In this chapter we report on the characterization of linear antigenic sites of human chromogranin A (CgA), a useful tissue and serum marker for neuroendocrine tumours and a precursor of many biologically active peptides. The epitope mapping of CgA has been carried out by peptide microarrays on glass slides coated by a copolymer of N,N-dimethylacrylamide (DMA), N,N-acryloyloxysuccinimide (NAS) and [3-(methacryloyl-oxy) propyl] trimethoxysilyl (MAPS). The microarray support provided sufficient accessibility of the ligand, with no need for a spacer, as the polymer chains prevent interaction of immobilized peptides with substrate. In addition, the polymeric surface constitutes an aqueous micro-environment in which, despite peptide random orientation, linear epitopes are freely exposed. The results reported are in accordance with those obtained in conventional ELISA assays using biotinylated and non-biotinylated peptides.

Epitope mapping of human chromogranin A by peptide microarrays / M. Cretich, R. Longhi, A. Corti, F. Damin, G. Di Carlo, V. Sedini, M. Chiari (METHODS IN MOLECULAR BIOLOGY). - In: Peptide Microarrays : Methods and Protocols / [a cura di] M. Cretich, M. Chiari. - Prima edizione. - [s.l] : Humana Press, 2009. - ISBN 9781603273930. - pp. 221-232

Epitope mapping of human chromogranin A by peptide microarrays

G. Di Carlo;
2009

Abstract

In this chapter we report on the characterization of linear antigenic sites of human chromogranin A (CgA), a useful tissue and serum marker for neuroendocrine tumours and a precursor of many biologically active peptides. The epitope mapping of CgA has been carried out by peptide microarrays on glass slides coated by a copolymer of N,N-dimethylacrylamide (DMA), N,N-acryloyloxysuccinimide (NAS) and [3-(methacryloyl-oxy) propyl] trimethoxysilyl (MAPS). The microarray support provided sufficient accessibility of the ligand, with no need for a spacer, as the polymer chains prevent interaction of immobilized peptides with substrate. In addition, the polymeric surface constitutes an aqueous micro-environment in which, despite peptide random orientation, linear epitopes are freely exposed. The results reported are in accordance with those obtained in conventional ELISA assays using biotinylated and non-biotinylated peptides.
epitope mapping; human chromogranin A; peptide microarray; polymer coating; chromogranin A; epitope mapping; fluorescent dyes; humans; models, biological; peptides; protein array analysis; molecular biology; genetics; medicine (all)
Settore BIO/11 - Biologia Molecolare
2009
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/540716
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