Issue 39, 2015

Oligonucleotides containing a ribo-configured cyclohexanyl nucleoside: probing the role of sugar conformation in base pairing selectivity

Abstract

The synthesis and a preliminary evaluation of the pairing properties of ribo-cyclohexanyl nucleic acids (r-CNA) is herein reported. Incorporation of a single r-CNA nucleotide into natural duplexes did not enhance their stability, while a very high pairing selectivity for RNA was found. As deduced by comparative analysis of Tm and NMR data, a relationship between pairing selectivity and conformational preferences of the “sugar” moiety of r-CNA (and more generally of six-membered nucleic acids) was suggested.

Graphical abstract: Oligonucleotides containing a ribo-configured cyclohexanyl nucleoside: probing the role of sugar conformation in base pairing selectivity

Supplementary files

Article information

Article type
Paper
Submitted
15 Jul 2015
Accepted
10 Aug 2015
First published
10 Aug 2015

Org. Biomol. Chem., 2015,13, 10041-10049

Author version available

Oligonucleotides containing a ribo-configured cyclohexanyl nucleoside: probing the role of sugar conformation in base pairing selectivity

C. Paolella, D. D'Alonzo, G. Schepers, A. Van Aerschot, G. Di Fabio, G. Palumbo, P. Herdewijn and A. Guaragna, Org. Biomol. Chem., 2015, 13, 10041 DOI: 10.1039/C5OB01449B

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