Klieber R, Panmoung W, Berger P, Wick G
Forschungsstelle für Immunendokrinologie der Osterreichischen Akademie der Wissenschaften, Universität, Innsbruck.
Wien Klin Wochenschr. 1990 May 11;102(10):283-9.
Using a panel of monoclonal antibodies (MCA) to human chorionic gonadotropin (hCG) and its alpha and beta subunits and additional MCA to the non-assembled, free alpha and beta chains which were produced in the course of the present experiments, it was possible to extend the previously established epitope map of hCG. Two MCAs turned out to be specific for the free alpha chain of the glycoprotein hormones (GPH) and, thus, did not react with holo hCG. Two other MCA recognized two epitopes (beta 6 and beta 7) on the free form of the hCG beta only. Again, no holo hormone cross-reaction was observed. Whereas previously only nine antigenic hCG determinants (3 alpha, 4 beta, 2c) had been demonstrated, it was now possible to distinguish fourteen epitopes (5 alpha, 5 beta, 4c). In addition, epitope maps were established for the non-assembled, free subunits of hCG. These comprise six epitopes on the alpha chain (alpha 1- alpha 6) and seven on the beta chain (beta 1- beta 7). Both so far generally accepted premises of Judith Vaitukaitis, claiming the beta chain of the GPH to be immunologically species-specific, the beta chain to be immunologically hormone-specific, were clearly disproven by demonstrating inter- and intra-species cross-reaction of some MCA. Based on the immunological topography of the holo hCG molecule and its free subunits, highly specific and sensitive immuno-enzymometric assays (IEMA) with predictable specificities were designed, measuring either non-assembled subunits alone or in combination with the intact hormones.
利用一组针对人绒毛膜促性腺激素(hCG)及其α和β亚基的单克隆抗体(MCA),以及针对在本实验过程中产生的未组装的游离α和β链的其他MCA,有可能扩展先前建立的hCG表位图谱。结果发现,两种MCA对糖蛋白激素(GPH)的游离α链具有特异性,因此不与完整的hCG发生反应。另外两种MCA仅识别hCG β游离形式上的两个表位(β6和β7)。同样,未观察到与完整激素的交叉反应。以前仅证实了九个抗原性hCG决定簇(3个α、4个β、2个c),现在有可能区分出14个表位(5个α、5个β、4个c)。此外,还建立了hCG未组装的游离亚基的表位图谱。这些包括α链上的六个表位(α1-α6)和β链上的七个表位(β1-β7)。朱迪思·韦图凯蒂斯(Judith Vaitukaitis)目前普遍接受的两个前提,即声称GPH的β链在免疫上具有种属特异性,β链在免疫上具有激素特异性,通过证明一些MCA的种间和种内交叉反应而被明确否定。基于完整hCG分子及其游离亚基的免疫拓扑结构,设计了具有可预测特异性的高度特异性和灵敏的免疫酶联分析(IEMA),可单独测量未组装的亚基或与完整激素一起测量。