Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1392282 | European Journal of Medicinal Chemistry | 2015 | 8 Pages |
•A new hairpin ODN quadruplex-based anti-HIV was reported.•These oligomers all possessed high thermal stability.•These oligomers showed anti-HIV activity at low μM concentrations.•These oligomers all possessed elevated resistance in human serum.
We describe the facile syntheses of new modified oligonucleotides based on d(TG3AG) that form bimolecular G-quadruplexes and possess a HEG loop as an inversion of polarity site 3′-3′ or 5′-5′ and aromatic residues conjugated to the 5′-end through phosphodiester bonds. The conjugated hairpin G-quadruplexes exhibited parallel orientation, high thermal stability, elevated resistance in human serum and high or moderate anti-HIV-1 activity with low cytotoxicity. Further, these molecules showed significant binding to HIV envelope glycoproteins gp120, gp41 and HSA, as revealed by SPR assays. As a result, these conjugated hairpins represent the first active anti-HIV-1 bimolecular G-quadruplexes based on the d(TG3AG) sequence.
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