High affinity RNA targeting by oligonucleotides displaying aromatic stacking and amino groups in the major groove. Comparison of triazoles and phenylsubstituents

Pawan Kumar, Mick Hornum, Lise Junker Nielsen, Gerald Enderlin, Nicolai Krog Andersen, Christophe Len, Gwénaëlle Hervé, Guillaume Sartori , Poul Nielsen

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Three 5-modified 2'-deoxyuridine nucleosides were synthesized and incorporated into oligonucleotides and compared with the previously published 5-(1-phenyl-1,2,3-triazol-4-yl)-2'-deoxyuridine monomer W. The introduction of an aminomethyl group on the phenyl group led to monomer X, which was found to thermally stabilize a 9-mer DNA:RNA duplex, presumably through the partial neutralization of the negative charge of the backbone. By also taking advantage of the stacking interactions in the major groove of two or more of the monomer X, an extremely high thermal stability was obtained. A regioisomer of the phenyltriazole substituent, that is the 5-(4-phenyl-1,2,3-triazol-1-yl)-2'-deoxyuridine monomer Y, was found to destabilize the DNA:RNA duplex significantly, but stacking in the major groove compensated for this when two to four monomers were incorporated consecutively. Finally, the 5-phenyl-2'-deoxyuridine monomer Z was incorporated for comparison, and it was found to give a more neutral influence on duplex stability indicating less efficient stacking interactions. The duplexes were investigated by CD spectroscopy and MD simulations.
Original languageEnglish
JournalJournal of Organic Chemistry
Volume79
Issue number7
Pages (from-to)2854-2863
Number of pages10
ISSN0022-3263
DOIs
Publication statusPublished - 2014

Cite this