Author:
Glatz Richard V.,Leifert Wayne R.,Cooper Tamara H.,Bailey Kelly,Barton Chris S.,Martin A. Scott,Aloia Amanda L.,Bucco Olgatina,Waniganayake Lakshmi,Wei Gang,Raguse Burkhard,Wieczorek Lech,McMurchie Edward J.
Abstract
The ability to express and purify modified recombinant proteins, so they retain their biological function in a cell-free format, has provided a basis for development of molecular biosensors. Here we utilize recombinant G Protein-coupled receptors (GPCRs) and their G proteins for cell-free detection of various binding partners. Fusion peptides were used to improve surface-attachment and fluorescent-labelling capabilities. A novel homogeneous fluorescence resonance energy transfer (FRET)-based assay was developed to detect rearrangements in the G protein heterotrimer. By using this heterotrimeric ‘molecular switch’, we are developing a generic technology such that multiple GPCRs could be assayed for ligand-mediated activation while tethered to surfaces or in solution, with increased throughput compared to current assay platforms.
Cited by
4 articles.
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