A convenient method for multicolour labelling of proteins with BODIPY fluorophores via tyrosine residues View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-08-09

AUTHORS

Miffy. H. Y. Cheng, Huguette Savoie, Francesca Bryden, Ross. W. Boyle

ABSTRACT

Fluorescence is an essential imaging modality for labelling and visualising cells and sub-cellular structures. Multicolour labelling is especially challenging due to differences in physicochemical and photophysical behaviour of structurally unrelated fluorophores in the heterogeneous environments found in sub-cellular compartments. Herein, we report the conjugation of three azide-bearing BODIPYs with similar core structures but widely different emission wavelengths (green, red and NIR) to tyrosine residues of a model globular protein (BSA) via a common linking methodology. The resulting BODIPY–BSA conjugates have demonstrated multi-wavelength fluorescence emission for biological applications. Fluorescence imaging was performed in HeLa cells through live cell confocal microscopy imaging, with good intracellular location visualisation observed. More... »

PAGES

1260-1267

Identifiers

URI

http://scigraph.springernature.com/pub.10.1039/c7pp00091j

DOI

http://dx.doi.org/10.1039/c7pp00091j

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1085721820

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/28636039


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