Andersson G, Lundgren E, Ekre H P
Research and Development Immunobiology, Kabi Biopharma, Stockholm, Sweden.
J Interferon Res. 1991 Feb;11(1):53-60. doi: 10.1089/jir.1991.11.53.
Four different mouse monoclonal antibodies to human interferon-alpha (IFN-alpha) were evaluated for application in quantitative and comparative analysis of natural IFN-alpha mixtures. Binding to IFN-alpha subtypes in solution revealed individual reactivity patterns. These patterns changed if the IFN-alpha molecules were immobilized either passively to a surface or bound by another antibody. Also, substitution of a single amino acid in IFN-alpha 2 affected the binding, apparently by altering the conformation. Isoelectric focusing of three natural IFN-alpha preparations from different sources, followed by immunoblotting, resulted in individual patterns with each of the four mAbs and also demonstrated variation in the composition of the IFN-alpha preparations. None of the mAbs was subtype specific, but by combining the different mAbs, and also applying polyclonal anti-human IFN-alpha antibodies, it was possible to design sensitive sandwich ELISAs with broad or more limited IFN-alpha subtype specificity.
对四种不同的抗人α干扰素(IFN-α)小鼠单克隆抗体进行了评估,以用于天然IFN-α混合物的定量和比较分析。这些抗体与溶液中的IFN-α亚型结合显示出各自的反应模式。如果IFN-α分子被动固定在表面或与另一种抗体结合,这些模式就会改变。此外,IFN-α 2中单个氨基酸的替换会影响结合,这显然是通过改变构象实现的。对来自不同来源的三种天然IFN-α制剂进行等电聚焦,然后进行免疫印迹,结果显示这四种单克隆抗体中的每一种都呈现出各自的模式,同时也证明了IFN-α制剂组成的差异。没有一种单克隆抗体具有亚型特异性,但通过将不同的单克隆抗体组合起来,并应用多克隆抗人IFN-α抗体,就有可能设计出具有广泛或更有限的IFN-α亚型特异性的灵敏夹心酶联免疫吸附测定法。