Evidence map›Paper›PMID 40894727›Full record

ArticlebioRxiv : the preprint server for biology2025

High-speed 3D DNA PAINT and unsupervised clustering for unlocking 3D DNA origami cryptography.

Gde Bimananda Mahardika Wisna, Daria Sukhareva, Jonathan Zhao, Prathamesh Chopade, Deeksha Satyabola, Michael Matthies, Subhajit Roy, Chao Wang, Petr Šulc, Hao Yan and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

11 authors.

Gde Bimananda Mahardika WisnaDepartment of Physics, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0003-4463-944X
Daria SukharevaCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Jonathan ZhaoSchool of Molecular Sciences, Arizona State University, Tempe, Arizona, USA.
Prathamesh ChopadeCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0002-2825-6791
Deeksha SatyabolaCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0003-0960-8103
Michael MatthiesCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0001-5979-1757
Subhajit RoyDepartment of Physics, Arizona State University, Tempe, Arizona, USA.
Chao WangCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Petr ŠulcCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0003-1565-6769
Hao YanCenter for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Rizal F HariadiDepartment of Physics, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0001-7840-859X

Funding

Nanoscale reconstruction of mechanical systems involved in disease pathogenesisDP2AI144247 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI HARIADI, RIZAL FAJAR · 2018 to 2018
$2.4M
NIAID NIH HHS DP2 AI144247
6 · The paper itself

Abstract

DNA origami information storage is a promising alternative to silicon-based data storage, offering a secure molecular cryptography technique that conceals information within arbitrarily folded DNA origami nanostructures. Routing, sliding, and interlacing staple strands lead to the creation of a large 700-bit key size. The realization of practical DNA data storage requires high information density, robust security, and accurate and rapid information retrieval. To meet these requirements, advanced readout techniques and large encryption key sizes are essential. In this study, we report an enhanced DNA origami cryptography protocol to encrypt information in 2D and 3D DNA origami structures, increasing the number of possible scaffold routings and increasing the encryption key size. We employed all-DNA-based steganography with fast readout through high-speed 2D and 3D DNA-PAINT super-resolution imaging, which enables higher information density. By combining 2D and 3D DNA-PAINT data with unsupervised clustering, we achieved an accuracy of up to 89% and high ratios of correct-to-wrong readout, despite the significant flexibility in the 3D DNA origami structure shown by oxDNA simulation. Furthermore, we propose design criteria that ensure complete information retrieval for the DNA origami cryptography protocol. Our findings demonstrate that DNA-based cryptography is a highly secure and versatile solution for transmitting and storing information, making it an attractive choice for the post-silicon era.

Indexed as

3D DNA origami cryptography3D DNA origami storageHigh-speed DNA-PAINTunsupervised clustering

Identifiers

PMID40894727
PMCPMC12393260

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.