Measuring agonist-induced ERK MAP kinase phosphorylation for G-protein-coupled receptors

Methods Cell Biol. 2019:149:141-153. doi: 10.1016/bs.mcb.2018.09.015. Epub 2018 Nov 19.

Abstract

Agonist stimulation of G-protein-coupled receptors (GPCRs) typically results in phosphorylation and activation of ERK (Extracellular-signal Regulated Kinase) which is a member of MAP kinase (Mitogen-Activated Protein kinase) family. Detection of phosphorylated ERK1/2 MAP kinase has been widely used as readout of GPCR signaling in heterologous cells, primary cells, tissues and even in animal studies. ERK1/2 phosphorylation downstream of GPCRs is now well established to arise from the activation of both, the heterotrimeric G-proteins and β-arrestins (βarrs) with distinct spatio-temporal components. Here, we present a step-by-step protocol for measuring agonist-induced ERK1/2 MAP kinase activation downstream of GPCRs using standard Western blotting assay. Note: ERK1/2 is also referred to as p44/42 MAP kinase. ERK1 and ERK2 are same as Mitogen-Activated Protein Kinase 3 (MAP3) and Mitogen-Activated Protein Kinase 1 (MAP1), respectively.

Keywords: ERK MAP kinase; GPCRs; Signaling; β-arrestins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation
  • Cytological Techniques / methods*
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • HEK293 Cells
  • Humans
  • Phosphorylation
  • Polyethyleneimine / chemistry
  • Receptors, G-Protein-Coupled / agonists*

Substances

  • Receptors, G-Protein-Coupled
  • Polyethyleneimine
  • Extracellular Signal-Regulated MAP Kinases