6wmh

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'''Unreleased structure'''
 
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The entry 6wmh is ON HOLD until Paper Publication
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==Next generation monomeric IgG4 Fc==
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<StructureSection load='6wmh' size='340' side='right'caption='[[6wmh]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6wmh]] is a 2 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=6WMH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6WMH FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3&#8491;</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=6wmh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6wmh OCA], [https://pdbe.org/6wmh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6wmh RCSB], [https://www.ebi.ac.uk/pdbsum/6wmh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6wmh ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/IGHG4_HUMAN IGHG4_HUMAN]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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In a biologic therapeutic landscape that requires versatility in targeting specificity, valency and half-life modulation, the monomeric Fc fusion platform holds exciting potential for the creation of a class of monovalent protein therapeutics that includes fusion proteins and bispecific targeting molecules. Here we report a structure-guided approach to engineer monomeric Fc molecules to adapt multiple versions of half-life extension modifications. Co-crystal structures of these monomeric Fc variants with Fc neonatal receptor (FcRn) shed light into the binding interactions that could serve as a guide for engineering the half-life of antibody Fc fragments. These engineered monomeric Fc molecules also enabled the generation of a novel monovalent bispecific molecular design, which translated the FcRn binding enhancement to improvement of in vivo serum half-life.
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Authors: Oganesyan, V.Y., Shan, L., van Dyk, N., Dall'Acqua, W.F.
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In vivo pharmacokinetic enhancement of monomeric Fc and monovalent bispecific designs through structural guidance.,Shan L, Dyk NV, Haskins N, Cook KM, Rosenthal KL, Mazor R, Dragulin-Otto S, Jiang Y, Wu H, Dall'Acqua WF, Borrok MJ, Damschroder MM, Oganesyan V Commun Biol. 2021 Sep 8;4(1):1048. doi: 10.1038/s42003-021-02565-5. PMID:34497355<ref>PMID:34497355</ref>
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Description: Next generation monomeric IgG4 Fc
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Dall'Acqua, W.F]]
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<div class="pdbe-citations 6wmh" style="background-color:#fffaf0;"></div>
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[[Category: Oganesyan, V.Y]]
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== References ==
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[[Category: Shan, L]]
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<references/>
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[[Category: Van Dyk, N]]
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Dall'Acqua WF]]
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[[Category: Oganesyan VY]]
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[[Category: Shan L]]
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[[Category: Van Dyk N]]

Current revision

Next generation monomeric IgG4 Fc

PDB ID 6wmh

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