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Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms
by
Sipieter, François
, Gonzalez Pisfil, Mariano
, Héliot, Laurent
, Bodart, Jean-François
, Vandenabeele, Peter
, Spriet, Corentin
, Cailliau-Maggio, Katia
, Riquet, Franck B.
, Cappe, Benjamin
in
Animals
/ Apoptosis
/ Catalysis
/ Cell Differentiation
/ Cells (biology)
/ Cytoplasm
/ Developmental stages
/ Embryos
/ Extracellular signal-regulated kinase
/ Fluorescence
/ Fluorescence microscopy
/ Genes, Reporter
/ Inflammation
/ Journalists
/ Kinases
/ Lasers
/ Life Sciences
/ Localization
/ MAP kinase
/ MAP Kinase Kinase 1 - genetics
/ MAP Kinase Kinase 1 - metabolism
/ MAP Kinase Signaling System
/ Mice
/ Mitogen-Activated Protein Kinase 1 - genetics
/ Mitogen-Activated Protein Kinase 1 - metabolism
/ Molecular biology
/ Molecular modelling
/ Monitoring
/ NIH 3T3 Cells
/ Phosphorylation
/ Proteins
/ Recovery (Medical)
/ Regulation
/ Signal Transduction
/ Signaling
/ Single-Cell Analysis - methods
/ Tissues
/ Xenopus laevis - embryology
/ Xenopus laevis - metabolism
/ Xenopus Proteins - metabolism
2015
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Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms
by
Sipieter, François
, Gonzalez Pisfil, Mariano
, Héliot, Laurent
, Bodart, Jean-François
, Vandenabeele, Peter
, Spriet, Corentin
, Cailliau-Maggio, Katia
, Riquet, Franck B.
, Cappe, Benjamin
in
Animals
/ Apoptosis
/ Catalysis
/ Cell Differentiation
/ Cells (biology)
/ Cytoplasm
/ Developmental stages
/ Embryos
/ Extracellular signal-regulated kinase
/ Fluorescence
/ Fluorescence microscopy
/ Genes, Reporter
/ Inflammation
/ Journalists
/ Kinases
/ Lasers
/ Life Sciences
/ Localization
/ MAP kinase
/ MAP Kinase Kinase 1 - genetics
/ MAP Kinase Kinase 1 - metabolism
/ MAP Kinase Signaling System
/ Mice
/ Mitogen-Activated Protein Kinase 1 - genetics
/ Mitogen-Activated Protein Kinase 1 - metabolism
/ Molecular biology
/ Molecular modelling
/ Monitoring
/ NIH 3T3 Cells
/ Phosphorylation
/ Proteins
/ Recovery (Medical)
/ Regulation
/ Signal Transduction
/ Signaling
/ Single-Cell Analysis - methods
/ Tissues
/ Xenopus laevis - embryology
/ Xenopus laevis - metabolism
/ Xenopus Proteins - metabolism
2015
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Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms
by
Sipieter, François
, Gonzalez Pisfil, Mariano
, Héliot, Laurent
, Bodart, Jean-François
, Vandenabeele, Peter
, Spriet, Corentin
, Cailliau-Maggio, Katia
, Riquet, Franck B.
, Cappe, Benjamin
in
Animals
/ Apoptosis
/ Catalysis
/ Cell Differentiation
/ Cells (biology)
/ Cytoplasm
/ Developmental stages
/ Embryos
/ Extracellular signal-regulated kinase
/ Fluorescence
/ Fluorescence microscopy
/ Genes, Reporter
/ Inflammation
/ Journalists
/ Kinases
/ Lasers
/ Life Sciences
/ Localization
/ MAP kinase
/ MAP Kinase Kinase 1 - genetics
/ MAP Kinase Kinase 1 - metabolism
/ MAP Kinase Signaling System
/ Mice
/ Mitogen-Activated Protein Kinase 1 - genetics
/ Mitogen-Activated Protein Kinase 1 - metabolism
/ Molecular biology
/ Molecular modelling
/ Monitoring
/ NIH 3T3 Cells
/ Phosphorylation
/ Proteins
/ Recovery (Medical)
/ Regulation
/ Signal Transduction
/ Signaling
/ Single-Cell Analysis - methods
/ Tissues
/ Xenopus laevis - embryology
/ Xenopus laevis - metabolism
/ Xenopus Proteins - metabolism
2015
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Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms
Journal Article
Novel Reporter for Faithful Monitoring of ERK2 Dynamics in Living Cells and Model Organisms
2015
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Overview
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 visualize ERK2 localization patterns. MEK1 and eGFP-ERK2 were expressed reliably and functionally both in vitro and in single living cells. We then assessed the subcellular distribution and mobility of ERK2-LOC using fluorescence microscopy in non-stimulated conditions and after activation/inhibition of the MAPK/ERK1/2 signaling pathway. Finally, we used our coexpression system in Xenopus laevis embryos during the early stages of development. This is the first report on MEK1/ERK2 T2A-mediated coexpression in living embryos, and we show that there is a strong correlation between the spatiotemporal subcellular distribution of ERK2-LOC and the phosphorylation patterns of ERK1/2. Our approach can be used to study the spatiotemporal localization of ERK2 and its dynamics in a variety of processes in living cells and embryonic tissues.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
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