Unveiling the solution structure of a DNA duplex with continuous silver-modified Watson-Crick base pairs
Metadatos
Mostrar el registro completo del ítemAutor
Javornik, Uroš; Pérez Romero, Antonio; López-Chamorro, Carmen; Smith, Rachelle M.; Dobado Jiménez, José Antonio; Palacios, Óscar; Bera, Mrinal K.; Nyman, May; Plavec, Janez; Galindo, Miguel A.Editorial
Nature Research
Fecha
2024-09-05Referencia bibliográfica
Javornik, U. et. al. Nat Commun 15, 7763 (2024). [https://doi.org/10.1038/s41467-024-51876-8]
Patrocinador
Spanish MINECO (project PID2020-120186RBI00); Spanish MICIU (Salvador Madariaga Program, Ref. PRX19/00290); Junta de Andalucia (project P20_00702); Slovenian Research Agency (grants P1-0242 and J1-1704); Spanish Ministerio de Ciencia e Innovación (PID2022-138479NB-I00); “Grup de Recerca de la Generalitat de Catalunya” (Ref. 2021 SGR 00668); CERIC-ERIC Consortium Project 20172040 and 20222132; National Science Foundation, under grant number NSF/CHE-1834750; DOE Office of Science by Argonne National Laboratory (ANL) under Contract No. DE-AC02-06CH11357Resumen
The challenge of transforming organized DNA structures into their metallized
counterparts persists in the scientific field. In this context, utilizing DNA
moleculesmodified with 7-deazapurine, provides a transformative solution. In
this study, we present the solution structure of a DNA duplex that can be
transformed into its metallized equivalent while retaining the natural base
pairing arrangement through the creation of silver-modified Watson-Crick
base pairs. Unlike previously documented X-ray structures, our research
demonstrates the feasibility of preserving the intrinsic DNA self-assembly
while incorporating AgI into the double helix, illustrating that the binding of
silver does not disrupt the canonical base-pairing organization. Moreover, in
our case, the uninterrupted AgI chain deviates from forming conventional
straight linear chains; instead, it adheres to a helical arrangement dictated by
the underlying DNA structure. This research challenges conventional
assumptions and opens the door to precisely design structures based on the
organization of highly stable Ag-DNA assemblies.