| Literature DB >> 27924571 |
Abstract
Intercellular communication often involves phosphorylation of signal transduction proteins, including mitogen-activated protein kinases (MAPKs). Immunological detection of phosphorylated MAPK can be used to monitor signaling in vivo, identify novel pathway components, and assess ligand activity. In this chapter, I describe a cell co-culture method to assess activity of cell-bound extracellular ligands that result in phosphorylation of the ERK (extracellular signal-regulated kinase) MAPK in Drosophila. This protocol may be adaptable to other pathways and/or model systems.Entities:
Keywords: Co-culture; ERK; MAP kinase; S2 cells; Western blot; dp-ERK
Mesh:
Substances:
Year: 2017 PMID: 27924571 PMCID: PMC5588906 DOI: 10.1007/978-1-4939-6424-6_17
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745