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BRET-based assay to monitor EGFR transactivation by the ATR reveals G protein-independent activation and ATR-EGFR complexes. | LitMetric

BRET-based assay to monitor EGFR transactivation by the ATR reveals G protein-independent activation and ATR-EGFR complexes.

Biochem Pharmacol

Receptor Biology Group, The School of Biomedical Sciences, Faculty of Medicine, The University of Queensland, St Lucia 4072, Queensland, Australia; Centre for Cardiac and Vasculature Biology, The University of Queensland, St Lucia 4072, Queensland, Australia. Electronic address:

Published: December 2018

AI Article Synopsis

Article Abstract

The type 1 angiotensin II (AngII) receptor (ATR) transactivates the epidermal growth factor receptor (EGFR), which leads to pathological remodeling of heart, blood vessels and kidney. End-point assays are used as surrogates of EGFR activation, however these downstream readouts are not applicable to live cells, in real-time. Herein, we report the use of a bioluminescence resonance energy transfer (BRET)-based assay to assess recruitment of the EGFR adaptor protein, growth factor receptor-bound protein 2 (Grb2), to the EGFR. In a variety of cell lines, both epidermal growth factor (EGF) and AngII stimulated Grb2 recruitment to EGFR. The BRET assay was used to screen a panel of 9 G protein-coupled receptors (GPCRs) and further developed for other EGFR family members (HER2 and HER3); the ATR was able to transactivate HER2, but not HER3. Mechanistically, ATR-mediated ERK1/2 activation was dependent on G and EGFR tyrosine kinase activity, whereas the recruitment of Grb2 to the EGFR was independent of G and only partially dependent on EGFR tyrosine kinase activity. This G independence of EGFR transactivation was confirmed using ATR mutants and in CRISPR cell lines lacking G. EGFR transactivation was also apparently independent of β-arrestins. Finally, we used additional BRET-based assays and confocal microscopy to provide evidence that both AngII- and EGF-stimulation promoted ATR-EGFR heteromerization. In summary, we report an alternative approach to monitoring ATR-EGFR transactivation in live cells, which provides a more direct and proximal view of this process, including the potential for complexes between the ATR and EGFR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491139PMC
http://dx.doi.org/10.1016/j.bcp.2018.10.017DOI Listing

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