Abstract
Aptamers targeting NF-kappaB containing thymidine 3'-O-phosphorodithioates in selected positions of an oligonucleotide duplex were synthesized. Binding affinities to NF-kappaB varied with the number and positions of the dithioate backbone substitutions. One of the aptamers showed specific binding to a single NF-kappaB dimer in cell culture extracts.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Base Sequence
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Magnetic Resonance Spectroscopy
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NF-kappa B / metabolism*
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Oligonucleotides / chemical synthesis*
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Oligonucleotides / chemistry
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Oligonucleotides / metabolism
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Organothiophosphorus Compounds / analysis*
Substances
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NF-kappa B
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Oligonucleotides
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Organothiophosphorus Compounds