| Literature DB >> 12836354 |
K Morita1, C Hasegawa, M Kaneko, S Tsutsumi, J Sone, T Ishikawa, T Imanishi, M Koizumi.
Abstract
Novel nucleosides, 2'-O,4'-C-ethylene nucleosides and their corresponding phosphoramidites, were synthesized as building blocks for antisense oligonucleotides. The 2'-O,4'-C-ethylene linkage of these nucleosides, as well as the linkage of 2'-O,4'-C-methylene nucleosides which are known as bridged nucleic acids (BNA) or locked nucleic acids (LNA), restricts the sugar puckering to the N-conformation. The ethylene-bridged nucleic acids (ENA) showed a high binding affinity for the complementary RNA strand (delta Tm = degrees C/modification) and were approximately 400 and 80 times more nuclease-resistant than natural DNA and BNA/LNA, respectively. These results indicate that ENA have better antisense activity than BNA/LNA.Entities:
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Year: 2001 PMID: 12836354 DOI: 10.1093/nass/1.1.241
Source DB: PubMed Journal: Nucleic Acids Res Suppl