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Cell-free translation and purification of Arabidopsis thaliana regulator of G signaling 1 protein.
Li, Bo; Makino, Shin-Ichi; Beebe, Emily T; Urano, Daisuke; Aceti, David J; Misenheimer, Tina M; Peters, Jonathan; Fox, Brian G; Jones, Alan M.
Afiliação
  • Li B; Department of Biology, University of North Carolina at Chapel Hill, United States.
  • Makino SI; Transmembrane Protein Center, University of Wisconsin-Madison, United States.
  • Beebe ET; Transmembrane Protein Center, University of Wisconsin-Madison, United States.
  • Urano D; Department of Biology, University of North Carolina at Chapel Hill, United States.
  • Aceti DJ; Transmembrane Protein Center, University of Wisconsin-Madison, United States.
  • Misenheimer TM; Transmembrane Protein Center, University of Wisconsin-Madison, United States.
  • Peters J; Department of Biology, University of North Carolina at Chapel Hill, United States.
  • Fox BG; Transmembrane Protein Center, University of Wisconsin-Madison, United States.
  • Jones AM; Department of Biology, University of North Carolina at Chapel Hill, United States; Department of Pharmacology, University of North Carolina at Chapel Hill, United States. Electronic address: alan_jones@unc.edu.
Protein Expr Purif ; 126: 33-41, 2016 10.
Article em En | MEDLINE | ID: mdl-27164033
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biossíntese de Proteínas / Arabidopsis / Proteínas RGS / Proteínas de Arabidopsis Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biossíntese de Proteínas / Arabidopsis / Proteínas RGS / Proteínas de Arabidopsis Idioma: En Ano de publicação: 2016 Tipo de documento: Article