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dc.contributor.authorCheung, Shane
dc.contributor.authorWu, Dan
dc.contributor.authorDaly, Harrison C.
dc.contributor.authorBusschaert, Nathalie
dc.contributor.authorMorgunova, Marina
dc.contributor.authorSimpson, Jeremy C.
dc.contributor.authorScholz, Dimitri
dc.contributor.authorGale, Philip A.
dc.contributor.authorO'Shea, Donal F.
dc.date.accessioned2019-08-23
dc.date.available2019-08-23
dc.date.issued2018-04-12
dc.identifier.citationCheung, S., Wu, D., Daly, H. C., Busschaert, N., Morgunova, M., Simpson, J. C., … O’Shea, D. F. (2018). Real-Time Recording of the Cellular Effects of the Anion Transporter Prodigiosin. Chem, 4(4), 879–895. https://doi.org/10.1016/j.chempr.2018.02.009en
dc.identifier.urihttp://hdl.handle.net/2123/20952
dc.description.abstractThe unraveling of the cellular effects of anion transporters is key to their potential development as apoptosis-inducing or autophagy-disrupting therapeutics. Here, we conducted a systematic study of the cellular responses to the anion transporter prodigiosin by using a pH on/off responsive near-infrared (NIR)-fluorescent probe in HeLa and LAMP1-GFP-transfected HeLa cell lines. The sequence of localized and global cellular acidity changes and the resulting outcomes induced by the anion transporter were visualized with high temporal and spatial resolution. The results show that prodigiosin causes the pH within the lysosomal lumen to rise, after which a non-organelle-specific increase in acidity of the cytosol takes place, which prompts cells to undergo apoptosis. This was confirmed by the quantification of NIR-emissive lysosomes, the intra-cellular fluorescence intensity, and fluorescence volume over time. This NIR probe overcame the limitations of acridine orange, which to date have severely restricted researchers in this field.en
dc.language.isoenen
dc.publisherCell Pressen
dc.rightsOtheren
dc.subjectapoptosisen
dc.subjectprodigiosinen
dc.subjectimagingen
dc.titleReal-Time Recording of the Cellular Effects of the Anion Transporter Prodigiosinen
dc.typePreprinten
dc.subject.asrc030302en
dc.identifier.doi10.1016/j.chempr.2018.02.009
dc.type.pubtypePre-printen
usyd.facultyFaculty of Science, School of Chemistry


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