Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/108914
DC Field | Value | Language |
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dc.contributor.author | Panarella, Angela | - |
dc.contributor.author | Bexiga, Mariana G. | - |
dc.contributor.author | Galea, George | - |
dc.contributor.author | O' Neill, Elaine D. | - |
dc.contributor.author | Salvati, Anna | - |
dc.contributor.author | Dawson, Kenneth A. | - |
dc.contributor.author | Simpson, Jeremy C. | - |
dc.date.accessioned | 2023-09-25T08:51:38Z | - |
dc.date.available | 2023-09-25T08:51:38Z | - |
dc.date.issued | 2016-07-04 | - |
dc.identifier.issn | 2045-2322 | pt |
dc.identifier.uri | https://hdl.handle.net/10316/108914 | - |
dc.description.abstract | Synthetic nanoparticles are promising tools for imaging and drug delivery; however the molecular details of cellular internalization and trafficking await full characterization. Current knowledge suggests that following endocytosis most nanoparticles pass from endosomes to lysosomes. In order to design effective drug delivery strategies that can use the endocytic pathway, or by-pass lysosomal accumulation, a comprehensive understanding of nanoparticle uptake and trafficking mechanisms is therefore fundamental. Here we describe and apply an RNA interference-based high-content screening microscopy strategy to assess the intracellular trafficking of fluorescently-labeled polystyrene nanoparticles in HeLa cells. We screened a total of 408 genes involved in cytoskeleton and membrane function, revealing roles for myosin VI, Rab33b and OATL1 in this process. This work provides the first systematic large-scale quantitative assessment of the proteins responsible for nanoparticle trafficking in cells, paving the way for subsequent genome-wide studies. | pt |
dc.language.iso | eng | pt |
dc.publisher | Springer Nature | pt |
dc.relation | Principal Investigator (PI) grant (09/IN.1/B2604) from Science Foundation Ireland (SFI) | pt |
dc.relation | grant from the UCD College of Science | pt |
dc.relation | research grant from Science Foundation Ireland (SFI) and is co-funded under the European Regional Development Fund under Grant Number 13/RC/2073. | pt |
dc.rights | openAccess | pt |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt |
dc.subject.mesh | Biological Transport | pt |
dc.subject.mesh | Cytoskeleton | pt |
dc.subject.mesh | Drug Delivery Systems | pt |
dc.subject.mesh | GTPase-Activating Proteins | pt |
dc.subject.mesh | Genome, Human | pt |
dc.subject.mesh | HeLa Cells | pt |
dc.subject.mesh | Humans | pt |
dc.subject.mesh | Lysosome-Associated Membrane Glycoproteins | pt |
dc.subject.mesh | Lysosomes | pt |
dc.subject.mesh | Microscopy | pt |
dc.subject.mesh | Myosin Heavy Chains | pt |
dc.subject.mesh | Nanoparticles | pt |
dc.subject.mesh | Nanotechnology | pt |
dc.subject.mesh | RNA Interference | pt |
dc.subject.mesh | RNA, Small Interfering | pt |
dc.subject.mesh | Vesicular Transport Proteins | pt |
dc.subject.mesh | rab GTP-Binding Proteins | pt |
dc.title | A systematic High-Content Screening microscopy approach reveals key roles for Rab33b, OATL1 and Myo6 in nanoparticle trafficking in HeLa cells | pt |
dc.type | article | - |
degois.publication.firstPage | 28865 | pt |
degois.publication.issue | 1 | pt |
degois.publication.title | Scientific Reports | pt |
dc.peerreviewed | yes | pt |
dc.identifier.doi | 10.1038/srep28865 | pt |
degois.publication.volume | 6 | pt |
dc.date.embargo | 2016-07-04 | * |
uc.date.periodoEmbargo | 0 | pt |
item.fulltext | Com Texto completo | - |
item.grantfulltext | open | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairetype | article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Collections: | I&D CNC - Artigos em Revistas Internacionais |
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File | Description | Size | Format | |
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A-systematic-HighContent-Screening-microscopy-approach-reveals-key-roles-for-Rab33b-OATL1-and-Myo6-in-nanoparticle-trafficking-in-HeLa-cellsScientific-Reports.pdf | 5.8 MB | Adobe PDF | View/Open |
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This item is licensed under a Creative Commons License