Abstract
A homogeneous glycoprotein was prepared by the improved tert-Boc solid-phase peptide synthesis of acid-labile sialylglycopeptide α-thioesters, sophisticated peptide-coupling reactions, and native chemical ligation. In their Communication on page 3567 ff., Y. Kajihara and co-workers report the chemical synthesis of a homogeneous erythropoietin glycoform bearing a complex-type biantennary disialyloligosaccharide. This approach will open a new avenue for the investigation of oligosaccharide function.
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