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Iron Oxide Nanoparticles Modified with Galloylated DNA for Magnetically Enhanced DNA-Directed Assembly

Title
Iron Oxide Nanoparticles Modified with Galloylated DNA for Magnetically Enhanced DNA-Directed Assembly
Authors
Golla M.; Jeon H.; Albert S.K.; Lee H.; Kang S.; Park M.; Park S.J.
Ewha Authors
박소정
SCOPUS Author ID
박소정scopus
Issue Date
2025
Journal Title
Advanced Science
ISSN
2198-3844JCR Link
Citation
Advanced Science vol. 12, no. 32
Keywords
Dna Conjugation; Iron Oxide Nanoparticle; Magnetic Interaction; Metal-phenol Interaction; Surface Modification; Dna; Ferric Ion; Ferric Oxide; Ferric Compounds; Binding Energy; Iron Oxides; Magnetic Nanoparticles; Metal Nanoparticles; Dna-directed Assembly; Functionalizations; Length Dependence; Magnetic Interactions; One-step Methods; Oxide Nanoparticles; Surface-modification; Surface Treatment; Magnetic Iron Oxide Nanoparticle; Magnetic Iron Oxide Nanoparticles
Publisher
John Wiley and Sons Inc
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
A straightforward, one-step method is presented for DNA functionalization of iron oxide nanoparticles (IONP) using galloylated DNA through multidentate metal-phenol interactions. The DNA-modified IONPs exhibit excellent stability under diverse buffer conditions and display intriguing DNA binding properties, influenced by the superparamagnetic property of IONPs. The DNA denaturation behavior can be categorized into two regimes: the magnetic-dominant regime and the DNA-dominant regime. In the magnetic regime, where IONPs are assembled using relatively short DNA linkers, magnetic and DNA interactions jointly stabilize the assemblies, resulting in an unusually weak length dependence of DNA melting temperature. As the linker length increases, the system transitions into the DNA-dominant regime, where the magnetic effect diminishes, and the assemblies exhibit conventional DNA length-dependence. This study offers a simple and robust approach for DNA functionalization of IONPs, which can be extended to other metal compound nanoparticles, and highlights the potential of utilizing magnetic reinforcement to modulate DNA-based nanoparticle assembly. © 2025 Elsevier B.V., All rights reserved.
DOI
10.1002/advs.202501491
Appears in Collections:
자연과학대학 > 화학·나노과학전공 > Journal papers
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