The conformational space of the trisaccharide α-L-Fuc-(1 → 2)-β-D-Gal-(1 → 3)-β-D-GalNAc-1-OPr (2) and of its component disaccharide moieties α-L-Fuc-(1 → 2)-β-D-Gal-1-OMe (3) and β-D-Gal-(1 → 3)-β-D-GalNAc-1-OPr (4) was investigated with the aid of molecular-mechanics energy minimizations and molecular-dynamics simulations. These calculations suggested the occurrence of two conformations for each compound characterized by different Φ and ψ glycosidic angles. However, 1H-NMR investigation of D2O solutions of 2-4 indicated a sure preference for one of the two conformers with a contribution of the other one ranging from negligible to low.

Oligosaccharides Related to Tumor-Associate Antigens. Part 2. Conformational analysis of the trisaccharide α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GalpNAc, epitope structure recognized by the MBr1 antibody / L. Toma, P. Ciuffreda, D. Colombo, F. Ronchetti, L. Lay, L. Panza. - In: HELVETICA CHIMICA ACTA. - ISSN 0018-019X. - 77:3(1994), pp. 668-678. [10.1002/hlca.19940770310]

Oligosaccharides Related to Tumor-Associate Antigens. Part 2. Conformational analysis of the trisaccharide α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GalpNAc, epitope structure recognized by the MBr1 antibody

P. Ciuffreda
Secondo
;
D. Colombo;F. Ronchetti;L. Lay
Penultimo
;
1994

Abstract

The conformational space of the trisaccharide α-L-Fuc-(1 → 2)-β-D-Gal-(1 → 3)-β-D-GalNAc-1-OPr (2) and of its component disaccharide moieties α-L-Fuc-(1 → 2)-β-D-Gal-1-OMe (3) and β-D-Gal-(1 → 3)-β-D-GalNAc-1-OPr (4) was investigated with the aid of molecular-mechanics energy minimizations and molecular-dynamics simulations. These calculations suggested the occurrence of two conformations for each compound characterized by different Φ and ψ glycosidic angles. However, 1H-NMR investigation of D2O solutions of 2-4 indicated a sure preference for one of the two conformers with a contribution of the other one ranging from negligible to low.
Settore BIO/10 - Biochimica
1994
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/175789
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 10
social impact