Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Oct 8;6(1):351.
doi: 10.1038/s41392-021-00727-9.

The biological applications of DNA nanomaterials: current challenges and future directions

Affiliations
Review

The biological applications of DNA nanomaterials: current challenges and future directions

Wenjuan Ma et al. Signal Transduct Target Ther. .

Abstract

DNA, a genetic material, has been employed in different scientific directions for various biological applications as driven by DNA nanotechnology in the past decades, including tissue regeneration, disease prevention, inflammation inhibition, bioimaging, biosensing, diagnosis, antitumor drug delivery, and therapeutics. With the rapid progress in DNA nanotechnology, multitudinous DNA nanomaterials have been designed with different shape and size based on the classic Watson-Crick base-pairing for molecular self-assembly. Some DNA materials could functionally change cell biological behaviors, such as cell migration, cell proliferation, cell differentiation, autophagy, and anti-inflammatory effects. Some single-stranded DNAs (ssDNAs) or RNAs with secondary structures via self-pairing, named aptamer, possess the ability of targeting, which are selected by systematic evolution of ligands by exponential enrichment (SELEX) and applied for tumor targeted diagnosis and treatment. Some DNA nanomaterials with three-dimensional (3D) nanostructures and stable structures are investigated as drug carrier systems to delivery multiple antitumor medicine or gene therapeutic agents. While the functional DNA nanostructures have promoted the development of the DNA nanotechnology with innovative designs and preparation strategies, and also proved with great potential in the biological and medical use, there is still a long way to go for the eventual application of DNA materials in real life. Here in this review, we conducted a comprehensive survey of the structural development history of various DNA nanomaterials, introduced the principles of different DNA nanomaterials, summarized their biological applications in different fields, and discussed the current challenges and further directions that could help to achieve their applications in the future.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
The biological applications of various DNA-based and DNA-encoding nanomaterials in tissue engineering. a, f The biological applications of different DNA-based nanomaterials in neural tissue (e.g., TDNs, NPs loading various pDNA, polycation loading various pDNA, and some nanofibrous loading pDNA). b The biological applications of different DNA-based nanomaterials in skin tissue (e.g., TDNs, polycation loading various pDNA, and some basement materials loading pDNA). c, e The biological applications of different DNA-based nanomaterials in skeletal and cardiac muscle engineering (e.g., skeletal tissue: NIR-DA, NPs loading genomic DNA, and various polycation loading pDNA; cardiac muscle: nanofibrous loading pDNA and TDNs). d The biological applications of different DNA-based nanomaterials in corneal tissue (e.g., TDNs, NPs loading various pDNA, and polycation loading various pDNA). g The biological applications of different DNA-based nanomaterials in bone tissue engineering (e.g., TDNs, LNPs loading pDNA, polypeptides loading various pDNA, and polycation loading various pDNA)
Fig. 2
Fig. 2
The fate of DNA materials following delivery into cells. Nucleic acid nanomaterials (e.g., TDNs, pDNA, ssDNA, and dsDNA) with the excellent ability to enter cells, can be internalized by cells and degraded by lysosomal. Nucleic acid cargos combine the DNA materials and different delivery systems. These vectors can protect the DNA materials from degradation and promote cellular internalization. When inside the cells, these vector-DNA material complexes are embedded in an endosome, and these vectors can help DNA materials to escape lysosomal degradation
Fig. 3
Fig. 3
DNA-based nanostructures on tumor therapy by modification with drug, aptamer, or other functional ligands act various biological functions, which can bind to the target protein of cells. DNA-based nanostructures could distinguish cancer cells via ligand-receptor binding and permeate the membranes through endocytosis. The corresponding release of therapeutical agents would cause cellular damage and lead to apoptosis of cancer cells
Fig. 4
Fig. 4
DNA-based nanostructures on immunostimulatory reactions. CpG-modified DNA-based nanostructures could enter immune cells, including macrophages, mast, dendritic and monocyte cells through integrating with TLR9, which subsequently induce cascade reactions and promote the secretion of remarkable cytokines and chemokines
Fig. 5
Fig. 5
DNA-based nanostructures on bioimaging and diagnosis. Targeted ligands (e.g., affibody, peptides and aptamers) and cargoes (e.g., drugs, fluorescein and radioisotopes) were simultaneously attached to DNA-based nanostructures. After specific combination with biomarkers, the integrates entered target cells and released fluorescent labels to sensitively detect the diseased regions

Similar articles

Cited by

References

    1. Dong Y, et al. DNA functional materials assembled from branched DNA: design, synthesis, and applications. Chem. Rev. 2020;120:9420–9481. doi: 10.1021/acs.chemrev.0c00294. - DOI - PubMed
    1. Broker TR, Lehman IR. Branched DNA molecules: intermediates in T4 recombination. J. Mol. Biol. 1971;60:131–149. doi: 10.1016/0022-2836(71)90453-0. - DOI - PubMed
    1. Seeman NC. DNA nanotechnology: from the pub to information-based chemistry. Methods Mol. Biol. 2018;1811:1–9. doi: 10.1007/978-1-4939-8582-1_1. - DOI - PubMed
    1. Seeman NC. DNA nanotechnology: novel DNA constructions. Annu. Rev. Biophys. Biomol. Struct. 1998;27:225–248. doi: 10.1146/annurev.biophys.27.1.225. - DOI - PubMed
    1. Seeman NC, Sleiman HF. DNA nanotechnology. Nat. Rev. Mater. 2018;3:17068. doi: 10.1038/natrevmats.2017.68. - DOI

Publication types