Efficient synthesis of a sialyl T-antigen-linked glycopeptide by the chemoenzymatic method

12Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A sialyl T-antigen-linked tetrapeptide was prepared by the combined method of chemical synthesis and enzymatic synthesis. The GalNAc-linked peptide was first obtained by using a commercial peptide synthesizer, and then a galactose residue was attached with β-(1→3)-linkage by transglycosylating with a recombinant β-galactosidase from Bacillus circulans. The sialic acid residue was then combined by α-(2→3)-linkage with sialytransferase from rat liver. © 2000, Taylor & Francis Group, LLC. All rights reserved.

Cite

CITATION STYLE

APA

Ajisaka, K., & Miyasato, M. (2000). Efficient synthesis of a sialyl T-antigen-linked glycopeptide by the chemoenzymatic method. Bioscience, Biotechnology and Biochemistry, 64(8), 1743–1746. https://doi.org/10.1271/bbb.64.1743

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free