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The Immune Synapse

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Cover of 'The Immune Synapse'

Table of Contents

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    Book Overview
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    Chapter 1 The Immune Synapse: Past, Present, and Future
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    Chapter 2 Analyzing Actin Dynamics at the Immunological Synapse
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    Chapter 3 Analysis of Microtubules and Microtubule-Organizing Center at the Immune Synapse
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    Chapter 4 Analyzing the Dynamics of Signaling Microclusters
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    Chapter 5 Reconstitution of TCR Signaling Using Supported Lipid Bilayers
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    Chapter 6 Plasma Membrane Sheets for Studies of B Cell Antigen Internalization from Immune Synapses
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    Chapter 7 Studying the Dynamics of TCR Internalization at the Immune Synapse
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    Chapter 8 T Cell Receptor Activation of NF-κB in Effector T Cells: Visualizing Signaling Events Within and Beyond the Cytoplasmic Domain of the Immunological Synapse
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    Chapter 9 Imaging Vesicular Traffic at the Immune Synapse
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    Chapter 10 Analysis of TCR/CD3 Recycling at the Immune Synapse
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    Chapter 11 Simultaneous Membrane Capacitance Measurements and TIRF Microscopy to Study Granule Trafficking at Immune Synapses
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    Chapter 12 Mathematical Modeling of Synaptic Patterns
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    Chapter 13 Super-resolution Analysis of TCR-Dependent Signaling: Single-Molecule Localization Microscopy
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    Chapter 14 Förster Resonance Energy Transfer to Study TCR-pMHC Interactions in the Immunological Synapse
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    Chapter 15 Two-Dimensional Analysis of Cross-Junctional Molecular Interaction by Force Probes
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    Chapter 16 Studying Dynamic Plasma Membrane Binding of TCR-CD3 Chains During Immunological Synapse Formation Using Donor-Quenching FRET and FLIM-FRET
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    Chapter 17 Revealing the Role of Microscale Architecture in Immune Synapse Function Through Surface Micropatterning
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    Chapter 18 Spatial Control of Biological Ligands on Surfaces Applied to T Cell Activation
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    Chapter 19 Probing Synaptic Biomechanics Using Micropillar Arrays
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    Chapter 20 Microchannels for the Study of T Cell Immunological Synapses and Kinapses
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    Chapter 21 Purification of LAT-Containing Membranes from Resting and Activated T Lymphocytes
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    Chapter 22 Quantitative Phosphoproteomic Analysis of T-Cell Receptor Signaling
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    Chapter 23 Imaging Asymmetric T Cell Division
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    Chapter 24 Ultrastructure of Immune Synapses
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    Chapter 25 Systems Imaging of the Immune Synapse
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    Chapter 26 Comprehensive Analysis of Immunological Synapse Phenotypes Using Supported Lipid Bilayers
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    Chapter 27 Studying Immunoreceptor Signaling in Human T Cells Using Electroporation of In Vitro Transcribed mRNA
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    Chapter 28 A Protein Expression Toolkit for Studying Signaling in T Cells
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    Chapter 29 Imaging the Effector CD8 Synapse
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    Chapter 30 The Mast Cell Antibody-Dependent Degranulatory Synapse
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    Chapter 31 Measurement of Lytic Granule Convergence After Formation of an NK Cell Immunological Synapse
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    Chapter 32 Studying the T Cell-Astrocyte Immune Synapse
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    Chapter 33 Aberrant Immunological Synapses Driven by Leukemic Antigen-Presenting Cells
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    Chapter 34 Studying the Immune Synapse in HIV-1 Infection
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    Chapter 35 In Vivo Imaging of T Cell Immunological Synapses and Kinapses in Lymph Nodes
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    Chapter 36 Studying Dendritic Cell-T Cell Interactions Under In Vivo Conditions
Attention for Chapter 21: Purification of LAT-Containing Membranes from Resting and Activated T Lymphocytes
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Chapter title
Purification of LAT-Containing Membranes from Resting and Activated T Lymphocytes
Chapter number 21
Book title
The Immune Synapse
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6881-7_21
Pubmed ID
Book ISBNs
978-1-4939-6879-4, 978-1-4939-6881-7
Authors

Claire Hivroz, Paola Larghi, Mabel Jouve, Laurence Ardouin

Editors

Cosima T. Baldari, Michael L. Dustin

Abstract

In T lymphocytes, the immune synapse is an active zone of vesicular traffic. Directional transport of vesicular receptors and signaling molecules from or to the immune synapse has been shown to play an important role in T-cell receptor (TCR) signal transduction. However, how vesicular trafficking is regulating the activation of T cells is still a burning question, and the characterization of these intracellular compartments remains the first step to understand this process. We describe herein a protocol, which combines a separation of membranes on flotation gradient with an affinity purification of Strep-tagged fusion transmembrane proteins with Strep-Tactin(®) resin, allowing the purification of membranes containing the Strep-tagged molecule of interest. By keeping the membranes intact, this protocol leads to the purification of molecules physically associated with the Strep-tagged protein as well as of molecules present in the same membrane compartment: transmembrane proteins, proteins strongly associated with the membranes, and luminal proteins. The example shown herein is the purification of membrane compartment prepared from T lymphocytes expressing LAT fused to a Strep-tag.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 50%
Student > Master 2 20%
Student > Doctoral Student 1 10%
Unknown 2 20%
Readers by discipline Count As %
Immunology and Microbiology 3 30%
Agricultural and Biological Sciences 3 30%
Biochemistry, Genetics and Molecular Biology 2 20%
Unknown 2 20%