Abstract
A synthetic peptide corresponding to the human MUC2 tandem repeat domain containing 14 Thr residues was glycosylated in vitro using UDP-GalNAc and microsomal membranes of the colorectal cancer cell line, LS180. The products were fractionated by reverse phase HPLC, which gave seven glycopeptide fractions. Their molecular weights were estimated by matrix-assisted laser desorption/ionization mass spectrometry, the values obtained corresponding to glycopeptides containing from one to ten GalNAc residues. On solid phase radioimmunoassaying involving a monoclonal anti-Tn antibody (MLS128), it was found that the glycopeptides containing nine or ten GalNAc residues were strongly immunoreactive, whereas the glycopeptides containing less than six GalNAc residues were inactive, indicating that a cluster of GalNAc-Thr is essential for the Tn antigenicity.
Copyright 1998 Academic Press.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylgalactosamine / analysis
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Amino Acid Sequence
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Antibodies, Monoclonal / immunology
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Antibodies, Monoclonal / metabolism
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Antigens, Tumor-Associated, Carbohydrate / biosynthesis*
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Antigens, Tumor-Associated, Carbohydrate / immunology
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Colorectal Neoplasms / metabolism
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Glycopeptides / analysis
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Glycopeptides / immunology
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Glycosylation
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Humans
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Molecular Sequence Data
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Mucin-2
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Mucins / chemistry*
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N-Acetylgalactosaminyltransferases
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Peptide Fragments / chemical synthesis
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Peptide Fragments / metabolism
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Peptides
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Polypeptide N-acetylgalactosaminyltransferase
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Radioimmunoassay / methods
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Repetitive Sequences, Nucleic Acid / genetics*
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Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
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Tumor Cells, Cultured
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Uridine Diphosphate N-Acetylgalactosamine / metabolism
Substances
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Antibodies, Monoclonal
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Antigens, Tumor-Associated, Carbohydrate
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Glycopeptides
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MUC2 protein, human
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Mucin-2
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Mucins
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Peptide Fragments
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Peptides
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Tn antigen
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Uridine Diphosphate N-Acetylgalactosamine
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N-Acetylgalactosaminyltransferases
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Acetylgalactosamine