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==Crystal structure of anti-gliadin 1002-1E03 Fab fragment in complex of peptide PLQPEQPFP==
==Crystal structure of anti-gliadin 1002-1E03 Fab fragment in complex of peptide PLQPEQPFP==
<StructureSection load='5ijk' size='340' side='right' caption='[[5ijk]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
<StructureSection load='5ijk' size='340' side='right'caption='[[5ijk]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[5ijk]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5IJK OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5IJK FirstGlance]. <br>
<table><tr><td colspan='2'>[[5ijk]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Triticum_aestivum Triticum aestivum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5IJK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5IJK FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5ifj|5ifj]], [[5ig7|5ig7]], [[5ihz|5ihz]]</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5ijk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ijk OCA], [http://pdbe.org/5ijk PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5ijk RCSB], [http://www.ebi.ac.uk/pdbsum/5ijk PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5ijk ProSAT]</span></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=5ijk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ijk OCA], [https://pdbe.org/5ijk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5ijk RCSB], [https://www.ebi.ac.uk/pdbsum/5ijk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5ijk ProSAT]</span></td></tr>
</table>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The role of B cells and posttranslational modifications in pathogenesis of organ-specific immune diseases is increasingly envisioned but remains poorly understood, particularly in human disorders. In celiac disease, transglutaminase 2-modified (TG2-modified; deamidated) gluten peptides drive disease-specific T cell and B cell responses, and antibodies to deamidated gluten peptides are excellent diagnostic markers. Here, we substantiate by high-throughput sequencing of IGHV genes that antibodies to a disease-specific, deamidated, and immunodominant B cell epitope of gluten (PLQPEQPFP) have biased and stereotyped usage of IGHV3-23 and IGHV3-15 gene segments with modest somatic mutations. X-ray crystal structures of 2 prototype IGHV3-15/IGKV4-1 and IGHV3-23/IGLV4-69 antibodies reveal peptide interaction mainly via germline-encoded residues. In-depth mutational analysis showed restricted selection and substitution patterns at positions involved in antigen binding. While the IGHV3-15/IGKV4-1 antibody interacts with Glu5 and Gln6, the IGHV3-23/IGLV4-69 antibody interacts with Gln3, Pro4, Pro7, and Phe8 - residues involved in substrate recognition by TG2. Hence, both antibodies, despite different interaction with the epitope, recognize signatures of TG2 processing that facilitates B cell presentation of deamidated gluten peptides to T cells, thereby providing a molecular framework for the generation of these clinically important antibodies. The study provides essential insight into the pathogenic mechanism of celiac disease.
Stereotyped antibody responses target posttranslationally modified gluten in celiac disease.,Snir O, Chen X, Gidoni M, du Pre MF, Zhao Y, Steinsbo O, Lundin KE, Yaari G, Sollid LM JCI Insight. 2017 Sep 7;2(17). pii: 93961. doi: 10.1172/jci.insight.93961. PMID:28878138<ref>PMID:28878138</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 5ijk" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Chen, X]]
[[Category: Homo sapiens]]
[[Category: Harlos, K]]
[[Category: Large Structures]]
[[Category: Snir, O]]
[[Category: Triticum aestivum]]
[[Category: Sollid, L M]]
[[Category: Chen X]]
[[Category: Zhao, Y]]
[[Category: Gidoni M]]
[[Category: Anti-gliadin antibody]]
[[Category: Lundin KE]]
[[Category: Celiac disease]]
[[Category: Snir O]]
[[Category: Immune system]]
[[Category: Sollid LM]]
[[Category: Steinsbo O]]
[[Category: Yaari G]]
[[Category: Zhao Y]]
[[Category: Du Pre MF]]

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