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Characterization of the oligosaccharide moiety of VIP receptor from the human pancreatic cell line BxPC-3
Authors:Catherine Fabre  Assou El Battari  Catherine Bellan  Eric Pasqualini  Jacques Marvaldi  Dominique Lombardo  Jos Luis
Institution:

* Institut de Chimie Biologique, CNRS URA 202, Université de Provence, 3 place Victor Hugo, 13331, Marseille cedex 3, France

Faculté de Médecine, INSERM U260, 27 Bd Jean Moulin, 13385, Marseille cedex 5, France

Abstract:The human pancreatic cell line BxPC-3 displays two classes of binding sites with high and low affinity for VIP. The order of potency of VIP-related peptides in inhibiting either 125I]VIP or 125I]N-AcPACAP27 binding and in stimulating cAMP production was typical of the human VIP receptor. By combining affinity labeling with glycosidase treatments, we have characterized the VIP receptor as a Mr = 68,200 glycoprotein, consisting of a Mr = 39,300 polypeptide core with at least three N-linked oligosaccharide chains. In addition, our results revealed the presence of a low amount of sialic acid residues in the carbohydrate moiety of receptor.
Keywords:Vasoactive intestinal peptide  VIP receptor  PACAP  Glycosylation  Carbohydrate chains  Pancreatic cancer
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