Blind E, Schmidt-Gayk H, Armbruster F P, Stadler A
Clin Chem. 1987 Aug;33(8):1376-81.
This is an immunoradiometric assay of intact human parathyrin, hPTH(1-84). One antibody, directed against the N-terminal part of the hormone, was produced in goats and conjugated covalently to cellulose particles. hPTH(1-84) and the N-terminal fragments were extracted from EDTA-treated plasma by these particles and thus concentrated. Another antibody, against synthetic hPTH(53-84), was raised in rabbits; this bound to the C-terminal part of the hormone. The final step was labeling the second free binding site of this antibody with 125I-labeled Tyr52-hPTH(53-84) and measuring the bound radioactivity. This assay can detect intact PTH in concentrations as low as 0.6 pmol/L (1.2 X 10(-16) mol per tube). The assay did not cross react with hPTH(1-34), hPTH(1-44), hPTH(28-48), hPTH(39-84), hPTH(44-68), or hPTH(53-84) in concentrations up to 6400 pmol/L. In 60 normal subjects, hPTH(1-84) concentrations ranged from 1.9 to 6.8 pmol/L; in 32 patients with primary hyperparathyroidism, from 7.0 to 80 pmol/L. The hormone was not detected in four patients with hypoparathyroidism.
这是一种针对完整人甲状旁腺素hPTH(1 - 84)的免疫放射分析方法。一种针对该激素N端部分的抗体由山羊产生,并与纤维素颗粒共价结合。hPTH(1 - 84)和N端片段通过这些颗粒从经乙二胺四乙酸(EDTA)处理的血浆中提取出来并得以浓缩。另一种针对合成的hPTH(53 - 84)的抗体由兔子产生;它与该激素的C端部分结合。最后一步是用125I标记的Tyr52 - hPTH(53 - 84)标记该抗体的第二个游离结合位点,并测量结合的放射性。该分析方法能够检测低至0.6 pmol/L(每管1.2×10(-16)摩尔)浓度的完整甲状旁腺素。该分析方法与浓度高达6400 pmol/L的hPTH(1 - 34)、hPTH(1 - 44)、hPTH(28 - 48)、hPTH(39 - 84)、hPTH(44 - 68)或hPTH(53 - 84)均无交叉反应。在60名正常受试者中,hPTH(1 - 84)浓度范围为1.9至6.8 pmol/L;在32名原发性甲状旁腺功能亢进患者中,浓度范围为7.0至80 pmol/L。在4名甲状旁腺功能减退患者中未检测到该激素。