
Seo Hyun KwonDepartment of Mechanical Engineering, Seoul National University, Gwanak-gu, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0005-4735-8004
Dongsik SeoDepartment of Mechanical Engineering, Seoul National University, Gwanak-gu, Seoul, Republic of Korea.
Chanseok LeeSchool of Bio-Pharmaceutical Convergence, Hanyang University, Sangnok-gu, Ansan, Republic of Korea. chanseok@hanyang.ac.kr.ORCID http://orcid.org/0000-0002-7969-4345
Do-Nyun KimDepartment of Mechanical Engineering, Seoul National University, Gwanak-gu, Seoul, Republic of Korea. dnkim@snu.ac.kr.ORCID http://orcid.org/0000-0003-0896-4552

Funding

National Research Foundation of Korea (NRF) RS-2024-00346176National Research Foundation of Korea (NRF) RS-2026-25490531
6 · The paper itself

Abstract

Generative models that have advanced inverse design in protein engineering can be extended to DNA origami to explore broader design spaces enabling complex geometries and functions for emerging nanotechnologies. However, progress in generative DNA origami design has been limited by the lack of large, standardized structural datasets containing structural information. To address this challenge, we introduce a diffusion-based generative design framework trained on simulated equilibrium conformations obtained using a multiscale computational model. Given user-defined target geometries, our model produces physically plausible DNA origami designs through guided diffusion sampling and strand routing, with integrated structure prediction for quantitative evaluation. Among more than 100 generated candidates, selected structures are experimentally validated, demonstrating proper folding and functional behaviors such as auxetic transformation and modular assembly. Our results highlight the potential of generative modeling for complex DNA origami design, expanding the accessible design space and facilitating the creation of sophisticated, reconfigurable architectures.

Indexed as

DNANucleic Acid ConformationComputer SimulationDiffusionDNA NanostructuresGenerative Artificial IntelligenceModels, MolecularNanotechnologyDNA

Identifiers

PMID42185313
PMCPMC13385962

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.