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dc.contributor.authorWang, Z
dc.contributor.authorWang, H
dc.contributor.authorLin, S
dc.contributor.authorLabib, Mahmoud
dc.contributor.authorAhmed, S
dc.contributor.authorDas, J
dc.contributor.authorAngers, S
dc.contributor.authorSargent, EH
dc.contributor.authorKelley, SO
dc.date.accessioned2023-08-01T10:20:01Z
dc.date.available2023-08-01T10:20:01Z
dc.date.issued2023-07-12
dc.identifier.issn1530-6992
dc.identifier.issn1530-6992
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/21117
dc.description.abstract

Nanoneedles are a useful tool for delivering exogenous biomolecules to cells. Although therapeutic applications have been explored, the mechanism regarding how cells interact with nanoneedles remains poorly studied. Here, we present a new approach for the generation of nanoneedles, validated their usefulness in cargo delivery, and studied the underlying genetic modulators during delivery. We fabricated arrays of nanoneedles based on electrodeposition and quantified its efficacy of delivery using fluorescently labeled proteins and siRNAs. Notably, we revealed that our nanoneedles caused the disruption of cell membranes, enhanced the expression of cell–cell junction proteins, and downregulated the expression of transcriptional factors of NFκB pathways. This perturbation trapped most of the cells in G2 phase, in which the cells have the highest endocytosis activities. Taken together, this system provides a new model for the study of interactions between cells and high-aspect-ratio materials.

dc.format.extent5877-5885
dc.format.mediumPrint-Electronic
dc.languageen
dc.publisherAmerican Chemical Society
dc.subjectElectrodeposition
dc.subjectnanostructure
dc.subjectintracellular delivery
dc.subjectmechanobiology
dc.subjectcell cycle
dc.titleEfficient Delivery of Biological Cargos into Primary Cells by Electrodeposited Nanoneedles via Cell-Cycle-Dependent Endocytosis
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000971993400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue13
plymouth.volume23
plymouth.publication-statusPublished
plymouth.journalNano Letters
dc.identifier.doi10.1021/acs.nanolett.2c05083
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
dc.publisher.placeUnited States
dcterms.dateAccepted2023-03-25
dc.date.updated2023-08-01T10:19:39Z
dc.rights.embargodate2024-4-10
dc.identifier.eissn1530-6992
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.1021/acs.nanolett.2c05083


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