4.7 Article

Multivalent Galacto-trehaloses: Design, Synthesis, and Biological Evaluation under the Concept of Carbohydrate Modules

Journal

BIOMACROMOLECULES
Volume 10, Issue 7, Pages 1846-1853

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bm900283x

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Funding

  1. 21st Century COE program Nature-Guided Materials Processing of the Ministry of Education, Culture, Sport, Science and Technology (MEXT) of Japanese Government
  2. special Coordination Funds for Promoting Science and Technology from the MEXT of Japan

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Galacto-trehalose (GT) is a novel class of 1,1'-linked nonreducing disaccharide having an alpha-galactoside epitope. In this study, a pair of alpha,alpha- and alpha,beta-GT isomers were prepared in one pot with our alpha-glycosylation method, converted into vinyl monomers and then subjected to radical copolymerization with a second sugar (4-acrylamidophemyl beta-Glc or beta-GlcNAc) in the presence of acrylamide. The derived glycopolymers were assayed with alpha-galactoside-specific proteins (BSI-B-4 lectin and Shiga toxin-1) to show the results that both alpha,alpha- and alpha,beta-isomers are recognized by these carbohydrate-binding proteins more strongly in forms of the GT polymers. Moreover, the glycopolymer carrying both alpha,alpha-GT and beta-GlcNAc along the polymer chain showed an integrated detoxifying activity to the E. coli toxin as the result of a module effect of the second sugar.

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