Crystal structures of two H-2Db/glycopeptide complexes suggest a molecular basis for CTL cross-reactivity (Q27639770)

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Mark R Wormald

object named as

M Wormald

10

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author name string

A Glithero

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J Tormo

2

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J S Haurum

3

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G Arsequell

4

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G Valencia

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J Edwards

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Y L Pao

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R A Dwek

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E Y Jones

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T Elliott

Immunization with glycosylated Kb-binding peptides generates carbohydrate-specific, unrestricted cytotoxic T cells

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language of work or name

English

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publication date

January 1999

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published in

Immunity

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volume

10

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page(s)

63-74

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issue

1

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cites work

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In thymic selection, peptide diversity gives and takes away

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Molecular basis for the recognition of two structurally different major histocompatibility complex/peptide complexes by a single T-cell receptor

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Epitope glycosylation plays a critical role for T cell recognition of type II collagen in collagen-induced arthritis.

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Two human T cell receptors bind in a similar diagonal mode to the HLA-A2/Tax peptide complex using different TCR amino acids

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Carbohydrate-dependent, HLA class II-restricted, human T cell response to the bee venom allergen phospholipase A2 in allergic patients.

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Cytotoxic T lymphocytes recognize a reconstituted class I histocompatibility antigen (HLA-A2) as an allogeneic target molecule

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Crystal structures of two viral peptides in complex with murine MHC class I H-2Kb

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Five viral peptide-HLA-A2 co-crystals. Simultaneous space group determination and X-ray data collection

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Structure of the complex between human T-cell receptor, viral peptide and HLA-A2

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An alphabeta T cell receptor structure at 2.5 A and its orientation in the TCR-MHC complex

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Structural basis of plasticity in T cell receptor recognition of a self peptide-MHC antigen

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Glycosylation in the nucleus and cytoplasm

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O-GlcNAcylation of key nuclear and cytoskeletal proteins: reciprocity with O-phosphorylation and putative roles in protein multimerization

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Recognition of carbohydrate by major histocompatibility complex class I-restricted, glycopeptide-specific cytotoxic T lymphocytes

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Peptide anchor residue glycosylation: effect on class I major histocompatibility complex binding and cytotoxic T lymphocyte recognition

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Improved methods for building protein models in electron density maps and the location of errors in these models

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Protection against lethal Sendai virus infection by in vivo priming of virus-specific cytotoxic T lymphocytes with a free synthetic peptide

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The three-dimensional structure of peptide-MHC complexes

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A very high level of crossreactivity is an essential feature of the T-cell receptor

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T cell recognition of carbohydrates on type II collagen

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AMoRe: an automated package for molecular replacement

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Processing of X-ray diffraction data collected in oscillation mode

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Carbohydrate-binding proteins: tertiary structures and protein-sugar interactions

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A soluble major histocompatibility complex class I peptide-binding platform undergoes a conformational change in response to peptide epitopes.

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Exact prediction of a natural T cell epitope

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Autoimmune diseases: the failure of self tolerance

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Bound water structure and polymorphic amino acids act together to allow the binding of different peptides to MHC class I HLA-B53

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Fast Association Rates Suggest a Conformational Change in the MHC Class I Molecule H-2Dbupon Peptide Binding

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Multiple sclerosis: a coordinated immunological attack against myelin in the central nervous system

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Crystal structure of cat muscle pyruvate kinase at a resolution of 2.6 A

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Identification of a common docking topology with substantial variation among different TCR-peptide-MHC complexes

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Cloning of the mycobacterial epitope recognized by T lymphocytes in adjuvant arthritis

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Variations in oligosaccharide-protein interactions in immunoglobulin G determine the site-specific glycosylation profiles and modulate the dynamic motion of the Fc oligosaccharides

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The three-dimensional structure of H-2Db at 2.4 A resolution: implications for antigen-determinant selection

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GD2 oligosaccharide: target for cytotoxic T lymphocytes

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