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conference paper
A novel chemical approach to biotinylated glycosulfopeptides
2001
Peptides 2000, Proceedings of the European Peptide Symposium, 26th
A symposium report. A novel chem. approach for the synthesis of biotinylated glycosulfopeptides uses two different chemoselective ligation reactions in the presence of the sulfate moiety. The strategy was applied to the synthesis of a peptide sequence derived from the N-terminal region of the P-selectin glycoprotein ligand 1 (PSGL-1), a major ligand of the selectin family involved in cell-cell adhesion. [on SciFinder (R)]
Type
conference paper
Authors
Publication date
2001
Published in
Peptides 2000, Proceedings of the European Peptide Symposium, 26th
Start page
303
End page
304
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
February 9, 2006
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