Menini T, Gugliucci A, Stahl A J
Departement d'Immunologie, Immunopharmacologie et Pathologie, Faculté de Pharmacie, Université Louis Pasteur, Illkirch, France.
Clin Chim Acta. 1992 Dec 31;213(1-3):23-35. doi: 10.1016/0009-8981(92)90218-f.
A four step purification procedure for polyclonal human serum IgM was elaborated, including ultracentrifugation, ammonium sulfate and polyethyleneglycol precipitations and diffusion-exclusion gel chromatography. IgM was glycated in vitro both in the presence of [14C]glucose and with unlabeled glucose. Influence of incubation time up to 10 days and of glucose concentration between 10 and 60 mmol/l were studied. With 10 mmol/l glucose, a molar ratio glucose/IgM of 5.7 was attained in 10 days. Increase of glucose concentration up to 60 mmol/l led to a molar ratio of 16.0. Both basal and in vitro glycation were evaluated by 3H-labeling by gel filtration and Concanavalin A-Sepharose chromatographies. Glycation occurs mainly on the heavy chains (> 85%), particularly on the Fd region.
阐述了一种用于纯化多克隆人血清IgM的四步程序,包括超速离心、硫酸铵和聚乙二醇沉淀以及排阻凝胶色谱法。IgM在[14C]葡萄糖存在下和未标记葡萄糖的情况下进行体外糖基化。研究了长达10天的孵育时间以及10至60 mmol/l的葡萄糖浓度的影响。在10 mmol/l葡萄糖条件下,10天内葡萄糖/IgM的摩尔比达到5.7。葡萄糖浓度增加至60 mmol/l导致摩尔比为16.0。通过凝胶过滤和伴刀豆球蛋白A-琼脂糖色谱法的3H标记评估基础糖基化和体外糖基化。糖基化主要发生在重链上(>85%),特别是在Fd区域。