C5-Propynyl modified 2′-fluoroarabinonucleic acids form stable duplexes with RNA that are RNase H competent

Abstract

The clinical success of the antisense approach for the treatment of genetic disorders is indisputably the result of chemical modifications along the oligonucleotide (ON) scaffold, which impart desirable properties including high RNA affinity, nuclease stability and improved drug delivery. While effective, many modifications are not capable of eliciting an RNase H response limiting their application in antisense systems. To contribute to the structural design and inventory of nucleoside analogues with favorable antisense properties, herein we describe the synthesis of C5-propynyl-2′-fluoroarabinonucleic acids (FANA^P). Incorporation of individual and multiple uridine (FaraU^P) and cytidine (FaraC^P) inserts into ONs revealed, both stabilized duplexes formed with RNA. In contrast, these modifications demonstrated a negligible (FaraU^P) or reduced (FaraC^P) effect on DNA binding. Moreover, modified ONs containing these analogues supported E. coli RNase H cleavage of RNA with an altered cleavage pattern observed relative to controls. Moreover, a 2′-O-methoxyethyl (2′-O-MOE) gapmer with a FANA^P core was able to elicit RNA cleavage at an increased rate compared to C5-propynyl-arabinonucleic acids (ANA^P). Enzymatic hydrolysis of these gapmers was assessed with nuclease S1 digestion and revealed greater stability of ANA^P compared to FANA^P. These results suggest C5-propynyl ANA/FANA modifications demonstrate promising potential for the design of therapeutic ONs.