Quantification of functionalised gold nanoparticle-targeted knockdown of gene expression in HeLa cells

DC FieldValueLanguage
dc.contributor.authorJiwaji, Meesbah-
dc.contributor.authorSandison, Mairi E.-
dc.contributor.authorReboud, Julien-
dc.contributor.authorKolch, Walter-
dc.contributor.authoret al.-
dc.date.accessioned2019-04-03T09:36:42Z-
dc.date.available2019-04-03T09:36:42Z-
dc.date.copyright2014 the Authorsen_US
dc.date.issued2014-06-13-
dc.identifier.citationPLoS Oneen_US
dc.identifier.urihttp://hdl.handle.net/10197/9787-
dc.description.abstractINTRODUCTION: Gene therapy continues to grow as an important area of research, primarily because of its potential in the treatment of disease. One significant area where there is a need for better understanding is in improving the efficiency of oligonucleotide delivery to the cell and indeed, following delivery, the characterization of the effects on the cell. METHODS: In this report, we compare different transfection reagents as delivery vehicles for gold nanoparticles functionalized with DNA oligonucleotides, and quantify their relative transfection efficiencies. The inhibitory properties of small interfering RNA (siRNA), single-stranded RNA (ssRNA) and single-stranded DNA (ssDNA) sequences targeted to human metallothionein hMT-IIa are also quantified in HeLa cells. Techniques used in this study include fluorescence and confocal microscopy, qPCR and Western analysis. FINDINGS: We show that the use of transfection reagents does significantly increase nanoparticle transfection efficiencies. Furthermore, siRNA, ssRNA and ssDNA sequences all have comparable inhibitory properties to ssDNA sequences immobilized onto gold nanoparticles. We also show that functionalized gold nanoparticles can co-localize with autophagosomes and illustrate other factors that can affect data collection and interpretation when performing studies with functionalized nanoparticles. CONCLUSIONS: The desired outcome for biological knockdown studies is the efficient reduction of a specific target; which we demonstrate by using ssDNA inhibitory sequences targeted to human metallothionein IIa gene transcripts that result in the knockdown of both the mRNA transcript and the target protein.en_US
dc.description.sponsorshipScience Foundation Irelanden_US
dc.language.isoenen_US
dc.publisherPublic Library of Scienceen_US
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.subjectHeLa cellsen_US
dc.subjectGene therapyen_US
dc.subjectOligonucleotide deliveryen_US
dc.subjectGold nanoparticlesen_US
dc.subjectOligonucleotidesen_US
dc.subjectGene expressionen_US
dc.subjectConfocal microscopyen_US
dc.subjectFluorescence microscopyen_US
dc.titleQuantification of functionalised gold nanoparticle-targeted knockdown of gene expression in HeLa cellsen_US
dc.typeJournal Articleen_US
dc.statusPeer revieweden_US
dc.identifier.volume9en_US
dc.identifier.issue6en_US
dc.identifier.doi10.1371/journal.pone.0099458-
dc.neeo.contributorJiwaji|Meesbah|aut|-
dc.neeo.contributorSandison|Mairi E.|aut|-
dc.neeo.contributorReboud|Julien|aut|-
dc.neeo.contributorKolch|Walter|aut|-
dc.neeo.contributoret al.||aut|-
dc.description.othersponsorshipEngineering and Physical Sciences Research Council (UK)en_US
dc.date.updated2017-12-13-
dc.identifier.grantidEP/E032745/1-
dc.identifier.grantid06/CE/B1129-
item.fulltextWith Fulltext-
item.grantfulltextopen-
Appears in Collections:Conway Institute Research Collection
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