View source for 8te5


==Crystal structure of a multiple lysine-to-arginine substitution mutant of the human CRIg C3b-binding domain==
<StructureSection load='8te5' size='340' side='right'caption='[[8te5]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8te5]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8TE5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8TE5 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.502&#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=8te5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8te5 OCA], [https://pdbe.org/8te5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8te5 RCSB], [https://www.ebi.ac.uk/pdbsum/8te5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8te5 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/VSIG4_HUMAN VSIG4_HUMAN] Phagocytic receptor, strong negative regulator of T-cell proliferation and IL2 production. Potent inhibitor of the alternative complement pathway convertases.<ref>PMID:17016562</ref> <ref>PMID:17051150</ref> 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The extracellular region of the complement receptor of the Ig superfamily (CRIg) binds to certain C3 cleavage products (C3b, iC3b, C3c) and inhibits the alternative pathway (AP) of complement. In this study, we provide further insight into the CRIg protein and describe two CRIg mutants that lack multiple lysine residues as a means of facilitating chemical modifications of the protein. Structural analyses confirmed preservation of the native CRIg architecture in both mutants. In contrast to earlier reports suggesting that CRIg binds to C3b with an affinity of approximately 1 muM, we found that wild-type CRIg binds to C3b and iC3b with affinities &lt;100 nM, but to C3c with an affinity closer to 1 muM. We observed this same trend for both lysine substitution mutants, albeit with an apparent approximately 2- to 3-fold loss of affinity when compared with wild-type CRIg. Using flow cytometry, we confirmed binding to C3 fragment-opsonized Staphylococcus aureus cells by each mutant, again with an approximately 2- to 3-fold decrease when compared with wild-type. Whereas wild-type CRIg inhibits AP-driven lysis of rabbit erythrocytes with an IC50 of 1.6 muM, we observed an approximately 3-fold reduction in inhibition for both mutants. Interestingly, we found that amine-reactive crosslinking of the CRIg mutant containing only a single lysine results in a significant improvement in inhibitory potency across all concentrations examined when compared with the unmodified mutant, but in a manner sensitive to the length of the crosslinker. Collectively, our findings provide new insights into the CRIg protein and suggest an approach for engineering increasingly potent CRIg-based inhibitors of the AP.

New Insights into the Complement Receptor of the Ig Superfamily Obtained from Structural and Functional Studies on Two Mutants.,Duan H, Abram TG, Cruz AR, Rooijakkers SHM, Geisbrecht BV Immunohorizons. 2023 Nov 1;7(11):806-818. doi: 10.4049/immunohorizons.2300064. PMID:38032267<ref>PMID:38032267</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 8te5" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Abram TG]]
[[Category: Geisbrecht BV]]