| Literature DB >> 10805816 |
C Wahlestedt1, P Salmi, L Good, J Kela, T Johnsson, T Hökfelt, C Broberger, F Porreca, J Lai, K Ren, M Ossipov, A Koshkin, N Jakobsen, J Skouv, H Oerum, M H Jacobsen, J Wengel.
Abstract
Insufficient efficacy and/or specificity of antisense oligonucleotides limit their in vivo usefulness. We demonstrate here that a high-affinity DNA analog, locked nucleic acid (LNA), confers several desired properties to antisense agents. Unlike DNA, LNA/DNA copolymers were not degraded readily in blood serum and cell extracts. However, like DNA, the LNA/DNA copolymers were capable of activating RNase H, an important antisense mechanism of action. In contrast to phosphorothioate-containing oligonucleotides, isosequential LNA analogs did not cause detectable toxic reactions in rat brain. LNA/DNA copolymers exhibited potent antisense activity on assay systems as disparate as a G-protein-coupled receptor in living rat brain and an Escherichia coli reporter gene. LNA-containing oligonucleotides will likely be useful for many antisense applications.Entities:
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Year: 2000 PMID: 10805816 PMCID: PMC25880 DOI: 10.1073/pnas.97.10.5633
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205