8p6i
From Proteopedia
(Difference between revisions)
Line 7: | Line 7: | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8p6i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8p6i OCA], [https://pdbe.org/8p6i PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8p6i RCSB], [https://www.ebi.ac.uk/pdbsum/8p6i PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8p6i ProSAT]</span></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=8p6i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8p6i OCA], [https://pdbe.org/8p6i PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8p6i RCSB], [https://www.ebi.ac.uk/pdbsum/8p6i PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8p6i ProSAT]</span></td></tr> | ||
</table> | </table> | ||
- | == | + | <div style="background-color:#fffaf0;"> |
- | + | == Publication Abstract from PubMed == | |
- | + | Mucin 1 (MUC1) is a transmembrane mucin expressed at the apical surface of epithelial cells at mucosal surfaces. MUC1 has a barrier function against bacterial invasion and is well known for its aberrant expression and glycosylation in adenocarcinomas. The MUC1 extracellular domain contains a variable number of tandem repeats (VNTR) of 20 amino acids, which are heavily O-linked glycosylated. Monoclonal antibodies against the MUC1 VNTR are powerful research tools with applications in the diagnosis and treatment of MUC1-expressing cancers. Here, we report direct mass spectrometry-based sequencing of anti-MUC1 hybridoma-derived 139H2 IgG, enabling reverse-engineering of the functional recombinant monoclonal antibody. The crystal structure of the 139H2 Fab fragment in complex with the MUC1 epitope was solved, revealing the molecular basis of 139H2 binding specificity to MUC1 and its tolerance to O-glycosylation of the VNTR. The available sequence of 139H2 will allow further development of MUC1-related diagnostic, targeting, and treatment strategies. | |
- | + | ||
+ | Reverse-engineering the anti-MUC1 antibody 139H2 by mass spectrometry-based de novo sequencing.,Peng W, Giesbers KC, Siborova M, Beugelink JW, Pronker MF, Schulte D, Hilkens J, Janssen BJ, Strijbis K, Snijder J Life Sci Alliance. 2024 Mar 20;7(6):e202302366. doi: 10.26508/lsa.202302366. , Print 2024 Jun. PMID:38508723<ref>PMID:38508723</ref> | ||
+ | |||
+ | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
+ | </div> | ||
+ | <div class="pdbe-citations 8p6i" style="background-color:#fffaf0;"></div> | ||
== References == | == References == | ||
<references/> | <references/> |
Current revision
Crystal structure of the 139H2 Fab fragment bound to Muc1 peptide epitope
|