The Journal of Organic Chemistry · 2018 · 12 citations · 32 references
PharmacyChemical BiologyMolecular BiologyBioorthogonal ChemistryGene ExpressionMolecular PharmacologyNucleic Acid SynthesisOligonucleotide ChemistryRibonucleic Acid (Rna) ChemistryRna EngineeringRna InterferenceRna ModificationChemical Modification Of OligonucleotidesConjugated OligonucleotidesLuciferase Reporter AssaysLuciferase ReportersOligonucleotide Backbone ModificationsOligonucleotide SynthesisSmall Interfering Rna ChemistrySolid-phase Oligonucleotide Synthesis
Cross-linkable 7-deaza-6-vinylguanosine (ADVP) and 7-propynyl-7-deaza-6-vinylguanosine (ADpVP) derivatives were synthesized and successfully incorporated into 2'-OMe-RNA oligonucleotides by solid-phase oligonucleotide synthesis. Analysis of their cross-link properties revealed that the 7-propynyl substituent on ADpVP induces a significant enhancement of the cross-link kinetics of the proximal 6-vinyl group to the complementary uracil base in the target RNA compared to that of ADVP. In addition, the 2'-OMe-RNA oligonucleotide containing ADpVP exhibited a higher antisense effect on luciferase production in the cell lysate than that of ADVP. These results suggested that the 7-substituted 7-deaza-6-vinylguanosine derivatives can be used as potent cross-linkers to target mRNA inside of cells.
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