4gg8
From Proteopedia
(Difference between revisions)
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==Immune Receptor== | ==Immune Receptor== | ||
- | <StructureSection load='4gg8' size='340' side='right'caption='[[4gg8]] | + | <StructureSection load='4gg8' size='340' side='right'caption='[[4gg8]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'> | + | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4GG8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4GG8 FirstGlance]. <br> |
- | </td></tr> | + | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4gg8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gg8 OCA], [https://pdbe.org/4gg8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4gg8 RCSB], [https://www.ebi.ac.uk/pdbsum/4gg8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4gg8 ProSAT]</span></td></tr> |
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- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4gg8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gg8 OCA], [https://pdbe.org/4gg8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4gg8 RCSB], [https://www.ebi.ac.uk/pdbsum/4gg8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4gg8 ProSAT]</span></td></tr> | + | |
</table> | </table> | ||
- | <div style="background-color:#fffaf0;"> | ||
- | == Publication Abstract from PubMed == | ||
- | Celiac disease is a human leukocyte antigen (HLA)-DQ2- and/or DQ8-associated T cell-mediated disorder that is induced by dietary gluten. Although it is established how gluten peptides bind HLA-DQ8 and HLA-DQ2, it is unclear how such peptide-HLA complexes are engaged by the T cell receptor (TCR), a recognition event that triggers disease pathology. We show that biased TCR usage (TRBV9( *)01) underpins the recognition of HLA-DQ8-alpha-I-gliadin. The structure of a prototypical TRBV9( *)01-TCR-HLA-DQ8-alpha-I-gliadin complex shows that the TCR docks centrally above HLA-DQ8-alpha-I-gliadin, in which all complementarity-determining region-beta (CDRbeta) loops interact with the gliadin peptide. Mutagenesis at the TRBV9( *)01-TCR-HLA-DQ8-alpha-I-gliadin interface provides an energetic basis for the Vbeta bias. Moreover, CDR3 diversity accounts for TRBV9( *)01(+) TCRs exhibiting differing reactivities toward the gliadin epitopes at various deamidation states. Accordingly, biased TCR usage is an important factor in the pathogenesis of DQ8-mediated celiac disease. | ||
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- | Biased T Cell Receptor Usage Directed against Human Leukocyte Antigen DQ8-Restricted Gliadin Peptides Is Associated with Celiac Disease.,Broughton SE, Petersen J, Theodossis A, Scally SW, Loh KL, Thompson A, van Bergen J, Kooy-Winkelaar Y, Henderson KN, Beddoe T, Tye-Din JA, Mannering SI, Purcell AW, McCluskey J, Anderson RP, Koning F, Reid HH, Rossjohn J Immunity. 2012 Oct 19;37(4):611-21. doi: 10.1016/j.immuni.2012.07.013. Epub 2012 , Oct 11. PMID:23063329<ref>PMID:23063329</ref> | ||
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- | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
- | </div> | ||
- | <div class="pdbe-citations 4gg8" style="background-color:#fffaf0;"></div> | ||
==See Also== | ==See Also== | ||
*[[T-cell receptor 3D structures|T-cell receptor 3D structures]] | *[[T-cell receptor 3D structures|T-cell receptor 3D structures]] | ||
- | == References == | ||
- | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Broughton | + | [[Category: Broughton SE]] |
- | [[Category: Petersen | + | [[Category: Petersen J]] |
- | [[Category: Reid | + | [[Category: Reid HH]] |
- | [[Category: Rossjohn | + | [[Category: Rossjohn J]] |
- | [[Category: Theodossis | + | [[Category: Theodossis A]] |
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Revision as of 10:42, 31 August 2022
Immune Receptor
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