Synthesis, biochemical and biological studies on oligonucleotides bearing a lipophilic dimethoxytrityl group

Dimethoxytritylphosphono-oligonucleotide conjugates have been prepared. They are totally resistant to nucleases present in human serum and do not affect cleavage of a complementary oligoribonucleotide by RNase H. Conjugates possessing a phosphate backbone gave better antisense inhibition of expressi...

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Veröffentlicht in:Acta biochimica polonica 1998-01, Vol.45 (1), p.27-32
Hauptverfasser: Misiura, K, Wójcik, M, Krakowiak, A, Koziołkiewicz, M, Pawłowska, Z, Pluskota, E, Cierniewski, C S, Stec, W J
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Sprache:eng
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Zusammenfassung:Dimethoxytritylphosphono-oligonucleotide conjugates have been prepared. They are totally resistant to nucleases present in human serum and do not affect cleavage of a complementary oligoribonucleotide by RNase H. Conjugates possessing a phosphate backbone gave better antisense inhibition of expression of plasminogen activator inhibitor type-1 within endothelial cells as compared with unconjugated oligonucleotides.
ISSN:0001-527X
1734-154X
DOI:10.18388/abp.1998_4315