We report the design, synthesis and immunological evaluation of a series of glycopeptide analogues of the previously described antigenic probe CSF114(Glc), with the aim of understanding the importance of N-glycosylation on Asn residue in multiple sclerosis antibody recognition. The glucopeptide, characterized by a beta-turn conformation which is fundamental for a correct presentation of the epitope, has been modified by introducing various natural glycoamino acids in position 7. The new glycopeptides were evaluated by measuring the IgG and IgM antibody titre in MS patients' and normal blood donors' sera. Moreover, we achieved the efficient synthetic strategy of new Asn derivative bearing N-acetylneuraminic acid (Neu5Ac), linked by an N-glycosidic bond, on the side chain of the Asn residue orthogonally protected for Fmoc/tBu SPPS. (c) 2010 Wiley Periodicals, Inc. Biopolymers (Pept Sci), 2010.
Post-translationally modified peptides efficiently mimicking neo-antigens: A challenge for theragnostics of autoimmune diseases / Nuti, F;Peroni, E; Real-Fernández, F;Bonache, MA;Chevalier-Isaad, L;Chelli, M;Lubin-Germain, N;Uziel, J;Rovero, P;Lolli, F; Papini, AM. - In: BIOPOLYMERS. - ISSN 0006-3525. - ELETTRONICO. - 94:(2010), pp. 791-799. [10.1002/bip.21456]
Post-translationally modified peptides efficiently mimicking neo-antigens: A challenge for theragnostics of autoimmune diseases.
NUTI, FRANCESCA;ROVERO, PAOLO;LOLLI, FRANCESCO;PAPINI, ANNA MARIA
2010
Abstract
We report the design, synthesis and immunological evaluation of a series of glycopeptide analogues of the previously described antigenic probe CSF114(Glc), with the aim of understanding the importance of N-glycosylation on Asn residue in multiple sclerosis antibody recognition. The glucopeptide, characterized by a beta-turn conformation which is fundamental for a correct presentation of the epitope, has been modified by introducing various natural glycoamino acids in position 7. The new glycopeptides were evaluated by measuring the IgG and IgM antibody titre in MS patients' and normal blood donors' sera. Moreover, we achieved the efficient synthetic strategy of new Asn derivative bearing N-acetylneuraminic acid (Neu5Ac), linked by an N-glycosidic bond, on the side chain of the Asn residue orthogonally protected for Fmoc/tBu SPPS. (c) 2010 Wiley Periodicals, Inc. Biopolymers (Pept Sci), 2010.File | Dimensione | Formato | |
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