Automated screening of AURKA activity based on a genetically encoded FRET biosensor using fluorescence lifetime imaging microscopy.


Journal

Methods and applications in fluorescence
ISSN: 2050-6120
Titre abrégé: Methods Appl Fluoresc
Pays: England
ID NLM: 101608648

Informations de publication

Date de publication:
20 Feb 2020
Historique:
pubmed: 8 2 2020
medline: 8 10 2020
entrez: 8 2 2020
Statut: epublish

Résumé

Fluorescence Lifetime Imaging Microscopy (FLIM) is a robust tool to measure Förster Resonance Energy Transfer (FRET) between two fluorescent proteins, mainly when using genetically-encoded FRET biosensors. It is then possible to monitor biological processes such as kinase activity with a good spatiotemporal resolution and accuracy. Therefore, it is of interest to improve this methodology for future high content screening purposes. We here implement a time-gated FLIM microscope that can image and quantify fluorescence lifetime with a higher speed than conventional techniques such as Time-Correlated Single Photon Counting (TCSPC). We then improve our system to perform automatic screen analysis in a 96-well plate format. Moreover, we use a FRET biosensor of AURKA activity, a mitotic kinase involved in several epithelial cancers. Our results show that our system is suitable to measure FRET within our biosensor paving the way to the screening of novel compounds, potentially allowing to find new inhibitors of AURKA activity.

Identifiants

pubmed: 32032967
doi: 10.1088/2050-6120/ab73f5
doi:

Substances chimiques

AURKA protein, human EC 2.7.11.1
Aurora Kinase A EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

024006

Auteurs

Florian Sizaire (F)

Univ Rennes, CNRS, IGDR (Genetics and Development Institute of Rennes), UMR 6290, F-35000 Rennes, France.

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Classifications MeSH