Source:http://linkedlifedata.com/resource/pubmed/id/14510495
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-9-26
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pubmed:abstractText |
The translation of HCV starts at the internal ribosomal entry site (IRES) within the 5' untranslated region and IRES is well-conserved in HCV strains. We developed a novel selection strategy using biotinylated oligonucleotide probe and obtained RNA aptamers that bind HCV IRES domain II and domain III-IV, respectively. Selected aptamers specifically bound to target sequence via RNA-RNA interactions. These aptamers inhibited IRES-depend translation in vitro. Especially, 3-07 aptamer, which bound domain IIId, showed strong inhibition. Structure/function relationship of these aptamers was analyzed by mutagenesis, RNase mapping and binding kinetics.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:author | |
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
291-2
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pubmed:dateRevised |
2006-11-30
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pubmed:meshHeading |
pubmed-meshheading:14510495-Base Sequence,
pubmed-meshheading:14510495-DNA, Complementary,
pubmed-meshheading:14510495-Hepacivirus,
pubmed-meshheading:14510495-RNA,
pubmed-meshheading:14510495-Ribosomes,
pubmed-meshheading:14510495-Structure-Activity Relationship,
pubmed-meshheading:14510495-Surface Plasmon Resonance
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pubmed:year |
2003
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pubmed:articleTitle |
Structure-inhibition analysis of RNA aptamers that bind to HCV IRES.
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pubmed:affiliation |
Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology, Higashi, Tsukuba 305-8566, Japan.
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pubmed:publicationType |
Journal Article
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