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Single-molecule dynamics of Dishevelled at the plasma membrane and Wnt pathway activation
by
Chen, Maorong
, Angers, Stephane
, He, Xi
, Kirschner, Marc W.
, Steinhart, Zachary
, Ma, Wenzhe
in
Activation
/ Biological Sciences
/ Cell Membrane - chemistry
/ Cell Membrane - genetics
/ Cell Membrane - metabolism
/ Coordination compounds
/ CRISPR
/ Deactivation
/ Dishevelled protein
/ Dishevelled Proteins - chemistry
/ Dishevelled Proteins - genetics
/ Dishevelled Proteins - metabolism
/ Dwell time
/ Dynamic stability
/ Fluorescence
/ HEK293 Cells
/ Homologous recombination
/ Homology
/ Humans
/ Inactivation
/ Ligands
/ Low Density Lipoprotein Receptor-Related Protein-5 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-5 - metabolism
/ Low Density Lipoprotein Receptor-Related Protein-6 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-6 - metabolism
/ LRP5 protein
/ Membranes
/ Monomers
/ Oligomerization
/ Protein Binding
/ Signal transduction
/ Single Molecule Imaging
/ Systems Biology
/ Wnt protein
/ Wnt Signaling Pathway
/ Wnt3A Protein - chemistry
/ Wnt3A Protein - genetics
/ Wnt3A Protein - metabolism
/ β-Catenin
2020
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Single-molecule dynamics of Dishevelled at the plasma membrane and Wnt pathway activation
by
Chen, Maorong
, Angers, Stephane
, He, Xi
, Kirschner, Marc W.
, Steinhart, Zachary
, Ma, Wenzhe
in
Activation
/ Biological Sciences
/ Cell Membrane - chemistry
/ Cell Membrane - genetics
/ Cell Membrane - metabolism
/ Coordination compounds
/ CRISPR
/ Deactivation
/ Dishevelled protein
/ Dishevelled Proteins - chemistry
/ Dishevelled Proteins - genetics
/ Dishevelled Proteins - metabolism
/ Dwell time
/ Dynamic stability
/ Fluorescence
/ HEK293 Cells
/ Homologous recombination
/ Homology
/ Humans
/ Inactivation
/ Ligands
/ Low Density Lipoprotein Receptor-Related Protein-5 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-5 - metabolism
/ Low Density Lipoprotein Receptor-Related Protein-6 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-6 - metabolism
/ LRP5 protein
/ Membranes
/ Monomers
/ Oligomerization
/ Protein Binding
/ Signal transduction
/ Single Molecule Imaging
/ Systems Biology
/ Wnt protein
/ Wnt Signaling Pathway
/ Wnt3A Protein - chemistry
/ Wnt3A Protein - genetics
/ Wnt3A Protein - metabolism
/ β-Catenin
2020
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Single-molecule dynamics of Dishevelled at the plasma membrane and Wnt pathway activation
by
Chen, Maorong
, Angers, Stephane
, He, Xi
, Kirschner, Marc W.
, Steinhart, Zachary
, Ma, Wenzhe
in
Activation
/ Biological Sciences
/ Cell Membrane - chemistry
/ Cell Membrane - genetics
/ Cell Membrane - metabolism
/ Coordination compounds
/ CRISPR
/ Deactivation
/ Dishevelled protein
/ Dishevelled Proteins - chemistry
/ Dishevelled Proteins - genetics
/ Dishevelled Proteins - metabolism
/ Dwell time
/ Dynamic stability
/ Fluorescence
/ HEK293 Cells
/ Homologous recombination
/ Homology
/ Humans
/ Inactivation
/ Ligands
/ Low Density Lipoprotein Receptor-Related Protein-5 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-5 - metabolism
/ Low Density Lipoprotein Receptor-Related Protein-6 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-6 - metabolism
/ LRP5 protein
/ Membranes
/ Monomers
/ Oligomerization
/ Protein Binding
/ Signal transduction
/ Single Molecule Imaging
/ Systems Biology
/ Wnt protein
/ Wnt Signaling Pathway
/ Wnt3A Protein - chemistry
/ Wnt3A Protein - genetics
/ Wnt3A Protein - metabolism
/ β-Catenin
2020
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Single-molecule dynamics of Dishevelled at the plasma membrane and Wnt pathway activation
Journal Article
Single-molecule dynamics of Dishevelled at the plasma membrane and Wnt pathway activation
2020
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Overview
Dvl (Dishevelled) is one of several essential nonenzymatic components of the Wnt signaling pathway. In most current models, Dvl forms complexes with Wnt ligand receptors, Fzd and LRP5/6 at the plasma membrane, which then recruits the destruction complex, eventually leading to inactivation of β-catenin degradation. Although this model is widespread, direct evidence for the individual steps is lacking. In this study, we tagged mEGFP to C terminus of dishevelled2 gene using CRISPR/Cas9-induced homologous recombination and observed its dynamics directly at the single-molecule level with total internal reflection fluorescence (TIRF) microscopy. We focused on two questions: 1) What is the native size and what are the dynamic features of membrane-bound Dvl complexes during Wnt pathway activation? 2) What controls the behavior of these complexes? We found that membrane-bound Dvl2 is predominantly monomer in the absence of Wnt (observed mean size 1.1). Wnt3a stimulation leads to an increase in the total concentration of membrane-bound Dvl2 from 0.12/μm² to 0.54/μm². Wnt3a also leads to increased oligomerization which raises the weighted mean size of Dvl2 complexes to 1.5, with 56.1% of Dvl still as monomers. The driving force for Dvl2 oligomerization is the increased concentration of membrane Dvl2 caused by increased affinity of Dvl2 for Fzd, which is independent of LRP5/6. The oligomerized Dvl2 complexes have increased dwell time, 2 ∼ 3 min, compared to less than 1 s for monomeric Dvl2. These properties make Dvl a unique scaffold, dynamically changing its state of assembly and stability at the membrane in response to Wnt ligands.
Publisher
National Academy of Sciences
Subject
/ CRISPR
/ Dishevelled Proteins - chemistry
/ Dishevelled Proteins - genetics
/ Dishevelled Proteins - metabolism
/ Homology
/ Humans
/ Ligands
/ Low Density Lipoprotein Receptor-Related Protein-5 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-5 - metabolism
/ Low Density Lipoprotein Receptor-Related Protein-6 - genetics
/ Low Density Lipoprotein Receptor-Related Protein-6 - metabolism
/ Monomers
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