Two Gα i1 Rate-Modifying Mutations Act in Concert to Allow Receptor-Independent,Steady-State Measurements of RGS Protein Activity

Abstract

RGS proteins are critical modulators of G-protein-coupled receptor (GPCR) signaling given their ability to deactivate Gα subunits via GTPase-accelerating protein (GAP) activity. Their selectivity for specific GPCRs makes them attractive therapeutic targets. However, measuring GAP activity is complicated by slow guanosine diphosphate (GDP) release from Gα and lack of solution phase assays for detecting free GDP in the presence of excess guanosine triphosphate (GTP). To overcome these hurdles, the authors developed a Gα_i1 mutant with increased GDP dissociation and decreased GTP hydrolysis rates, enabling detection of GAP activity using steady-state GTP hydrolysis. Gα_i1(R178M/A326S) GTPase activity was stimulated 6- to 12-fold by RGS proteins known to act on Gα_i subunits and not affected by those unable to act on Gα_i, demonstrating that the Gα/RGS domain interaction selectivity was not altered by mutation. The selectivity and affinity of Gα _i1(R178M/A326S) interaction with RGS proteins was confirmed by molecular binding studies. To enable nonradioactive, homogeneous detection of RGS protein effects on Gα_i1(R178M/A326S), the authors developed a Transcreener ^® fluorescence polarization immunoassay based on a monoclonal antibody that recognizes GDP with greater than 100-fold selectivity over GTP. Combining Gα_i1(R178M/A326S) with a homogeneous, fluorescence-based GDP detection assay provides a facile means to explore the targeting of RGS proteins as a new approach for selective modulation of GPCR signaling.