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一种从还原性寡糖构建具有抗原性和凝集素结合活性的新糖脂的改进方法。

Improved procedure for the construction of neoglycolipids having antigenic and lectin-binding activities, from reducing oligosaccharides.

作者信息

Stoll M S, Mizuochi T, Childs R A, Feizi T

机构信息

Section of Glycoconjugate Research, MRC Clinical Research Centre, Harrow, Middx., U.K.

出版信息

Biochem J. 1988 Dec 1;256(2):661-4. doi: 10.1042/bj2560661.

Abstract

Conditions have been established for the rapid and efficient conjugation of reducing oligosaccharides (di- to deca-saccharides) to dipalmitoyl phosphatidylethanolamine. The resulting neoglycolipids derived from several naturally occurring oligosaccharides and a series of N-linked high-mannose-type oligosaccharides released by hydrazinolysis from RNAase B showed specific and potent reactivities, as appropriate, with monoclonal antibodies to blood group Lewis(b), blood group A or a stage-specific embryonic (SSEA-1) antigen, or the lectin concanavalin A.

摘要

已经建立了将还原性低聚糖(二糖至十糖)与二棕榈酰磷脂酰乙醇胺快速高效缀合的条件。从几种天然存在的低聚糖以及通过肼解从核糖核酸酶B释放的一系列N-连接的高甘露糖型低聚糖衍生而来的新糖脂,分别与针对血型Lewis(b)、血型A或阶段特异性胚胎(SSEA-1)抗原的单克隆抗体或凝集素伴刀豆球蛋白A表现出特异性和强反应性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/049d/1135460/445fbc8d5fd9/biochemj00218-0334-a.jpg

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