2'-O, 4'-C-Ethylene-bridged nucleic acids (ENA) with nuclease-resistance and high affnity for RNA
Author(s) -
Koji Morita,
Chie Hasegawa,
Masakatsu Kaneko,
Seiichiro Tsutsumi,
Jun Sone,
Tsutomu Ishikawa,
T. IMANISHI,
Masaki Koizumi
Publication year - 2001
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/1.1.241
Subject(s) - nucleic acid , nuclease , oligonucleotide , ethylene , dna , rna , locked nucleic acid , chemistry , stereochemistry , biochemistry , combinatorial chemistry , gene , catalysis
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.
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