<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(10)</volume><submitter>Sipieter F</submitter><pubmed_abstract>Uncoupling of ERK1/2 phosphorylation from subcellular localization is essential towards the understanding of molecular mechanisms that control ERK1/2-mediated cell-fate decision. ERK1/2 non-catalytic functions and discoveries of new specific anchors responsible of the subcellular compartmentalization of ERK1/2 signaling pathway have been proposed as regulation mechanisms for which dynamic monitoring of ERK1/2 localization is necessary. However, studying the spatiotemporal features of ERK2, for instance, in different cellular processes in living cells and tissues requires a tool that can faithfully report on its subcellular distribution. We developed a novel molecular tool, ERK2-LOC, based on the T2A-mediated coexpression of strictly equimolar levels of eGFP-ERK2 and MEK1, to faithfully vis</pubmed_abstract><journal>PloS one</journal><pagination>e0140924</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4627772</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms.</pubmed_title><pmcid>PMC4627772</pmcid><pubmed_authors>Riquet FB</pubmed_authors><pubmed_authors>Cailliau-Maggio K</pubmed_authors><pubmed_authors>Gonzalez Pisfil M</pubmed_authors><pubmed_authors>Vandenabeele P</pubmed_authors><pubmed_authors>Bodart JF</pubmed_authors><pubmed_authors>Heliot L</pubmed_authors><pubmed_authors>Spriet C</pubmed_authors><pubmed_authors>Sipieter F</pubmed_authors><pubmed_authors>Cappe B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms.</name><description>Uncoupling of ERK1/2 phosphorylation from subcellular localization is essential towards the understanding of molecular mechanisms that control ERK1/2-mediated cell-fate decision. ERK1/2 non-catalytic functions and discoveries of new specific anchors responsible of the subcellular compartmentalization of ERK1/2 signaling pathway have been proposed as regulation mechanisms for which dynamic monitoring of ERK1/2 localization is necessary. However, studying the spatiotemporal features of ERK2, for instance, in different cellular processes in living cells and tissues requires a tool that can faithfully report on its subcellular distribution. We developed a novel molecular tool, ERK2-LOC, based on the T2A-mediated coexpression of strictly equimolar levels of eGFP-ERK2 and MEK1, to faithfully vis</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-04-19T06:10:42.049Z</modification><creation>2019-03-26T23:28:06Z</creation></dates><accession>S-EPMC4627772</accession><cross_references><pubmed>26517832</pubmed><doi>10.1371/journal.pone.0140924</doi></cross_references></HashMap>