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DNA origami has been able to controllably construct highly precise and complex two- or three-dimensional nanostructures of various morphologies. However, their application in the biosensing field is still relatively limited. In this paper, we proposed a portable electrochemical sensor for the detection of nucleic acid targets, using circulating tumor DNA (ctDNA) as an example. This biosensor combined DNA origami with high-curvature gold nanostructures. First, the target was captured by DNA origami in a homogeneous solution and formed the DNA origami-ctDNA (DOC) complex. Subsequently, the DOC complex was further brought to the electrode surface through hybridization with peptide nucleic acids (PNAs) modified on the surface of the gold nanostructures. The high-curvature nanostructured surface reduces entanglement and aggregation between the PNA probes, enhancing their accessibility to DOC. Furthermore, the substantial intrinsic charge of DNA origami can adsorb numerous electroactive [Ru(NH)], whereas PNAs are electrically neutral, significantly enhancing the detection sensitivity and reducing background signals, enabling ultrasensitive detection sensitivity. Additionally, we demonstrated that the DNA origami-based sensor enhanced signal amplification efficiency compared to single-stranded DNA and tetrahedral DNA nanostructures. Through this signal amplification strategy, the sensor achieves highly sensitive (0.26 fM), specific, and selective (in serum) detection of ctDNA, providing a new avenue for nonenzymatic signal amplification and expanding the application of DNA origami in the sensing field.
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http://dx.doi.org/10.1016/j.bios.2025.117692 | DOI Listing |
Nanoscale Horiz
September 2025
Programmable Biomaterials Laboratory, Institute of Materials, Interfaculty Bioengineering Institute, School of Engineering, Ecole Polytechnique Fédérale Lausanne, Lausanne, 1015, Switzerland.
The nanoscale spatial arrangement of T cell receptor (TCR) ligands critically influences their activation potential in CD8 T cells, yet a comprehensive understanding of the molecular landscape induced by engagement with native peptide-MHC class I (pMHC-I) remains incomplete. Using DNA origami nanomaterials, we precisely organize pMHC-I molecules into defined spatial configurations to systematically investigate the roles of valencies, inter-ligand spacings, geometric patterns, and molecular flexibility in regulating T cell function. We find that reducing the inter-ligand spacing to ∼7.
View Article and Find Full Text PDFAdv Drug Deliv Rev
September 2025
Biochemistry, CUNY Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY 10016, United States; Molecular, Cellular, and Developmental Biology, CUNY Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY 10016, United States; Chemistry, CUNY Gradua
Targeted drug delivery significantly enhances therapeutic efficacy across various diseases, particularly in cancer treatments, where conventional approaches such as chemotherapy and radiotherapy often cause severe side effects. In this context, nucleic acid aptamers-short, single-stranded DNA or RNA oligonucleotides capable of binding specific targets with high affinity-have emerged as promising tools for precision drug delivery and therapy. Aptamers can be selected against whole, living cells using SELEX and chemically modified for diverse applications.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Martin A. Fisher School of Physics, Brandeis University, Waltham, MA 02453.
Programmable self-assembly has recently enabled the creation of complex structures through precise control of the interparticle interactions and the particle geometries. Targeting ever more structurally complex, dynamic, and functional assemblies necessitates going beyond the design of the structure itself, to the measurement and control of the local flexibility of the intersubunit connections and its impact on the collective mechanics of the entire assembly. In this study, we demonstrate a method to infer the mechanical properties of multisubunit assemblies using cryogenic electron microscopy (cryo-EM) and RELION's multi-body refinement.
View Article and Find Full Text PDFSmall Methods
September 2025
Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China.
Natural polyreactive antibodies achieve enhanced avidity through heterogeneous ligand binding. However, engineering synthetic heteroligation systems with precise control over recognition motif orientation and distance remains challenging. Here, a DNA framework-based strategy is presented to program heterotypic binding by spatially organizing bivalent aptamers targeting platelet-derived growth factor-BB (PDGF-BB).
View Article and Find Full Text PDFACS Nano
September 2025
Department of Chemistry, Queen Mary University of London, Mile End Road, London E1 4NS, United Kingdom.
Nanoscale organization of integrin-mediated receptor crosstalk is crucial for controlling cellular signaling in cancer biology. Previously, interactions between integrin αvβ6 and receptor tyrosine kinases (RTKs) have been implicated in cancer progression, but the spatial regulatory mechanisms remain undefined. Here, we developed a programmable DNA origami-based platform for nanoscale control of heteroligand multivalency and spacing, enabling systematic investigation of αvβ6-RTK interactions in cancer biology.
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