A highly stabilizing silver(I)-mediated base pair in parallel-stranded DNA

60Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The first parallel-stranded DNA duplex with Hoogsteen base pairing that readily incorporates an Ag+ ion into an internal mispair to form a metal-mediated base pair has been created. Towards this end, the highly stabilizing 6 FP-Ag+-6 FP base pair comprising the artificial nucleobase 6-furylpurine (6 FP) was devised. A combination of temperature-dependent UV spectroscopy, CD spectroscopy, and DFT calculations was used to confirm the formation of this base pair. The nucleobase 6 FP is capable of forming metal-mediated base pairs both by the Watson-Crick edge (i.e. in regular antiparallel-stranded DNA) and by the Hoogsteen edge (i.e. in parallel-stranded DNA), depending on the oligonucleotide sequence and the experimental conditions. The 6 FP-Ag+-6 FP base pair within parallel-stranded DNA is the most strongly stabilizing Ag+-mediated base pair reported to date for any type of nucleic acid, with an increase in melting temperature of almost 15 C upon the binding of one Ag+ ion. I'm stranded: An artificial nucleoside forms Ag+-mediated base pairs both in antiparallel-stranded duplexes with Watson-Crick-type geometry and in parallel-stranded duplexes with Hoogsteen-type geometry. The base pair within the parallel-stranded duplex is significantly more stabilizing and is the most strongly stabilizing Ag+-mediated base pair reported for any type of nucleic acid.

Cite

CITATION STYLE

APA

Sinha, I., Fonsecaguerra, C., & Müller, J. (2015). A highly stabilizing silver(I)-mediated base pair in parallel-stranded DNA. Angewandte Chemie - International Edition, 54(12), 3603–3606. https://doi.org/10.1002/anie.201411931

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free