Literature DB >> 27164033

Cell-free translation and purification of Arabidopsis thaliana regulator of G signaling 1 protein.

Bo Li1, Shin-Ichi Makino2, Emily T Beebe2, Daisuke Urano1, David J Aceti2, Tina M Misenheimer2, Jonathan Peters1, Brian G Fox2, Alan M Jones3.   

Abstract

Arabidopsis thaliana Regulator of G protein Signalling 1 (AtRGS1) is a protein with a predicted N-terminal 7-transmembrane (7TM) domain and a C-terminal cytosolic RGS1 box domain. The RGS1 box domain exerts GTPase activation (GAP) activity on Gα (AtGPA1), a component of heterotrimeric G protein signaling in plants. AtRGS1 may perceive an exogenous agonist to regulate the steady-state levels of the active form of AtGPA1. It is uncertain if the full-length AtRGS1 protein exerts any atypical effects on Gα, nor has it been established exactly how AtRGS1 contributes to perception of an extracellular signal and transmits this response to a G-protein dependent signaling cascade. Further studies on full-length AtRGS1 have been inhibited due to the extreme low abundance of the endogenous AtRGS1 protein in plants and lack of a suitable heterologous system to express AtRGS1. Here, we describe methods to produce full-length AtRGS1 by cell-free synthesis into unilamellar liposomes and nanodiscs. The cell-free synthesized AtRGS1 exhibits GTPase activating activity on Gα and can be purified to a level suitable for biochemical analyses.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  7-Transmembrane protein; Arabidopsis regulator of G signaling protein 1 (AtRGS1); In vitro translation; Membrane scaffold protein 1D1; Nanodiscs

Mesh:

Substances:

Year:  2016        PMID: 27164033      PMCID: PMC5594927          DOI: 10.1016/j.pep.2016.04.016

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


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