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Efficient nanomedicine delivery across mucosal barriers remains a challenge due to the complex and poorly understood relationship between nanoparticle design and mucus transport. Here, we present DNA origami as a platform to investigate how the nanoparticle shape and ligand patterning influence diffusivity in mucus. By decoupling these parameters while maintaining identical material composition, we systematically evaluated the diffusion of rod, icosahedral, and rectangular nanostructures by using high-resolution single-particle tracking. Our results reveal that diffusivity in mucus is not solely determined by shape or functionalization alone but by their interplay: while unmodified rods diffused poorly, their mobility increased significantly upon antibody functionalization, reaching a maximum at an intermediate ligand density. In contrast, rods and icosahedra exhibited less pronounced and nonoptimal responses to surface modification. These findings highlight the importance of topology-specific optimization in nanoparticle design and demonstrate the utility of DNA nanotechnology to uncover design rules for next-generation mucus-penetrating drug delivery systems.
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http://dx.doi.org/10.1021/acs.nanolett.5c02352 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Institute of Materiobiology, College of Sciences, Shanghai University, Shanghai, 200444, China.
Self-assembled DNA nanostructures have been popularly used to develop DNA-based electrochemical sensors by exploiting the nanoscale positioning capability of DNA origami. However, the impact of the electric field on the structural stability of the DNA origami framework and the activity of carried DNA probes remains to be explored. Herein, we employ DNA origami as structural frameworks for reversible DNA hybridization, and develop a single-molecule fluorescence imaging method to quantify electric field effects on DNA conformation and hybridization properties at the single-molecule level.
View Article and Find Full Text PDFUnlabelled: Plasma membrane (PM) lipids and proteins are organized into nanoscale regions called nanodomains, which regulate essential cellular processes by controlling local membrane organization. Despite advances in super-resolution microscopy and single particle tracking, the small size and temporal instability of nanodomains make them difficult to study in living cells. To overcome these challenges, we built fluorescent DNA origami probes that insert into the PM via lipid anchors displayed on the cell.
View Article and Find Full Text PDFJ Control Release
September 2025
Institute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, PR China.
Structural DNA nanotechnology has emerged as a powerful tool in modern medicine, offering precise self-assembly and spatial programmability for the design of functional nanocarriers. DNA nanostructures can be categorized into one-dimensional (1D), two-dimensional (2D), and three-dimensional (3D) architectures, each with distinct advantages: 1D structures are suited for studying cellular responses to physical cues, 2D structures provide large surface areas for enhanced molecular recognition, and 3D structures enable improved cellular uptake and tissue penetration. Despite their potential, there is still no widespread consensus on the optimal structural design for specific diseases.
View Article and Find Full Text PDFAdv Drug Deliv Rev
September 2025
Department of Chemistry, Purdue University, West Lafayette 47907, IN 47907, USA. Electronic address:
DNA nanotechnology, a cutting-edge field that constructs sophisticated DNA-based nanostructures by harnessing the unparalleled programmability of DNA, has evolved into a powerful tool for applications in therapy, biosensing, logic computation, and more. This review outlines the fundamental strategies for constructing DNA nanostructures, beginning with the design of basic building blocks such as small, symmetric tiles (e.g.
View Article and Find Full Text PDFACS Nano
September 2025
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm 171 77, Sweden.
DNA origami-based nanotechnology is a versatile tool for exploring fundamental biological questions and holds significant promise for future biomedical applications. Here, we leverage the optical transparency of the embryonic zebrafish to analyze live embryos injected intravenously with fluorescently labeled wireframe DNA origami nanosheets. Our approach integrated long-term, high-resolution imaging of transgenic live zebrafish embryos with single-cell RNA sequencing to elucidate the effects of oligolysine-polyethylene glycol copolymer (K-PEG) coating on the biodistribution of fluorescence signal in embryos injected with wireframe DNA origami nanosheets.
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