A1 Refereed original research article in a scientific journal

The Impact of Secondary Structure on the Base-Filling of N-Methoxy-1,3-Oxazinane (MOANA) and N-Methoxy-1,3-Oxazolidine Glycol Nucleic Acid (MOGNA) Oligonucleotides




AuthorsAfari, Mark Nana Kwame; Heikinmäki, Ninna; Virta, Pasi; Lönnberg, Tuomas

PublisherJohn Wiley & Sons

Publication year2025

JournalChemBioChem

Journal name in sourceChembiochem : a European journal of chemical biology

Journal acronymChembiochem

Article numbere202400666

Volume26

Issue1

ISSN1439-4227

eISSN1439-7633

DOIhttps://doi.org/10.1002/cbic.202400666

Web address https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cbic.202400666

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/457814437


Abstract
Various single-stranded and hairpin-forming DNA and 2´-O-methyl-RNA oligonucleotides bearing a single (2R,3S)-4-(methoxyamino)butane-1,2,3-triol residue esterified from either O1 and O2 or O1 and O3 were synthesized. Incubation of these oligonucleotides with equimolar mixtures of formylmethyl derivatives of the canonical nucleobases and 2-methylbenzimidazole under mildly acidic conditions revealed base-filling of the modified site to be strongly favored by base stacking of a double-helix, especially an A-type one. In 2´-O-methyl-RNA hairpin oligonucleotides, base-filling of the (2R,3S)-4-(methoxyamino)butane-1,2,3-triol residue with nucleobase aldehydes followed the rules of Watson-Crick base pairing, thymine being the only exception. In single-stranded oligonucleotides or the Hoogsteen strand of triple helices, both the yield and selectivity of base-filling were much more modest.

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Last updated on 2025-27-03 at 13:04