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Article: High-resolution visualisation of antisense oligonucleotide release from polymers in cells

TitleHigh-resolution visualisation of antisense oligonucleotide release from polymers in cells
Authors
Issue Date28-Aug-2024
PublisherRoyal Society of Chemistry
Citation
Chemical Science, 2024, v. 15, n. 38, p. 15690-15697 How to Cite?
Abstract

Antisense oligonucleotides (ASOs) are a well-established therapeutic modality based on RNA interference, but low cellular uptake, limited ability to direct ASO trafficking, and a range of intracellular barriers to successful activity compromise both gene silencing outcomes and clinical translations. Herein, we demonstrate that polymers can increase ASO internalisation via intracellular trafficking pathways that are distinct from lipid-based delivery reagents. For the first time, we spatially define internalisation and dissociation stages in the polymer-mediated cytosolic delivery of ASOs using Nanoscale Secondary Ion Mass Spectrometry (NanoSIMS), which enables visualisation of ASO localisation at the organelle level. We find that polymer-ASO complexes are imported into cells, from which free ASO enters the cytosol following complex dissociation. This information enables a better understanding of the intracellular trafficking pathways of nucleic acid therapeutics and may be exploited for therapeutic delivery to enhance the effectiveness of nucleic acid therapeutics in the future.


Persistent Identifierhttp://hdl.handle.net/10722/365981
ISSN
2023 Impact Factor: 7.6
2023 SCImago Journal Rankings: 2.333

 

DC FieldValueLanguage
dc.contributor.authorKing, Jessica J-
dc.contributor.authorChen, Kai-
dc.contributor.authorEvans, Cameron W-
dc.contributor.authorNorret, Marck-
dc.contributor.authorAlmasri, Ruba-
dc.contributor.authorPavlos, Nathan J-
dc.contributor.authorHui, Henry YL-
dc.contributor.authorLin, Qiongxiang-
dc.contributor.authorBhatt, Uditi-
dc.contributor.authorYoung, Stephen G-
dc.contributor.authorSmith, Nicole M-
dc.contributor.authorNikan, Mehran-
dc.contributor.authorPrestidge, Clive A-
dc.contributor.authorJiang, Haibo-
dc.contributor.authorIyer, K Swaminathan-
dc.date.accessioned2025-11-14T02:40:47Z-
dc.date.available2025-11-14T02:40:47Z-
dc.date.issued2024-08-28-
dc.identifier.citationChemical Science, 2024, v. 15, n. 38, p. 15690-15697-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/10722/365981-
dc.description.abstract<p>Antisense oligonucleotides (ASOs) are a well-established therapeutic modality based on RNA interference, but low cellular uptake, limited ability to direct ASO trafficking, and a range of intracellular barriers to successful activity compromise both gene silencing outcomes and clinical translations. Herein, we demonstrate that polymers can increase ASO internalisation via intracellular trafficking pathways that are distinct from lipid-based delivery reagents. For the first time, we spatially define internalisation and dissociation stages in the polymer-mediated cytosolic delivery of ASOs using Nanoscale Secondary Ion Mass Spectrometry (NanoSIMS), which enables visualisation of ASO localisation at the organelle level. We find that polymer-ASO complexes are imported into cells, from which free ASO enters the cytosol following complex dissociation. This information enables a better understanding of the intracellular trafficking pathways of nucleic acid therapeutics and may be exploited for therapeutic delivery to enhance the effectiveness of nucleic acid therapeutics in the future.</p>-
dc.languageeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.ispartofChemical Science-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleHigh-resolution visualisation of antisense oligonucleotide release from polymers in cells-
dc.typeArticle-
dc.identifier.doi10.1039/d3sc06773d-
dc.identifier.scopuseid_2-s2.0-85203505270-
dc.identifier.volume15-
dc.identifier.issue38-
dc.identifier.spage15690-
dc.identifier.epage15697-
dc.identifier.eissn2041-6539-
dc.identifier.issnl2041-6520-

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