Synthesis and characterization of dumbbell oligonucleotides containing
loops of phosphodiester, two/ three trimethylene, C3 moieties in each
loop and phosphorothioate linkages is described. Incubation of dumbbell
oligonucleotides containing loops of phosphorothioate with S-1 did not
result in significant cleavage. Binding of dumbbell oligonucleotides to
MoMuL Virus reverse transcriptase was evaluated by PAGE band mobility
shift assays. Dissociation constants evaluated using PAGE band mobility
shift assays were of the order of 10-7. Investigation of inhibition of
RNase H activity of reverse transcriptase showed that the dumbbell
oligonucleotides containing loops of phosphorothioate are better
inhibitor of the retroviral RNase H activity than the dumbbell
oligonucleotides containing loops of phosphodiester, two/ three
trimethylene, C3 moieties in each loop. Our studies demonstrated that
the oligonucleotides containing loops of phosphorothioate displays an
IC50 of 18- 25 nM in its inhibition on the reverse transcriptase RNase H
activity, a magnitude lower than that of first nucleotide reverse
transcriptase of HIV-1, tenofovir, introduced by Gilead Science in the
market.