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促甲状腺激素释放激素前体肽(赖氨酸-精氨酸-谷氨酰胺-组氨酸-脯氨酸-甘氨酸-精氨酸-精氨酸)的放射免疫测定法

Radioimmunoassay for thyrotropin-releasing hormone precursor peptide, Lys-Arg-Gln-His-Pro-Gly-Arg-Arg.

作者信息

Mitsuma T, Hirooka Y, Nogimori T, Senda Y

机构信息

Fourth Department of Internal Medicine, Aichi Medical University, Japan.

出版信息

Exp Clin Endocrinol. 1989 Apr;93(1):53-60. doi: 10.1055/s-0029-1210836.

Abstract

A radioimmunoassay for thyrotropin-releasing hormone (TRH) precursor peptide Lys-Arg-Gln-His-Pro-Gly-Arg-Arg (pro-TRH), has been developed. Anti-pro-TRH antibody was raised in rabbits immunized with a conjugate of synthetic pro-TRH analog, Cys-Lys-Arg-Gln-His-Pro-Gly-Arg-Arg-Cys (pCC10) to bovine serum albumin. This antibody did not cross-react with TRH, TRH-OH, His-Pro-diketopiperazine, neuropeptides, pituitary hormones and peptides which are included in prepro-TRH. Radioiodination of pCC 10 was performed by chloramin T method, followed by purification of radioiodinated material on Sephadex G-25 column. Pro-TRH was extracted from tissues, using 1.0 N acetic acid. The assay was performed with a double antibody system. The values are expressed as an equivalent of pCC 10. The dilution curves of acetic acid-extracts of rat hypothalamus and stomach in radioimmunoassay system were parallel to the standard curve. The recovery of tissue pro-TRH was 80%, the intra-assay and interassay variation was 5.2% and 8.9%, respectively. The elution profiles of acetic acid-extracts of the rat hypothalamus and stomach on Sephadex G-50 showed a single peak corresponding that of pCC 10. Immunoreactive pro-TRH was found in the rat brain, spinal cord, eye, stomach, intestine, pancreas and adrenal gland. These data suggest that this assay system is a suitable to measure pro-TRH in the tissues, and that pro-TRH is widely distributed in the rats.

摘要

已开发出一种用于促甲状腺激素释放激素(TRH)前体肽Lys-Arg-Gln-His-Pro-Gly-Arg-Arg(pro-TRH)的放射免疫分析方法。用合成的pro-TRH类似物Cys-Lys-Arg-Gln-His-Pro-Gly-Arg-Arg-Cys(pCC10)与牛血清白蛋白的偶联物免疫家兔,制备了抗pro-TRH抗体。该抗体与TRH、TRH-OH、His-Pro-二酮哌嗪、神经肽、垂体激素以及前pro-TRH中包含的肽均无交叉反应。采用氯胺T法对pCC 10进行放射性碘化,然后在Sephadex G-25柱上纯化放射性碘化物质。使用1.0 N乙酸从组织中提取pro-TRH。采用双抗体系统进行分析。结果以相当于pCC 10的量表示。放射免疫分析系统中大鼠下丘脑和胃的乙酸提取物的稀释曲线与标准曲线平行。组织pro-TRH的回收率为80%,批内变异和批间变异分别为5.2%和8.9%。大鼠下丘脑和胃的乙酸提取物在Sephadex G-50上的洗脱图谱显示出一个与pCC 10相对应的单峰。在大鼠脑、脊髓、眼、胃、肠、胰腺和肾上腺中发现了免疫反应性pro-TRH。这些数据表明该分析系统适用于测量组织中的pro-TRH,并且pro-TRH在大鼠体内广泛分布。

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