Nucleic Acids Research, 2002, Vol. 30, No. 11 2435-2443
© 2002 Oxford University Press
Design and characterization of decoy oligonucleotides containing locked nucleic acids
Istituto di Chimica Biologica ‘G. Fornaini’, Università degli Studi di Urbino, via Saffi 2, I-61029 Urbino, Italy
Transfection of cis-element double-stranded oligonucleotides, referred to as decoy ODNs, has been reported to be a powerful tool that provides a new class of antigene strategies for gene therapy. However, one of the major limitations of the decoy approach is the rapid degradation of phosphodiester oligonucleotides by intracellular nucleases. To date, several DNA analogs have been employed to overcome this issue, but insufficient efficacy and/or specificity have limited their in vivo usefulness. In this paper we have investigated the use of conformationally restricted nucleotides in the design of decoy molecules for nuclear transcription factor 
B (NF-B). Starting from a synthetic double-stranded oligonucleotide, containing the B consensus binding sequence, we designed a panel of decoy molecules modified to various extents and at various positions with locked nucleic acids (LNAs). Our results indicate that the addition of terminal LNA bases, outside the B sequence, to generate LNA–DNA–LNA co-polymers was sufficient to confer appreciable protection towards nuclease digestion, without interfering with transcription factor binding. Conversely, insertion of LNA substitutions in the context of the B-binding site resulted in further increased stability, but caused a loss of affinity of NF-B for the target sequence. However, our results also indicate that this latter effect was apparently dependent not only on the extent but also on strand positioning of the internal LNA substitutions. This observation is of great importance since it provides evidence for the possibility of tuning DNA–LNA duplexes with internal LNAs into decoy agents with improved features in terms of biological stability and inhibitory effect.
* To whom correspondence should be addressed. Tel: +39 0722 305211; Fax: +39 0722 320188; Email: magnani{at}bib.uniurb.it
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