Sakata S, Kojima N, Horike S, Nakamura S, Kamikubo K, Komaki T, Miura K, Kondo Y, Haruna M, Itoh K
Nihon Naibunpi Gakkai Zasshi. 1983 Sep 20;59(9):1256-64. doi: 10.1507/endocrine1927.59.9_1256.
A very simple method for the evaluation of the interaction between thyroxine binding globulin (TBG) and thyroxine (T4) has been developed and evaluated in 6 healthy subjects and 5 pregnant women. Rabbit anti-human TBG antiserum was precipitated with 50% ammonium sulfate followed by passing a DEAE-cellulose column. Immunoglobulin G (IgG) fraction thus prepared was covalently attached on a Sepharose CL-4B and used as an immunoadsorbent of serum TBG. After treatment with charcoal to remove endogeneous thyroid hormones, 10 microliter of sera from 6 healthy subjects and 5 pregnant women were incubated with 125I-T4 and various concentrations of cold T4 followed by immunoadsorption with anti-TBG-Sepharose, and association constants (Ka) between TBG and T4 were calculated in each subject using Scatchard's plot. The Ka value thus obtained in 6 healthy subjects was 1.47 X 10(8) M-1 (SD = 0.24), and in 5 pregnant women it was 0.82 X 10(8) M-1 (SD = 0.21) which was significantly lower than that of healthy subjects (P less than 0.001). Our present method does not need purification of TBG from serum to investigate its functions, especially in relation to the binding with thyroid hormones. Also, only a very small amount (100 approximately 150 microliter) of serum is enough for the calculation of Ka between T4 and TBG. The whole procedure is very easy to perform and can be done in a relatively short time, and therefore we consider this method clinically relevant and useful.
已开发出一种评估甲状腺素结合球蛋白(TBG)与甲状腺素(T4)之间相互作用的非常简单的方法,并在6名健康受试者和5名孕妇中进行了评估。兔抗人TBG抗血清用50%硫酸铵沉淀,然后通过DEAE-纤维素柱。如此制备的免疫球蛋白G(IgG)级分共价连接到琼脂糖CL-4B上,并用作血清TBG的免疫吸附剂。在用活性炭处理以去除内源性甲状腺激素后,将6名健康受试者和5名孕妇的10微升血清与125I-T4和不同浓度的冷T4一起孵育,然后用抗TBG-琼脂糖进行免疫吸附,并使用Scatchard图计算每个受试者中TBG与T4之间的结合常数(Ka)。在6名健康受试者中获得的Ka值为1.47×10(8)M-1(标准差=0.24),在5名孕妇中为0.82×10(8)M-1(标准差=0.21),显著低于健康受试者(P<0.001)。我们目前的方法无需从血清中纯化TBG来研究其功能,特别是与甲状腺激素结合相关的功能。此外,仅需非常少量(约100至150微升)的血清就足以计算T4与TBG之间的Ka。整个过程非常易于操作,并且可以在相对较短的时间内完成,因此我们认为该方法具有临床相关性和实用性。