6uqc

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m (Protected "6uqc" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6uqc is ON HOLD
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==Mouse IgG2a Bispecific Fc==
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<StructureSection load='6uqc' size='340' side='right'caption='[[6uqc]], [[Resolution|resolution]] 1.87&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6uqc]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6UQC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6UQC FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=FUC:ALPHA-L-FUCOSE'>FUC</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
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<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=6uqc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6uqc OCA], [http://pdbe.org/6uqc PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6uqc RCSB], [http://www.ebi.ac.uk/pdbsum/6uqc PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6uqc ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The development of antibody therapeutics relies on animal models that accurately recapitulate disease biology. Syngeneic mouse models are increasingly used with new molecules to capture the biology of complex cancers and disease states, and to provide insight into the role of the immune system. The establishment of syngeneic mouse models requires the ability to generate surrogate mouse counterparts to antibodies designed for humans. In the field of bispecific antibodies, there remains a dearth of technologies available to generate native IgG-like mouse bispecific antibodies. Thus, we engineered a simple co-expression system for one-step purification of intact mouse IgG1 and IgG2a bispecific antibodies from any antibody pair. We demonstrated proof of concept with CD3/CD20 bispecific antibodies, which highlighted both the quality and efficacy of materials generated by this technology.
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Authors:
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Design and characterization of mouse IgG1 and IgG2a bispecific antibodies for use in syngeneic models.,Wang F, Tsai JC, Davis JH, Chau B, Dong J, West SM, Hogan JM, Wheeler ML, Bee C, Morishige W, Cayton T, David-Brown D, Zhang C, Kozhich A, Sproul T, Dollinger G, Rajpal A, Strop P MAbs. 2020 Jan-Dec;12(1):1685350. doi: 10.1080/19420862.2019.1685350. PMID:31856660<ref>PMID:31856660</ref>
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Description:
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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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<div class="pdbe-citations 6uqc" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Davis, J H]]
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[[Category: Strop, P]]
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[[Category: Tsai, J C]]
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[[Category: Wang, F]]
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[[Category: West, S M]]
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[[Category: Bispecific]]
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[[Category: Electrostatic steering]]
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[[Category: Fc]]
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[[Category: Immune system]]

Revision as of 08:29, 1 January 2020

Mouse IgG2a Bispecific Fc

PDB ID 6uqc

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