A Conserved Protein Interaction Interface on the Type 5 G Protein beta Subunit Controls Proteolytic Stability and Activity of R7 Family Regulator of G Protein Signaling Proteins

作者：Porter Morwenna Y; Xie Keqiang; Pozharski Edwin; Koelle Michael R^*; Martemyanov Kirill A

来源：Journal of Biological Chemistry, 2010, 285(52): 41100-41112.

DOI：10.1074/jbc.M110.163600

Regulators of G protein signaling (RGS) proteins of the R7 subfamily limit signaling by neurotransmitters in the brain and by light in the retina. They form obligate complexes with the G beta 5 protein that are subject to proteolysis to control their abundance and alter signaling. The mechanisms that regulate this proteolysis, however, remain unclear. We used genetic screens to find mutations in G beta 5 that selectively destabilize one of the R7 RGS proteins in Caenorhabditis elegans. These mutations cluster at the binding interface between G beta 5 and the N terminus of R7 RGS proteins. Equivalent mutations within mammalian G beta 5 allowed the interface to still bind the N-terminal DEP domain of R7 RGS proteins, and mutant G beta 5-R7 RGS complexes initially formed in cells but were then rapidly degraded by proteolysis. Molecular dynamics simulations suggest the mutations weaken the G beta 5-DEP interface, thus promoting dynamic opening of the complex to expose determinants of proteolysis known to exist on the DEP domain. We propose that conformational rearrangements at the G beta 5-DEP interface are key to controlling the stability of R7 RGS protein complexes.

• 出版日期2010-12-24