(Q46020608)

18 December 2017

title

Direct observation of ligand recognition by T cells. (English)

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18 December 2017

author name string

Darrell J Irvine

1

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18 December 2017

Marco A Purbhoo

2

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18 December 2017

Michelle Krogsgaard

3

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18 December 2017

Mark M Davis

4

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18 December 2017

language of work or name

English

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publication date

1 October 2002

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18 December 2017

published in

Nature

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18 December 2017

volume

419

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18 December 2017

page(s)

845-849

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18 December 2017

issue

6909

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18 December 2017

https://scigraph.springernature.com/pub.10.1038/nature01076

exact match

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cites work

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The immunological synapse: a molecular machine controlling T cell activation

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Differential clustering of CD4 and CD3zeta during T cell recognition

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Quantitation of antigen-presenting cell MHC class II/peptide complexes necessary for T-cell stimulation

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The minimal number of class II MHC-antigen complexes needed for T cell activation

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The minimal number of antigen-major histocompatibility complex class II complexes required for activation of naive and primed T cells

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Determination of the relationship between T cell responsiveness and the number of MHC-peptide complexes using specific monoclonal antibodies

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7 January 2021

Peptide binding to class I MHC on living cells and quantitation of complexes required for CTL lysis

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Minimal requirements for peptide mediated activation of CD8+ CTL.

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Evidence that a single peptide-MHC complex on a target cell can elicit a cytolytic T cell response

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7 January 2021

Phycobiliprotein-Fab conjugates as probes for single particle fluorescence imaging

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Single-molecule imaging of EGFR signalling on the surface of living cells

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Fluorescent probes of cell signaling

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Polarity of T cell shape, motility, and sensitivity to antigen

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Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition

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The major histocompatibility complex-restricted antigen receptor on T cells. II. Role of the L3T4 product

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CD4 augments the response of a T cell to agonist but not to antagonist ligands

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Initiation of signal transduction through the T cell receptor requires the multivalent engagement of peptide/MHC ligands [corrected]

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The relationship of MHC-peptide binding and T cell activation probed using chemically defined MHC class II oligomers

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Crystal structure of the human CD4 N-terminal two-domain fragment complexed to a class II MHC molecule

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T Cell Receptor Binding to a pMHCII Ligand Is Kinetically Distinct from and Independent of CD4.

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Detection of antigen-specific T cells with multivalent soluble class II MHC covalent peptide complexes.

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Visualizing the dynamics of T cell activation: intracellular adhesion molecule 1 migrates rapidly to the T cell/B cell interface and acts to sustain calcium levels

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Production of high-titer helper-free retroviruses by transient transfection

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A receptor/cytoskeletal movement triggered by costimulation during T cell activation

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Identifiers

DOI

10.1038/NATURE01076

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18 December 2017

Dimensions Publication ID

0 references

1 reference

18 December 2017