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Updated: Aug 10, 2026

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
Published on: September 21, 2017
A cyclopentane conformational restraint for a peptide nucleic acid: design, asymmetric synthesis, and improved
Michael C Myers1, Mark A Witschi, Nataliya V Larionova
1Department of Chemistry, Northwestern University, Evanston, Illinois 60208, USA.
Abstract:
[structure: see text] A strategy to restrict the highly flexible backbone conformation of a peptide nucleic acid (PNA) by incorporation of a cyclopentane ring is proposed. An asymmetric synthesis of cyclopentane-modified PNA is reported, and its binding properties were determined. The cyclopentane ring leads to a significant improvement in the binding properties of the resulting PNA to DNA and RNA.
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