Synthesis, duplex-forming properties, and enzymatic resistance of oligonucleotides containing N-acylsulfonamide
Romain Amador1, Carine Baraguey1, Guillaume Clavé1
1Institut des Biomolécules Max Mousseron, Université de Montpellier, CNRS, ENSCM, 1919 route de Mende, 34095 Montpellier, France. guillaume.clave@cnrs.fr.
Abstract:
We report the synthesis of (2-(N-acetylsulfamoyl)ethyl)carbamate (NAC)-linked thymidine dinucleotide via the sulfo-click reaction and its incorporation into DNA oligonucleotides. Thermal denaturation studies indicate modest destabilization at duplex ends (∼1 °C) and stronger effects in the middle (∼7 °C), while the NAC linkage provides complete resistance to nucleases.
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