7y09

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (06:30, 3 July 2025) (edit) (undo)
 
(4 intermediate revisions not shown.)
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 7y09 is ON HOLD until Paper Publication
+
==Cryo-EM structure of human IgM-Fc in complex with the J chain and the DBL domain of DBLMSP==
 +
<StructureSection load='7y09' size='340' side='right'caption='[[7y09]], [[Resolution|resolution]] 3.71&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[7y09]] is a 12 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Plasmodium_falciparum Plasmodium falciparum]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7Y09 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7Y09 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]] 3.71&#8491;</td></tr>
 +
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></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=7y09 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7y09 OCA], [https://pdbe.org/7y09 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7y09 RCSB], [https://www.ebi.ac.uk/pdbsum/7y09 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7y09 ProSAT]</span></td></tr>
 +
</table>
 +
<div style="background-color:#fffaf0;">
 +
== Publication Abstract from PubMed ==
 +
Plasmodium falciparum causes the most severe malaria in humans. Immunoglobulin M (IgM) serves as the first line of humoral defense against infection and potently activates the complement pathway to facilitate P. falciparum clearance. A number of P. falciparum proteins bind IgM, leading to immune evasion and severe disease. However, the underlying molecular mechanisms remain unknown. Here, using high-resolution cryo-electron microscopy, we delineate how P. falciparum proteins VAR2CSA, TM284VAR1, DBLMSP, and DBLMSP2 target IgM. Each protein binds IgM in a different manner, and together they present a variety of Duffy-binding-like domain-IgM interaction modes. We further show that these proteins interfere directly with IgM-mediated complement activation in vitro, with VAR2CSA exhibiting the most potent inhibitory effect. These results underscore the importance of IgM for human adaptation of P. falciparum and provide critical insights into its immune evasion mechanism.
-
Authors:
+
Plasmodium falciparum has evolved multiple mechanisms to hijack human immunoglobulin M.,Ji C, Shen H, Su C, Li Y, Chen S, Sharp TH, Xiao J Nat Commun. 2023 May 8;14(1):2650. doi: 10.1038/s41467-023-38320-z. PMID:37156765<ref>PMID:37156765</ref>
-
Description:
+
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
-
[[Category: Unreleased Structures]]
+
</div>
 +
<div class="pdbe-citations 7y09" style="background-color:#fffaf0;"></div>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Homo sapiens]]
 +
[[Category: Large Structures]]
 +
[[Category: Plasmodium falciparum]]
 +
[[Category: Ji C]]
 +
[[Category: Shen H]]
 +
[[Category: Xiao J]]

Current revision

Cryo-EM structure of human IgM-Fc in complex with the J chain and the DBL domain of DBLMSP

PDB ID 7y09

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools