Biochemistry · 1996 · 21 citations · 9 references
Life SciencesBiochemistryMolecular BiologyEnzymologyNucleic Acid BiochemistryNucleic Acid ChemistryDna StructureEnzyme FunctionEnzyme InhibitionEnzyme StabilityNucleic Acid StructureOligonucleotide ChemistryAntisense RnasChemical Modification Of OligonucleotidesDna Polymerase BetaDna Polymerase IMolecular LipophilicityOligonucleotide StabilityOligonucleotide Therapeutics
Boronated oligonucleotides are potential candidates for boron neutron capture therapy, antisense technology, and as tools in molecular biology. The biological properties of dodecathymidylic acids containing one or more 5-(o-carboran-1-yl)-2'-deoxyuridine residues at different locations within the oligonucleotide chain were studied. 5-(o-Carboran-1-yl)-2'-deoxyuridine containing oligonucleotides manifested marked increased lipophilicity and resistance to 3'- or 5'-phosphodiesterases compared to the corresponding unmodified oligomer. They were substrates for T4 polynucleotide kinase and primers for Escherichia coli polymerase I and human immunodeficiency virus type 1 reverse transcriptase but not for human DNA polymerase alpha and beta. They also formed heteroduplexes that were substrates for E. coli RNase H, an essential property for antisense technology. These studies indicate that the carboranyl-containing oligonucleotides have desirable properties that need to be exploited further in the design of novel biopharmaceuticals.
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Sequence‐dependent hydrolysis of RNA using modified oligonucleotide splints and RNase H
Hideo Inoue, Yoji Hayase, Shigenori Iwai et al. · FEBS Letters · 1987 · 260 citations · Full text
Géraldine Fulcrand-El Kattan, Zbigniew J. Leśnikowski, Shijie Yao et al. · Journal of the American Chemical Society · 1994 · 45 citations