View source for 8hbg


==FMDV (A/TUR/14/98) in complex with M678F==
<StructureSection load='8hbg' size='340' side='right'caption='[[8hbg]], [[Resolution|resolution]] 3.60&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8hbg]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Foot-and-mouth_disease_virus_A Foot-and-mouth disease virus A] and [https://en.wikipedia.org/wiki/Lama_glama Lama glama]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8HBG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HBG FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.6&#8491;</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=8hbg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hbg OCA], [https://pdbe.org/8hbg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hbg RCSB], [https://www.ebi.ac.uk/pdbsum/8hbg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hbg ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/A0A7D5BJ70_9PICO A0A7D5BJ70_9PICO] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Unlike most other picornaviruses, foot-and-mouth disease (FMD) intact virions (146S) dissociate easily into small pentameric subunits (12S). This causes a dramatically decreased immunogenicity by a mechanism that remains elusive. Here, we present the high-resolution structures of 12S (3.2 A) and its immune complex of a single-domain antibody (VHH) targeting the particle interior (3.2 A), as well as two 146S-specific VHHs complexed to distinct sites on the 146S capsid surface (3.6 A and 2.9 A). The antigenic landscape of 146S is depicted using 13 known FMD virus-antibody complexes. Comparison of the immunogenicity of 146S and 12S in pigs, focusing on the resulting antigenic sites and incorporating structural analysis, reveals that dissociation of 146S leads to structural alteration and destruction of multiple epitopes, resulting in significant differences in antibody profiles/lineages induced by 12S and 146S. Furthermore, 146S generates higher synergistic neutralizing antibody titers compared to 12S, whereas both particles induce similar total FMD virus specific antibody titers. This study can guide the structure-based rational design of novel multivalent and broad-spectrum recombinant vaccines for protection against FMD.

Foot-and-mouth disease virus antigenic landscape and reduced immunogenicity elucidated in atomic detail.,Li H, Liu P, Dong H, Dekker A, Harmsen MM, Guo H, Wang X, Sun S Nat Commun. 2024 Oct 10;15(1):8774. doi: 10.1038/s41467-024-53027-5. PMID:39389971<ref>PMID:39389971</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 8hbg" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Foot-and-mouth disease virus A]]
[[Category: Lama glama]]
[[Category: Large Structures]]
[[Category: Dong H]]
[[Category: Li HZ]]
[[Category: Liu P]]