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Updated: Dec 24, 2025

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
Published on: September 21, 2017
Consecutive 5'- and 3'-amide linkages stabilise antisense oligonucleotides and elicit an efficient RNase H response
Sven Epple1, Cameron Thorpe1, Ysobel R Baker1
1Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA, UK. tom.brown@chem.ox.ac.uk.
Abstract:
Antisense oligonucleotides are now entering the clinic for hard-to-treat diseases. New chemical modifications are urgently required to enhance their drug-like properties. We combine amide coupling with standard oligonucleotide synthesis to assemble backbone chimera gapmers that trigger an efficient RNase H response while improving serum life time and cellular uptake.
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