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Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.

The anti-breast carcinoma monoclonal antibody (MAb), NCRC-11 defines a polymorphic epithelial mucin (PEM) which is elevated in the circulation of advanced breast carcinoma patients. Here we describe the purification and partial characterisation of this component from patients' sera and its use...

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Autores principales: O'Sullivan, C., Price, M. R., Baldwin, R. W.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971673/
https://www.ncbi.nlm.nih.gov/pubmed/1695521
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author O'Sullivan, C.
Price, M. R.
Baldwin, R. W.
author_facet O'Sullivan, C.
Price, M. R.
Baldwin, R. W.
author_sort O'Sullivan, C.
collection PubMed
description The anti-breast carcinoma monoclonal antibody (MAb), NCRC-11 defines a polymorphic epithelial mucin (PEM) which is elevated in the circulation of advanced breast carcinoma patients. Here we describe the purification and partial characterisation of this component from patients' sera and its use in the production of a second generation MAb, C568 (IgM). Pooled sera was fractionated by immunoaffinity and size-exclusion chromatography and the purity of preparations assessed by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and immunoblotting. Serum-derived PEM shows a similar pattern of electrophoretic mobility to PEM isolated from primary breast tumour tissue and migrates as several bands in 4% SDS polyacrylamide gels (Mr greater than 400,000). The epitope expression of PEMs isolated from either source is also similar, with both bearing topographically distinct determinants for several anti-mucin MAbs. The immunoreactivities of antibodies C568 and NCRC-11 were unaffected by boiling, reduction and alkylation, or by enzyme desialylation of PEM. Periodate oxidation and proteolytic digestion have suggested that the antigenic determinant for C568 is carbohydrate in nature whilst that of NCRC-11 is peptidic. In accord with the mucinous nature of the molecule, serum-derived PEM is susceptible to reductive beta-elimination, elutes in the void volume of a Sepharose CL-4B column and has a buoyant density of 1.45 g ml-1. IMAGES:
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spelling pubmed-19716732009-09-10 Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation. O'Sullivan, C. Price, M. R. Baldwin, R. W. Br J Cancer Research Article The anti-breast carcinoma monoclonal antibody (MAb), NCRC-11 defines a polymorphic epithelial mucin (PEM) which is elevated in the circulation of advanced breast carcinoma patients. Here we describe the purification and partial characterisation of this component from patients' sera and its use in the production of a second generation MAb, C568 (IgM). Pooled sera was fractionated by immunoaffinity and size-exclusion chromatography and the purity of preparations assessed by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and immunoblotting. Serum-derived PEM shows a similar pattern of electrophoretic mobility to PEM isolated from primary breast tumour tissue and migrates as several bands in 4% SDS polyacrylamide gels (Mr greater than 400,000). The epitope expression of PEMs isolated from either source is also similar, with both bearing topographically distinct determinants for several anti-mucin MAbs. The immunoreactivities of antibodies C568 and NCRC-11 were unaffected by boiling, reduction and alkylation, or by enzyme desialylation of PEM. Periodate oxidation and proteolytic digestion have suggested that the antigenic determinant for C568 is carbohydrate in nature whilst that of NCRC-11 is peptidic. In accord with the mucinous nature of the molecule, serum-derived PEM is susceptible to reductive beta-elimination, elutes in the void volume of a Sepharose CL-4B column and has a buoyant density of 1.45 g ml-1. IMAGES: Nature Publishing Group 1990-06 /pmc/articles/PMC1971673/ /pubmed/1695521 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
O'Sullivan, C.
Price, M. R.
Baldwin, R. W.
Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
title Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
title_full Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
title_fullStr Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
title_full_unstemmed Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
title_short Polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
title_sort polymorphic epithelial mucin from the sera of advanced breast cancer patients--isolation and partial characterisation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971673/
https://www.ncbi.nlm.nih.gov/pubmed/1695521
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