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Scalable and sustainable manufacturing of functional DNA nanoassemblies via self-folding circular single-stranded DNA
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  • Published: 18 May 2026

Scalable and sustainable manufacturing of functional DNA nanoassemblies via self-folding circular single-stranded DNA

  • Tingting Zhai1,2 na1,
  • Siwen Liu3 na1,
  • Dantong Lei1 na1,
  • Ting Song4 na1,
  • Rachel Chun-Yee Tam3 na1,
  • Mingying Chen4,
  • Jialu Zhang1,
  • Jiangchao Qian  ORCID: orcid.org/0000-0002-0316-29595,
  • Chunhai Fan  ORCID: orcid.org/0000-0002-7171-73381,6,7,
  • Honglin Chen  ORCID: orcid.org/0000-0001-5108-83383,
  • Yanling Song  ORCID: orcid.org/0000-0002-6793-66854 &
  • …
  • Hongzhou Gu  ORCID: orcid.org/0000-0001-5058-48151,2,6,7 

Nature Communications (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Bacteriophages
  • DNA nanostructures
  • Nanobiotechnology
  • Synthesis and processing

Abstract

Functional DNA nanoassemblies (fDns) hold promise for biomedical and translational applications, but broader deployment is limited by manufacturing barriers that constrain scalability, reproducibility, and stability. Current biosynthetic approaches rely heavily on downstream enzymatic processing and purification, which dominate economic, operational, and environmental costs at scale. Here we report an integrated manufacturing strategy that combines programmed circular single-stranded DNA with bacteriophage-driven biosynthesis to enable direct production of high-quality fDns with minimal post-assembly purification. By reducing reliance on purification as a major bottleneck, this approach delivers topology-enhanced stability, high assembly efficiency, and batch reproducibility, achieving sub-gram laboratory production at ~$6 per milligram while suggesting a pathway toward scalable manufacturing. We demonstrate versatility through 11 distinct fDns, including an aptamer-functionalized construct that neutralizes SARS-CoV-2 pseudovirus and authentic Omicron variants in cellular and animal models. This work provides a cost-effective, scalable manufacturing framework for fDns, advancing their sustainable and reproducible deployment across life-science applications.

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Acknowledgements

This research is supported by Shanghai Municipal Science and Technology Major Project, Shanghai Pilot Program for Basic Research, and is part of the CREATE Thematic Programme in Decarbonisation (Carbon Negative Synthetic Biology for Biomaterial Production from CO2, CNSB), supported by the National Research Foundation, Prime Minister’s Office, Singapore under its Campus for Research Excellence and Technological Enterprise (CREATE) programme. The authors gratefully acknowledge Prof. Hui Lv and Xinbo Wang for their assistance with sequencing data analysis, and Instrumental Analysis Center of Shanghai Jiao Tong University for the assistance with Cryo-EM characterization.

Funding

H.G. discloses support for the research of this work from the National Natural Science Foundation of China [22525404, 82121002, U24A20377] and the Autonomous Project of State Key Laboratory of Synergistic Chem-Bio Synthesis [sklscbs202570]. Y.S. discloses support for the research of this work from the National Natural Science Foundation of China [22474115, 22022409], the Fujian Provincial Natural Science Foundation of China [2024J011006], and the Scientific Research Foundation of State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory [2025XAKJ0201001]. T.Z. discloses support for the research of this work from the National Natural Science Foundation of China [22304115, 82120108010]. H.C. discloses support for the research of this work from the Theme-Based Research Scheme [T11-709/21-N], Commissioned Research on the Novel Coronavirus Disease (COVID-19) [COVID190123], and the Emergency Collaborative Project of Guangzhou Laboratory, China [EKPG22-01]. J.Z. discloses support for the research of this work from the Postdoctoral Fellowship Program of CPSF [GZB20240431]. C.F. discloses support for the research and publication of this work from the National Natural Science Foundation of China [T2188102].

Author information

Author notes
  1. These authors contributed equally: Tingting Zhai, Siwen Liu, Dantong Lei, Ting Song, Rachel Chun-Yee Tam.

Authors and Affiliations

  1. State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, and the International Peace Maternity and Child Health Hospital, School of Medicine, National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai, 200030, China

    Tingting Zhai, Dantong Lei, Jialu Zhang, Chunhai Fan & Hongzhou Gu

  2. Department of Multidisciplinary Consultant Center, Shanghai Key Laboratory of Craniomaxillofacial Development and Diseases, Shanghai Stomatological Hospital & School of Stomatology, Fudan University, Shanghai, 200001, China

    Tingting Zhai & Hongzhou Gu

  3. State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, The University of Hong Kong, Hong Kong SAR, China

    Siwen Liu, Rachel Chun-Yee Tam & Honglin Chen

  4. The MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, the Key Laboratory of Chemical Biology of Fujian Province, Department of Chemical Biology, College of Chemistry and Chemical Engineering, State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiamen University, Fujian, 361005, China

    Ting Song, Mingying Chen & Yanling Song

  5. State Key Laboratory of Bioreactor Engineering, East China University of Science & Technology, Shanghai, 200237, China

    Jiangchao Qian

  6. SJTU Asia-Pacific Graduate Institute (SJTU-APGI), 1 Create Way, #14-01 CREATE Tower, Singapore, 138602, Singapore

    Chunhai Fan & Hongzhou Gu

  7. Xiangfu Laboratory, Jiashan, 314102, China

    Chunhai Fan & Hongzhou Gu

Authors
  1. Tingting Zhai
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  2. Siwen Liu
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  3. Dantong Lei
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  4. Ting Song
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  5. Rachel Chun-Yee Tam
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  6. Mingying Chen
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  7. Jialu Zhang
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  8. Jiangchao Qian
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  9. Chunhai Fan
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  10. Honglin Chen
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  11. Yanling Song
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  12. Hongzhou Gu
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Corresponding authors

Correspondence to Honglin Chen, Yanling Song or Hongzhou Gu.

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The authors declare no competing interests.

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Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Cite this article

Zhai, T., Liu, S., Lei, D. et al. Scalable and sustainable manufacturing of functional DNA nanoassemblies via self-folding circular single-stranded DNA. Nat Commun (2026). https://doi.org/10.1038/s41467-026-73464-8

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  • Received: 15 April 2026

  • Accepted: 13 May 2026

  • Published: 18 May 2026

  • DOI: https://doi.org/10.1038/s41467-026-73464-8

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