Stoll M S, Mizuochi T, Childs R A, Feizi T
Section of Glycoconjugate Research, MRC Clinical Research Centre, Harrow, Middx., U.K.
Biochem J. 1988 Dec 1;256(2):661-4. doi: 10.1042/bj2560661.
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.
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。