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Herein, a supramolecular DNA nanodevice was formed via the rolling circle amplification (RCA) and hybridization chain reaction (HCR) cascade reaction on a tetrahedral DNA nanostructure (TDN) to achieve simultaneous sensitive detection and intracellular imaging of dual-miRNAs related to liver cancer. The supramolecular DNA nanodevice effectively addressed the limitations of low probe loading capacity in traditional TDN nanodevices by enriching plenty of signal probes around a single TDN, significantly enhancing the fluorescence signal. Impressively, the supramolecular DNA nanodevice with a TDN fulcrum and dense DNA structure imparted the nanodevice with strong rigidity, ensuring the stability of the signal probes to decrease aggregation quenching for further increasing the fluorescence response. Consequently, the biosensor based on supramolecular DNA nanodevice enabled simultaneous and sensitive detection of miRNA221 and miRNA222, and further achieved accurate in situ intracellular imaging of miRNA221 and miRNA222, displaying significantly improved imaging capabilities compared to traditional TDN-based nanodevices. More importantly, simultaneous and precise intracellular imaging of miRNA221 and miRNA222 could effectively distinguish hepatocellular carcinoma cells with different degrees of metastasis from human normal liver cells, providing more precise information for the diagnosis and development of hepatocellular carcinoma.
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http://dx.doi.org/10.1021/acs.analchem.4c05032 | DOI Listing |
Front Mol Biosci
August 2025
Institute of Biological and Chemical Systems - Biological Information Processing, Karlsruhe Institute of Technology, Karlsruhe, Germany.
In this work, we investigate the dependence of the melting temperature of low-valency DNA constructs on the length of non-inert dangling ends, controlling their sequence composition. We compare two computational models to evaluate their effectiveness and limitations in predicting the melting behavior of DNA oligomers (bivalent linkers) and more complex structures (trivalent nanostars), benchmarking the results against experimental spectroscopic data. Our results suggest that the length of non-inert dangling ends has minimal impact on the melting point of the DNA duplex for the duplexes we studied, informing the future design of DNA supramolecular constructs.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Institut de Química Teòrica i Computacional (IQTC), Universitat de Barcelona, C/ Martí i Franquès, 1-11, Barcelona, 08028, Spain.
Inspired by nature, researchers have developed several chemical fuel-driven supramolecular systems aimed at achieving improved kinetic control over their formation and functions. Alongside, DNA-based systems regulated by energy-dissipating mechanisms have been reported. However, the majority of these systems rely on batchwise additions of chemical fuels to closed reactors, resulting in transient non-equilibrium states that differ fundamentally from the sustained and highly adaptable non-equilibrium steady states (NESS) maintained by living systems through continuous energy dissipation.
View Article and Find Full Text PDFJACS Au
August 2025
School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, United Kingdom.
The ability to selectively control DNA conformation using light as an external stimulus offers unique opportunities to control specific DNA sequences in biological settings and to develop nucleotide-based nanodevices. We describe a duplex/G-quadruplex (G4) junction-binding chemotype derived from a cyclic azobenzene core that reversibly photoswitches between and isomers, mediated exclusively by visible light under physiological conditions. We demonstrate the selective binding of the elongated conformation, with over 50-fold higher affinity, toward LTR-III G4 (an important HIV-1 sequence), and show that binding and dissociation from the LTR-III G4 can be controlled reversibly by alternate irradiation with low-intensity blue and green light.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, P. R. China.
Long-range ordered chiral nanoparticle superstructures, formed colloidal self-assembly, exhibit geometrically asymetric structures-such as helices, twisted arrangements, or lattices with low-symmetry space groups-endowed with distinctive chiroptical properties. This review highlights that spherical inorganic nanoparticles typically require chiral templates (, supramolecular polymers, DNA, proteins or liquid crystals) to induce asymmetric spatial organization. In contrast, anisotropic inorganic nanoparticles (, nanorods, tetrahedra, or nanodumbbells) can achieve chiral assembly both with and without templates, the latter driven by interfacial directional forces or geometric curvature matching.
View Article and Find Full Text PDFJ Immunol
August 2025
Department of Immunology, University of Toronto, Toronto, ON, Canada.
C-terminal to LisH (CTLH) E3 ubiquitin ligase complexes regulate a broad range of biological processes and forms separate supramolecular CTLH-MKLN1 and CTLH-WDR26 assemblies possessing distinct substrate specificities. Our previous work revealed that the CTLH complex utilizes the FAM72A substrate adaptor to ubiquitinate and degrade the uracil-DNA glycosylase 2 (UNG2) base excision repair factor. This outcome in B cells permits deoxyuridine mutations catalyzed by activation-induced cytidine deaminase (AID) to persist toward mutational outcomes and drive antibody diversification events.
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