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dc.contributor.authorMao, Hong
dc.contributor.authorDiekmann, Robin
dc.contributor.authorLiang, Hai
dc.contributor.authorCogger, Victoria Carroll
dc.contributor.authorLe Couteur, David George
dc.contributor.authorLockwood, Glen P
dc.contributor.authorHunt, Nick
dc.contributor.authorSchuttpelz, Mark
dc.contributor.authorHuser, Thomas Rolf
dc.contributor.authorChen, Vivien
dc.contributor.authorMcCourt, Peter Anthony
dc.date.accessioned2019-09-23T08:23:45Z
dc.date.available2019-09-23T08:23:45Z
dc.date.issued2019-07-09
dc.description.abstractSingle-molecule localization microscopy (SMLM) provides a powerful toolkit to specifically resolve intracellular structures on the nanometer scale, even approaching resolution classically reserved for electron microscopy (EM). Although instruments for SMLM are technically simple to implement, researchers tend to stick to commercial microscopes for SMLM implementations. Here we report the construction and use of a “custom-built” multi-color channel SMLM system to study liver sinusoidal endothelial cells (LSECs) and platelets, which costs significantly less than a commercial system. This microscope allows the introduction of highly affordable and low-maintenance SMLM hardware and methods to laboratories that, for example, lack access to core facilities housing high-end commercial microscopes for SMLM and EM. Using our custom-built microscope and freely available software from image acquisition to analysis, we image LSECs and platelets with lateral resolution down to about 50 nm. Furthermore, we use this microscope to examine the effect of drugs and toxins on cellular morphology.en_US
dc.description.sponsorshipMcKnight Bequest via the Sydney Medical School Foundation and the Ageing and Alzheimers Institute. The publication charges for this article have been funded by a grant from the publication fund of the University of Tromsø – The Arctic University of Norway.en_US
dc.identifier.citationMao, H., Diekmann, R., Liang, H.P.H., Cogger, V.C., Le Couteur, D.G., Lockwood, G.P., ... McCourt, P.A.G. (2091). Cost-efficient nanoscopy reveals nanoscale architecture of liver cells and platelets. <i>Nanophotonics, 8</i>(7), 1299-1313. https://doi.org/10.1515/nanoph-2019-0066en_US
dc.identifier.cristinIDFRIDAID 1714103
dc.identifier.doihttps://doi.org/10.1515/nanoph-2019-0066
dc.identifier.issn2192-8606
dc.identifier.issn2192-8614
dc.identifier.urihttps://hdl.handle.net/10037/16255
dc.language.isoengen_US
dc.publisherDe Gruyteren_US
dc.relation.ispartofMao, H. (2021). Unraveling nanoscale alterations in liver cell fenestrations - Morphological studies via optical super-resolution microscopy approaches. (Doctoral thesis). <a href=https://hdl.handle.net/10037/20170>https://hdl.handle.net/10037/20170</a>
dc.relation.journalNanophotonics
dc.rights.accessRightsopenAccessen_US
dc.subjectliveren_US
dc.subjectendotheliumen_US
dc.subjectoptical nanoscopyen_US
dc.subjectfenestrationen_US
dc.subjectplateleten_US
dc.subjectVDP::Technology: 500::Nanotechnology: 630en_US
dc.subjectVDP::Teknologi: 500::Nanoteknologi: 630en_US
dc.subjectVDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical molecular biology: 711en_US
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk molekylærbiologi: 711en_US
dc.titleCost-efficient nanoscopy reveals nanoscale architecture of liver cells and plateletsen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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