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Locked nucleic acid: modality, diversity, and drug discovery

Authors :
Henrik Frydenlund Hansen
Marianne R. Møller
Peter Hagedorn
Dennis Jul Hansen
Mads Jensen
Erik Funder
Nanna Albæk
Helle Christiansen
Natalia Papargyri
Sanna L. Diemer
Troels Koch
Robert Persson
Bo Hansen
Source :
Hagedorn, P H, Persson, R, Funder, E D, Albæk, N, Diemer, S L, Hansen, D J, Møller, M R, Papargyri, N, Christiansen, H, Hansen, B R, Hansen, H F, Jensen, M A & Koch, T 2018, ' Locked nucleic acid: modality, diversity, and drug discovery ', Drug Discovery Today, vol. 23, no. 1, pp. 101-114 . https://doi.org/10.1016/j.drudis.2017.09.018
Publication Year :
2018

Abstract

Over the past 20 years, the field of RNA-targeted therapeutics has advanced based on discoveries of modified oligonucleotide chemistries, and an ever-increasing understanding of how to apply cellular assays to identify oligonucleotides with improved pharmacological properties in vivo. Locked nucleic acid (LNA), which exhibits high binding affinity and potency, is widely used for this purpose. Our understanding of RNA biology has also expanded tremendously, resulting in new approaches to engage RNA as a therapeutic target. Recent observations indicate that each oligonucleotide is a unique entity, and small structural differences between oligonucleotides can often lead to substantial differences in their pharmacological properties. Here, we outline new principles for drug discovery exploiting oligonucleotide diversity to identify rare molecules with unique pharmacological properties.

Details

Language :
English
Database :
OpenAIRE
Journal :
Hagedorn, P H, Persson, R, Funder, E D, Albæk, N, Diemer, S L, Hansen, D J, Møller, M R, Papargyri, N, Christiansen, H, Hansen, B R, Hansen, H F, Jensen, M A & Koch, T 2018, ' Locked nucleic acid: modality, diversity, and drug discovery ', Drug Discovery Today, vol. 23, no. 1, pp. 101-114 . https://doi.org/10.1016/j.drudis.2017.09.018
Accession number :
edsair.doi.dedup.....8e87e530133cecf9154e084346d5c3e2
Full Text :
https://doi.org/10.1016/j.drudis.2017.09.018