On-line post-capillary affinity detection of immunoglobulin G subclasses and monoclonal antibody variants for capillary electrophoresis

被引:12
|
作者
Kelly, JA
Lee, CS
机构
[1] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[2] Iowa State Univ, US DOE, Ames Lab, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
affinity detection; detection; electrophoresis; protein heterogeneity; immunoglobulins; monoclonal antibodies; proteins;
D O I
10.1016/S0021-9673(97)00760-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human immunoglobulin G (IgG) subclasses each play a unique role in an immune response to foreign antigens. Three of the human IgG subclasses have distinct electrophoretic mobilities and are resolved by capillary zone electrophoresis (CZE). A post-capillary reactor is constructed to allow on-line addition of fragment B (of protein A)-fluorescein to form affinity complexes with separated IgG subclasses. Post-capillary affinity detection provides selective identification of human IgG subclasses and illustrates the effect of affinity binding constant on detection sensitivity. Additionally, post-capillary affinity detection for CZE facilitates rapid and selective heterogeneity analysis of mouse monoclonal anti-(human-alpha(1)-antitrypsin) and anti-human follicle stimulating hormone in complex sample matrices. A constant mobility difference is observed between the antibody isoforms, likely the result of charge heterogeneity due to deamination, degradation or variation in sialic acid content. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:207 / 214
页数:8
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