Show simple item record

FieldValueLanguage
dc.contributor.authorTrinh, Natalie
dc.contributor.authorJolliffe, Katrina A
dc.contributor.authorNew, Elizabeth J
dc.date.accessioned2021-12-03T04:29:23Z
dc.date.available2021-12-03T04:29:23Z
dc.date.issued2020en
dc.identifier.urihttps://hdl.handle.net/2123/27125
dc.description.abstractA key current challenge in biological research is the elucidation of the roles that chemicals and chemical reactions play in cellular function and dysfunction. Of the available cellular imaging techniques, fluorescence imaging offers a balance between sensitivity and resolution, enabling the cost-effective and rapid visualisation of model biological systems. Importantly, the use of responsive fluorescent probes in conjunction with ever-advancing microscopy and flow cytometry techniques enables the visualisation, with high spatiotemporal resolution, of both specific chemical species and chemical reactions in living cells. Ideal responsive fluorescent probes are those that contain a fluorophore tethered to both a sensing unit, to ensure selectivity of response, and a targeting group, to control the sub-cellular localisation of the probe. To date, probes that are both targeted and selective are relatively rare and most localised probes are discovered serendipitously rather than by design. A challenge in this field is therefore the identification of suitable fluorophore scaffolds that can be readily attached to both sensing and targeting groups. Here we review current strategies for dual-functionalisation of fluorophores, highlighting key examples of targeted, responsive probes.en
dc.language.isoenen
dc.publisherWileyen
dc.relation.ispartofAngewandte Chemie International Editionen
dc.rightsOtheren
dc.titleDual-functionalisation of fluorophores for the preparation of targeted and selective probesen
dc.typeArticleen
dc.subject.asrc0302 Inorganic Chemistryen
dc.subject.asrc0304 Medicinal and Biomolecular Chemistryen
dc.subject.asrc0305 Organic Chemistryen
dc.identifier.doi10.1002/anie.202007673
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcDP180101353
dc.rights.other"This is the peer reviewed version of the following article: N. Trinh, K. A. Jolliffe, E. J. New, Angew. Chem. Int. Ed. 2020, 59, 20290.. which has been published in final form at https://onlinelibrary. https://doi.org/10.1002/anie.202007673. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited."en
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.citation.volume59en
usyd.citation.issue46en
usyd.citation.spage20290en
usyd.citation.epage20301en
workflow.metadata.onlyNoen


Show simple item record

Associated file/s

Associated collections

Show simple item record

There are no previous versions of the item available.