Issue 15, 2005

RNA duplexes with biphenyl substituents as base replacements are less stable than DNA duplexes

Abstract

Introduction of a hydrophobic biphenyl-C-nucleotide pair into a 11-mer RNA duplex is associated with a net penalty in the free energy of duplex formation of 2.0 kcal mol−1 or 10 °C in Tm, relative to DNA. These differential stabilities are of relevance with respect to the transcriptional and translational aspects of hydrophobic base-pairs.

Graphical abstract: RNA duplexes with biphenyl substituents as base replacements are less stable than DNA duplexes

Supplementary files

Article information

Article type
Communication
Submitted
23 Dec 2004
Accepted
15 Feb 2005
First published
28 Feb 2005

Chem. Commun., 2005, 2023-2025

RNA duplexes with biphenyl substituents as base replacements are less stable than DNA duplexes

C. Brotschi and C. J. Leumann, Chem. Commun., 2005, 2023 DOI: 10.1039/B419278H

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