Bailey G S
Department of Chemistry, University of Essex, Colchester, Essex, England.
Methods Mol Biol. 1984;1:301-10. doi: 10.1385/0-89603-062-8:301.
Immunodiffusion in gels encompasses a variety of techniques that are useful for the analysis of antigens and antibodies (1). The fundamental immunochemical principles behind their use are exactly the same as those that apply to antigen#x2013;antibody interactions in the liquid state. Thus an antigen will rapidly react its specific antibody to form a complex, the composition of which will depend on the nature, concentrations, and proportions of the initial reactants. As increasing amounts of a multivalent antigen are allowed to react with a fixed amount of antibody, precipitation occurs, in part because of extensive crosslinking between the reactant molecules. Initially the antibody is in excess and all of the added antigen is present in the form of an insoluble antigen#x2013;antibody aggregate. Addition of more antigen leads to the formation of more immune precipitate. However, a point is reached beyond which further addition of antigen produces an excess of antigen and leads to a reduction in the amount of the precipitate (see Fig. 1) because of the formation of soluble antigen#x2013;antibody complexes. Fig. 1. Variation in the amount of immune precipitate on addition of increasing amounts of antigen to a fixed amount of antibody.
凝胶免疫扩散涵盖多种技术,这些技术对于抗原和抗体的分析很有用(1)。其应用背后的基本免疫化学原理与适用于液态抗原 - 抗体相互作用的原理完全相同。因此,抗原会迅速与它的特异性抗体反应形成复合物,其组成将取决于初始反应物的性质、浓度和比例。当让越来越多的多价抗原与固定量的抗体反应时,就会发生沉淀,部分原因是反应物分子之间的广泛交联。最初抗体过量,所有添加的抗原都以不溶性抗原 - 抗体聚集体的形式存在。添加更多抗原会导致形成更多的免疫沉淀物。然而,会达到一个点,超过这个点进一步添加抗原会导致抗原过量,并由于可溶性抗原 - 抗体复合物的形成而导致沉淀物数量减少(见图1)。图1. 向固定量的抗体中添加越来越多的抗原时免疫沉淀物数量的变化。