Refetoff S, Murata Y, Vassart G, Chandramouli V, Marshall J S
J Clin Endocrinol Metab. 1984 Aug;59(2):269-77. doi: 10.1210/jcem-59-2-269.
Antisera prepared by immunization of rabbits with human T4-binding globulin (TBG) contained two populations of antibodies: one directed against determinants of the native molecule, and the other directed against antigenic sites present only in denatured TBG. These two populations of antibodies were present in all nine antisera prepared in this or other laboratories that were tested. Exploiting this property of anti-TBG sera and using radioiodinated denatured TBG as a tracer, a RIA was developed which measures specifically denatured TBG in the presence of native TBG. The RIA for measuring denatured TBG used purified native TBG, which was denatured by reduction and pyridylethylation (RP-TBG) before labeling with 125I. Native TBG was measured using the same antiserum, but the 125I-labeled tracer was unmodified TBG. The sensitivity of the native TBG RIA was 0.25 ng purified native TBG. Equivalent amounts of native TBG in serum, desialylated TBG, and deglycosylated TBG produced superimposeable standard curves. The cross-reactivity with RP-TBG was less than 0.02%. The denatured TBG RIA had a sensitivity of 1 ng, and superimposeable curves were produced with equivalent concentrations of RP-TBG and heat-denatured native TBG. The cross-reactivity of 0.8% with native and deglycosylated TBG was, at least in part, due to denatured TBG in the purified preparations. The specificity of the two RIAs is due to the existence of distinct and exclusive antigenic determinants in native TBG and denatured TBG which are probably located on the surface of the tertiary structure and internally at the primary structure of the molecule, respectively. Heat and acid pH treatments of serum produced a progressive loss in immunoreactive native TBG, proportional to the loss of T4-binding capacity. A reciprocal and quantitative increase in denatured TBG, as measured in the denatured TBG RIA, was found. T4 partially protected the native TBG from denaturation. Denatured TBG was detected in sera from normal adults. The mean value was 6.05 +/- 2.25 (+/- SD) micrograms/dl (n = 11). Similar values were found in 8 pregnant women, 5 men with familial partial TBG deficiency, and 15 hypothyroid 7 hepatic, and 8 renal failure patients.(ABSTRACT TRUNCATED AT 400 WORDS)
用人甲状腺素结合球蛋白(TBG)免疫兔子制备的抗血清含有两类抗体:一类针对天然分子的决定簇,另一类针对仅存在于变性TBG中的抗原位点。在本实验室或其他实验室制备并检测的所有9份抗血清中均存在这两类抗体。利用抗TBG血清的这一特性,并以放射性碘化变性TBG作为示踪剂,开发了一种放射免疫分析法(RIA),可在天然TBG存在的情况下特异性检测变性TBG。用于检测变性TBG的RIA使用纯化的天然TBG,在用125I标记之前,通过还原和吡啶基乙基化使其变性(RP-TBG)。使用相同的抗血清检测天然TBG,但125I标记的示踪剂是未修饰的TBG。天然TBG RIA的灵敏度为0.25 ng纯化的天然TBG。血清、去唾液酸TBG和去糖基化TBG中等量的天然TBG产生可叠加的标准曲线。与RP-TBG的交叉反应性小于0.02%。变性TBG RIA的灵敏度为1 ng,等量的RP-TBG和热变性天然TBG产生可叠加的曲线。与天然和去糖基化TBG 0.8%的交叉反应性至少部分归因于纯化制剂中的变性TBG。这两种RIA的特异性归因于天然TBG和变性TBG中存在不同且互斥的抗原决定簇,它们可能分别位于分子三级结构的表面和一级结构的内部。血清经加热和酸性pH处理后,免疫反应性天然TBG逐渐丧失,与T4结合能力的丧失成比例。在用变性TBG RIA检测时,发现变性TBG呈反比且定量增加。T4部分保护天然TBG不发生变性。在正常成年人血清中检测到变性TBG。平均值为6.05±2.25(±标准差)μg/dl(n = 11)。在8名孕妇、5名患有家族性部分TBG缺乏症的男性以及15名甲状腺功能减退、7名肝病患者和8名肾衰竭患者中也发现了类似的值。(摘要截短至400字)