7U9J

Crystal structure of Mesothelin-207 fragment

Summary for 7U9J

• Entry DOI: 10.2210/pdb7u9j/pdb
• Descriptor: Isoform 3 of Mesothelin, SULFATE ION, GLYCEROL, ... (4 entities in total)
• Functional Keywords: mesothelin, cell adhesion
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 2
• Total formula weight: 49536.38

Authors

Zhan, J.,Esser, L.,Lin, D.,Tang, W.K.,Xia, D. (deposition date: 2022-03-10, release date: 2023-02-01, Last modification date: 2024-11-06)

Primary citation

Zhan, J.,Lin, D.,Watson, N.,Esser, L.,Tang, W.K.,Zhang, A.,Liu, X.,Hassan, R.,Gleinich, A.,Shajahan, A.,Azadi, P.,Pastan, I.,Xia, D.
Structures of Cancer Antigen Mesothelin and Its Complexes with Therapeutic Antibodies.
Cancer Res Commun, 3:175-191, 2023

PubMed Abstract: The tumor-associated antigen mesothelin is expressed at high levels on the cell surface of many human cancers, while its expression in normal tissues is limited. The binding of mesothelin to the tumor-associated cancer antigen 125 (CA-125) can lead to heterotypic cell adhesion and tumor metastasis within the pleural and peritoneal cavities. Immunotherapeutic strategies targeting mesothelin are being intensively investigated. Here, we report the crystal structures of mesothelin that reveal a compact, right-handed solenoid consisting of 24 short helices and connecting loops. These helices form a nine-layered spiral coil that resembles ARM/HEAT family proteins. Glycan attachments have been identified in the structure for all three predicted N-glycosylation sites and confirmed with samples from cell culture and patient ascites. The structures of full-length mesothelin and its complex with the Fab of MORAb-009 reveal the interaction of the antibody with the complete epitope, which has not been reported previously. The N-terminal half of mesothelin is conformationally rigid, suitable for eliciting specific antibodies, whereas its C-terminal portion is more flexible. The structure of the C-terminal shedding-resistant fragment of mesothelin complexed with a mAb 15B6 displays an extended linear epitope and helps explain the protection afforded by the antibody for the shedding sites.

PubMed: 36968141
DOI: 10.1158/2767-9764.CRC-22-0306

Experimental method

X-RAY DIFFRACTION (2.09 Å)