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通过与含¹²⁵I的酰化剂结合将蛋白质标记至高比放射性。

The labelling of proteins to high specific radioactivities by conjugation to a 125I-containing acylating agent.

作者信息

Bolton A E, Hunter W M

出版信息

Biochem J. 1973 Jul;133(3):529-39. doi: 10.1042/bj1330529.

Abstract
  1. A new method is described for labelling proteins to high specific radioactivities with (125)I. The protein is treated with a (125)I-labelled acylating agent, iodinated 3-(4-hydroxyphenyl)propionic acid N-hydroxysuccinimide ester, which reacts with free amino groups in the protein molecule to attach the (125)I-labelled groups by amide bonds. 2. Three protein hormones have been labelled by this method, human growth hormone, human thyroid-stimulating hormone and human luteinizing hormone. Specific radioactivities of up to 170, 120 and 55muCi/mug respectively have been obtained for these hormones. 3. The immunoreactivity of these labelled hormones has been investigated by using a radioimmunoassay system specific for each hormone. These preparations have also been compared with and found to be equal or superior to labelled hormones prepared by chemical substitution of (125)I into tyrosine residues of the proteins by using the chloramine-t-oxidation procedure. 4. With some antisera the immunoreactivity of the antigen was diminished by the introduction of a single I atom into the tyrosyl groups, whereas antigen containing a single (125)I-labelled 3-(4-hydroxyphenyl)propionamide group showed the same immunoreactivity as the unmodified antigen.
摘要
  1. 描述了一种用(125)I 将蛋白质标记至高比放射性的新方法。蛋白质用(125)I 标记的酰化剂碘化 3-(4-羟苯基)丙酸 N-羟基琥珀酰亚胺酯处理,该酰化剂与蛋白质分子中的游离氨基反应,通过酰胺键连接(125)I 标记的基团。2. 用这种方法标记了三种蛋白质激素,即人生长激素、人促甲状腺激素和人促黄体生成激素。这些激素的比放射性分别高达 170、120 和 55μCi/μg。3. 通过使用针对每种激素的放射免疫分析系统研究了这些标记激素的免疫反应性。还将这些制剂与通过氯胺 -t 氧化程序将(125)I 化学取代到蛋白质酪氨酸残基制备的标记激素进行了比较,发现它们相等或更优。4. 对于一些抗血清,将单个 I 原子引入酪氨酸基团会降低抗原的免疫反应性,而含有单个(125)I 标记的 3-(4-羟苯基)丙酰胺基团的抗原显示出与未修饰抗原相同的免疫反应性。

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