Abstract
Locked nucleic acid (LNA) is the term for oligonucleotides that contain one or more nucleotide building blocks in which an extra methylene bridge fixes the ribose moiety either in the C3′-endo (β-D-LNA) or C2′-endo(α-L-LNA) conformation. The β-D-LNA modification results in significant increases in melting temperature of up to several degrees per LNA residue. The α-L-LNA stereoisomer, which also stabilizes duplexes, lends itself to use in triplex-forming oligonucleotides and transcription factor decoys, which have to maintain a B-type (C2′-endo) DNA conformation. LNA oligonucleotides are synthesized in different formats, such as all-LNA, LNA/DNA mixmers, or LNA/DNA gapmers. Essentially, all aspects of antisense technology have profited from LNAdue to its unprecedented affinity, good or even improved mismatch discrimination, low toxicity, and increased metabolic stability. LNA is particularly attractive for in vivo applications that are inaccessible to RNAinterference technology, such as suppression of aberrant splice sites or inhibition of oncogenic microRNAs. Furthermore, the extreme antisense-target duplex stability (formation of persistent steric blocks) conferred by β-D-LNAalso contributes to the capacity to invade stable secondary structures of RNA targets. The in vivo studies reported so far indeed point to LNA as a promising antisense player at the horizon of clinical applications.
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Acknowledgments
We are grateful to Dagmar K. Willkomm for critical reading of the manuscript. Financial support from the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie (R.K. Hartmann), and the Fritz Thyssen Stiftung (A. Grünweller and R.K. Hartmann) is acknowledged. The authors have no conflicts of interest that are directly relevant to the content of this review.
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GrÜnweiler, A., Hartmann, R.K. Locked Nucleic Acid Oligonucleotides. BioDrugs 21, 235–243 (2007). https://doi.org/10.2165/00063030-200721040-00004
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DOI: https://doi.org/10.2165/00063030-200721040-00004