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Newlands Press, Future Medicinal Chemistry, 13(7), p. 1733-1749, 2015

DOI: 10.4155/fmc.15.90

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Polyamine–oligonucleotide conjugates: a promising direction for nucleic acid tools and therapeutics

Journal article published in 2015 by Mirjam Menzi, Helen L. Lightfoot, Jonathan Hall
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Chemical modification and/or the conjugation of small functional molecules to oligonucleotides have significantly improved their biological and biophysical properties, addressing issues such as poor cell penetration, stability to nucleases and low affinity for their targets. Here, the authors review the literature reporting on the biophysical, biochemical and biological properties of one particular class of modification – polyamine–oligonucleotide conjugates. Naturally derived and synthetic polyamines have been grafted onto a variety of oligonucleotide formats, including antisense oligonucleotides and siRNAs. In many cases this has had beneficial effects on their properties such as target hybridization, nuclease resistance, cellular uptake and activity. Polyamine–oligonucleotide conjugation, therefore, represents a promising direction for the further development of oligonucleotide-based therapeutics and tools.