Luciferase Complementation Based-Detection of G-Protein-Coupled Receptor Activity
Author(s) -
Hideaki Yano,
Ning Cai,
Jonathan A. Javitch,
Sergi Ferré
Publication year - 2018
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/btn-2018-0039
Subject(s) - g protein coupled receptor , luciferase , computational biology , complementation , protein fragment complementation assay , fusion protein , biology , protein–protein interaction , drug discovery , receptor , bioinformatics , transfection , microbiology and biotechnology , recombinant dna , biochemistry , gene , phenotype
Protein complementation assays (PCA) are used as pharmacological tools, enabling a wide array of applications, ranging from studies of protein–protein interactions to second messenger effects. Methods to detect activities of G protein-coupled receptors (GPCRs) have particular relevance for drug screening. Recent development of an engineered luciferase NanoLuc created the possibility of generating a novel PCA, which in turn could open a new avenue for developing drug screening assays. Here we identified a novel split position for NanoLuc and demonstrated its use in a series of fusion constructs to detect the activity of GPCRs. The split construct can be applied to a variety of pharmacological screening systems.
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