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Purification of subunit B of Shiga toxin using a synthetic trisaccharide-based affinity matrix.

作者信息

Pozsgay V, Trinh L, Shiloach J, Robbins J B, Donohue-Rolfe A, Calderwood S B

机构信息

Laboratory of Developmental and Molecular Immunity, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Bioconjug Chem. 1996 Jan-Feb;7(1):45-55. doi: 10.1021/bc9500711.

Abstract

The blood group P1 antigenic trisaccharide (3), which is the receptor-binding ligand of Shiga-like toxins, is synthesized in a spacer-equipped form (32) from 2-(trimethylsilyl)ethyl glucoside 5 and the 1-thiogalactoside building blocks 10 and 22 in a stereocontrolled, stepwise fashion. Covalent attachment of 32 to hydrazine group-containing agarose gel by reductive amination provided the P1 trisaccharide-containing affinity sorbent which was used for preparative scale isolation of subunit B of Shiga toxin.

摘要

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