Silver cations(Ag^(+))exhibit site-specific coordination with the natural nucleobases,which can be exploited within DNA nanostructures.Understanding the thermodynamics of formation and organization of DNA complexes fo...Silver cations(Ag^(+))exhibit site-specific coordination with the natural nucleobases,which can be exploited within DNA nanostructures.Understanding the thermodynamics of formation and organization of DNA complexes formed by these interactions is essential for rationally designing Ag^(+)-mediated DNA nanostructures.In this study,we use temperature controlled circular dichroism(CD)spectroscopy,isothermal titration calorimetry(ITC),Förster resonance energy transfer(FRET),and cryogenic-transmission electron microscopy(cryo-TEM)to investigate the formation stoichiometry and resulting morphology of Ag^(+)-mediated duplexes of oligo-dA and oligo-dT homonucleotide strands.CD shows that duplex formation occurs at room temperature and is sensitive to solution phase conditions.ITC reveals that 0.5[Ag^(+)]/[base]is required to form thermodynamically stable dA–Ag^(+)–dT structures with one Ag^(+)per base pair.FRET experiments show that dA–Ag^(+)–dT duplexes maintain anti-parallel strand orientation,even with excess Ag^(+),and cryo-TEM shows that dA–Ag^(+)–dT duplexes adopt morphologies similar to WCF duplexes.Despite these similarities,dA–Ag^(+)–dT duplexes exhibit significantly greater thermal stability compared to their WCF counterparts.These findings provide new insights into dA–Ag^(+)–dT duplex formation and structure that are essential for the development of programmable Ag^(+)–DNA nanostructures.展开更多
基金supported by AFOSR FA9550-21-1-0163 and AFOSR DURIP FA9550-22-1-0206supported in part by the National Science Foundation Materials Research Science and Engineering Center program through the UC Irvine Center for Complex and Active Materials(DMR-2011967).
文摘Silver cations(Ag^(+))exhibit site-specific coordination with the natural nucleobases,which can be exploited within DNA nanostructures.Understanding the thermodynamics of formation and organization of DNA complexes formed by these interactions is essential for rationally designing Ag^(+)-mediated DNA nanostructures.In this study,we use temperature controlled circular dichroism(CD)spectroscopy,isothermal titration calorimetry(ITC),Förster resonance energy transfer(FRET),and cryogenic-transmission electron microscopy(cryo-TEM)to investigate the formation stoichiometry and resulting morphology of Ag^(+)-mediated duplexes of oligo-dA and oligo-dT homonucleotide strands.CD shows that duplex formation occurs at room temperature and is sensitive to solution phase conditions.ITC reveals that 0.5[Ag^(+)]/[base]is required to form thermodynamically stable dA–Ag^(+)–dT structures with one Ag^(+)per base pair.FRET experiments show that dA–Ag^(+)–dT duplexes maintain anti-parallel strand orientation,even with excess Ag^(+),and cryo-TEM shows that dA–Ag^(+)–dT duplexes adopt morphologies similar to WCF duplexes.Despite these similarities,dA–Ag^(+)–dT duplexes exhibit significantly greater thermal stability compared to their WCF counterparts.These findings provide new insights into dA–Ag^(+)–dT duplex formation and structure that are essential for the development of programmable Ag^(+)–DNA nanostructures.
