Crystal structure of a human MUC16 SEA domain reveals insight into the nature of the CA125 tumor marker. Issue 5 (25th January 2022)
- Record Type:
- Journal Article
- Title:
- Crystal structure of a human MUC16 SEA domain reveals insight into the nature of the CA125 tumor marker. Issue 5 (25th January 2022)
- Main Title:
- Crystal structure of a human MUC16 SEA domain reveals insight into the nature of the CA125 tumor marker
- Authors:
- White, Brandy
Patterson, Michelle
Karnwal, Saloni
Brooks, Cory L. - Other Names:
- Khare Sagar guestEditor.
Kozakov Dima guestEditor. - Abstract:
- Abstract: MUC16 is a membrane bound glycoprotein involved in the progression and metastasis of pancreatic and ovarian cancer. The protein is shed into the serum and the resulting cancer antigen 125 (CA125) can be detected by immunoassays. The CA125 epitope is used for monitoring ovarian cancer treatment progression, and has emerged as a potential target for antibody mediated immunotherapy. The extracellular tandem repeat domain of the protein is composed of repeating segments of heavily glycosylated sequence intermixed with homologous SEA (Sperm protein, Enterokinase and Agrin) domains. Here we report the purification and the first X‐ray structure of a human MUC16 SEA domain. The structure was solved by molecular replacement using a Rosetta generated structure as a search model. The SEA domain reacted with three different MUC16 therapeutic antibodies, confirming that the CA125 epitope is localized to the SEA domain. The structure revealed a canonical ferredoxin‐like fold, and contained a conserved disulfide bond. Analysis of the relative solvent accessibility of side chains within the SEA domain clarified the assignment of N‐linked and O‐linked glycosylation sites within the domain. A model of the glycosylated SEA domain revealed two major accessible faces, which likely represent the binding sites of CA125 specific antibodies. The results presented here will serve to accelerate future work to understand the functional role of MUC16 SEA domains and antibody recognition of theAbstract: MUC16 is a membrane bound glycoprotein involved in the progression and metastasis of pancreatic and ovarian cancer. The protein is shed into the serum and the resulting cancer antigen 125 (CA125) can be detected by immunoassays. The CA125 epitope is used for monitoring ovarian cancer treatment progression, and has emerged as a potential target for antibody mediated immunotherapy. The extracellular tandem repeat domain of the protein is composed of repeating segments of heavily glycosylated sequence intermixed with homologous SEA (Sperm protein, Enterokinase and Agrin) domains. Here we report the purification and the first X‐ray structure of a human MUC16 SEA domain. The structure was solved by molecular replacement using a Rosetta generated structure as a search model. The SEA domain reacted with three different MUC16 therapeutic antibodies, confirming that the CA125 epitope is localized to the SEA domain. The structure revealed a canonical ferredoxin‐like fold, and contained a conserved disulfide bond. Analysis of the relative solvent accessibility of side chains within the SEA domain clarified the assignment of N‐linked and O‐linked glycosylation sites within the domain. A model of the glycosylated SEA domain revealed two major accessible faces, which likely represent the binding sites of CA125 specific antibodies. The results presented here will serve to accelerate future work to understand the functional role of MUC16 SEA domains and antibody recognition of the CA125 epitope. … (more)
- Is Part Of:
- Proteins. Volume 90:Issue 5(2022)
- Journal:
- Proteins
- Issue:
- Volume 90:Issue 5(2022)
- Issue Display:
- Volume 90, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 90
- Issue:
- 5
- Issue Sort Value:
- 2022-0090-0005-0000
- Page Start:
- 1210
- Page End:
- 1218
- Publication Date:
- 2022-01-25
- Subjects:
- CA125 -- mucin -- ovarian cancer -- pancreatic cancer -- unknown function
Proteins -- Periodicals
Proteins -- Periodicals
572.6 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/prot.26303 ↗
- Languages:
- English
- ISSNs:
- 0887-3585
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.164000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26758.xml