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Synthesis of a water-soluble serine-based neoglycolipid which can be covalently linked to solid phases.

作者信息

Elofsson M, Broddefalk J, Ekberg T, Kihlberg J

机构信息

Chemical Center, University of Lund, Sweden.

出版信息

Carbohydr Res. 1994 May 20;258:123-33. doi: 10.1016/0008-6215(94)84080-6.

DOI:10.1016/0008-6215(94)84080-6
PMID:8039173
Abstract

N alpha-Fmoc-serine pentafluorophenyl ester was glycosylated with perbenzoylated lactosyl bromide. The resulting product was coupled to a resin functionalized with 6-aminohexanoic acid and then N alpha-acylated to give a serine-based analogue of lactosylceramide. The water-soluble neoglycolipid was covalently linked to microtiter plates via its carboxyl group and was recognized by a lactose-binding lectin in an ELISA.

摘要

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