8cr9

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Current revision (07:27, 22 November 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8cr9 is ON HOLD until 2025-03-08
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==Cryo-EM structure of PcrV/Fab(30-B8)==
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<StructureSection load='8cr9' size='340' side='right'caption='[[8cr9]], [[Resolution|resolution]] 4.20&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8cr9]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Pseudomonas_aeruginosa Pseudomonas aeruginosa]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8CR9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8CR9 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">Electron Microscopy, [[Resolution|Resolution]] 4.2&#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=8cr9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cr9 OCA], [https://pdbe.org/8cr9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cr9 RCSB], [https://www.ebi.ac.uk/pdbsum/8cr9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cr9 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides.[https://www.uniprot.org/uniprot/G3XD49_PSEAE G3XD49_PSEAE]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Drug-resistant Pseudomonas aeruginosa (PA) poses an emerging threat to human health with urgent need for alternative therapeutic approaches. Here, we deciphered the B cell and antibody response to the virulence-associated type III secretion system (T3SS) in a cohort of patients chronically infected with PA. Single-cell analytics revealed a diverse B cell receptor repertoire directed against the T3SS needle-tip protein PcrV, enabling the production of monoclonal antibodies (mAbs) abrogating T3SS-mediated cytotoxicity. Mechanistic studies involving cryoelectron microscopy identified a surface-exposed C-terminal PcrV epitope as the target of highly neutralizing mAbs with broad activity against drug-resistant PA isolates. These anti-PcrV mAbs were as effective as treatment with conventional antibiotics in vivo. Our study reveals that chronically infected patients represent a source of neutralizing antibodies, which can be exploited as therapeutics against PA.
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Authors: Yuan, B., Simonis, A., Marlovits, T.C.
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Discovery of highly neutralizing human antibodies targeting Pseudomonas aeruginosa.,Simonis A, Kreer C, Albus A, Rox K, Yuan B, Holzmann D, Wilms JA, Zuber S, Kottege L, Winter S, Meyer M, Schmitt K, Gruell H, Theobald SJ, Hellmann AM, Meyer C, Ercanoglu MS, Cramer N, Munder A, Hallek M, Fatkenheuer G, Koch M, Seifert H, Rietschel E, Marlovits TC, van Koningsbruggen-Rietschel S, Klein F, Rybniker J Cell. 2023 Nov 9;186(23):5098-5113.e19. doi: 10.1016/j.cell.2023.10.002. Epub , 2023 Nov 1. PMID:37918395<ref>PMID:37918395</ref>
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Description: Cryo-EM structure of PcrV/Fab(30-B8)
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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: Yuan, B]]
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<div class="pdbe-citations 8cr9" style="background-color:#fffaf0;"></div>
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[[Category: Simonis, A]]
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== References ==
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[[Category: Marlovits, T.C]]
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<references/>
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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: Pseudomonas aeruginosa]]
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[[Category: Marlovits TC]]
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[[Category: Simonis A]]
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[[Category: Yuan B]]

Current revision

Cryo-EM structure of PcrV/Fab(30-B8)

PDB ID 8cr9

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