Quantitative Multiple-Reaction Monitoring Proteomic Analysis of Gβ and Gγ Subunits in C57Bl6/J Brain Synaptosomes
Year: 2017
Type: article
Abstract: Gβγ dimers are one of the essential signaling units of activated G protein-coupled receptors (GPCRs). There are five Gβ and 12 Gγ subunits in humans; numerous studies have demonstrated that different Gβ and Gγ subunits selectively interact to form unique Gβγ dimers, which in turn may target specific receptors and effectors. Perturbation of Gβγ signaling can lead to impaired physiological responses. Moreover, previous targeted multiple-reaction monitoring (MRM) studies of Gβ and Gγ subunits have shown distinct regional and subcellular localization patterns in four brain regions. Nevertheless, no studies have quantified or compared their individual protein levels. In this study, we have developed a quantitative MRM method not only to quantify but also to compare the protein abundance of neuronal Gβ and Gγ subunits. In whole and fractionated crude synaptosomes, we were able to identify the most abundant neuronal Gβ and Gγ subunits and their subcellular localizations. For example, Gβ 1 was mostly localized at the membrane while Gβ 2 was evenly distributed throughout synaptosomal fractions. The protein expression levels and subcellular localizations of Gβ and Gγ subunits may affect the Gβγ dimerization and Gβγ–effector interactions. This study offers not only a new tool for quantifying and comparing Gβ and Gγ subunits but also new insights into the in vivo distribution of Gβ and Gγ subunits, and Gβγ dimer assembly in normal brain function.
Source: Biochemistry
Institutions: Vanderbilt University, University of Michigan
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: Structure and Function of the LPLA2/LCAT Acyltransferase Family, G Protein Structure and Function, G1468576729, Training in Pharmacological Sciences, G3956411418, G4675322906, G5091543464, Michigan Chemistry Biology Interface Training Program, GPCR Regulation of insulin secretion by modulation of the release machinery, G705743126, Optimization of modulators of Gbg-SNARE interaction, Structure, function, and inhibition of G protein-coupled receptor kinases
OpenAlex ID: W2750807579
