Deftos L J
Department of Medicine, University of California, San Diego.
Clin Chem. 1992 Nov;38(11):2284-6.
We developed a two-site immunoradiometric assay (IRMA) of salmon calcitonin (SCT) that detects intact SCT(1-32) and not peptide fragments of the hormone. This was accomplished by using monoclonal antibodies prepared against the peptide fragments SCT(1-11) and SCT(11-32). Two antibodies with specificity for each of the peptides were purified from their respective ascites and evaluated in a two-site format wherein one of the antibodies was adsorbed to polystyrene beads and the other was radioiodinated. In this assay format, the antibody pair detected intact SCT(1-32) but did not react with either SCT(1-11) or SCT(11-32). The sensitivity of the assay could be increased by exchanging the antibodies with respect to bead adsorption and radioiodination. Furthermore, by increasing the incubation time and volume of incubation of sample with the polystyrene-bead-adsorbed antibody, the effective detection limit of the assay could be improved. This assay system can be used to detect intact SCT when the presence of fragments of the hormone might otherwise complicate interpretation of assay data.
我们开发了一种鲑鱼降钙素(SCT)的双位点免疫放射分析(IRMA),该方法可检测完整的SCT(1-32),而不是该激素的肽片段。这是通过使用针对肽片段SCT(1-11)和SCT(11-32)制备的单克隆抗体来实现的。从各自的腹水中纯化出对每种肽具有特异性的两种抗体,并以双位点形式进行评估,其中一种抗体吸附到聚苯乙烯珠上,另一种进行放射性碘化。在这种分析形式中,抗体对可检测完整的SCT(1-32),但不与SCT(1-11)或SCT(11-32)发生反应。通过交换抗体在珠吸附和放射性碘化方面的作用,可提高该分析的灵敏度。此外,通过增加样品与聚苯乙烯珠吸附抗体的孵育时间和孵育体积,可提高该分析的有效检测限。当激素片段的存在可能会使分析数据的解释复杂化时,该分析系统可用于检测完整的SCT。