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维生素D依赖型大鼠肾钙结合蛋白:放射免疫分析法的建立、组织分布及免疫学鉴定

Vitamin D-dependent rat renal calcium-binding protein: development of a radioimmunoassay, tissue distribution, and immunologic identification.

作者信息

Sonnenberg J, Pansini A R, Christakos S

出版信息

Endocrinology. 1984 Aug;115(2):640-8. doi: 10.1210/endo-115-2-640.

DOI:10.1210/endo-115-2-640
PMID:6378596
Abstract

A sensitive double antibody RIA has been developed for the 28,000 mol wt rat renal vitamin D-dependent calcium-binding protein. Using this assay, concentrations of calcium-binding protein (CaBP) as low as 30 ng can be measured. The assay is precise (intraassay variability, 5.0%) and reproductible (interassay variability, 8.2%). Measurements of renal CaBP by RIA showed a good correlation with measurements of CaBP by the chelex resin assay and by polyacrylamide gel analysis by densitometric tracing using a purified CaBP marker. The concentration of CaBP in the vitamin D-replete rat kidney is 7.3 +/- 1.0 (mean +/- SEM) micrograms/mg protein. In vitamin D-deficient rats the level of renal CaBP is 2.6 +/- 0.3 micrograms/mg protein. Tissue distribution of immunoreactive rat renal CaBP showed the highest concentration of CaBP in the rat cerebellum (38.3 +/- 5.1 micrograms/mg protein). Lower concentrations of immunoreactive CaBP were detected in several other rat tissues. No immunoreactive CaBP was detected in rat or human serum. In necropsy human kidney and cerebellum, high levels of immunoreactive CaBP were also detected (1.5 +/- 0.1 and 27.3 +/- 2.1 micrograms/mg protein, respectively). When extracts of rat kidney and brain and human cerebellum and kidney were assayed at several dilutions, immunodisplacement curves parallel to that of pure renal CaBP were observed, indicating immunochemical similarity. Fractionation of extracts of rat cerebellum, human kidney, and human cerebellum on Sephadex G-100 revealed immunoreactivity and calcium-binding activity in the 28,000 mol wt region similar to rat kidney.

摘要

已开发出一种用于检测分子量为28,000道尔顿的大鼠肾脏维生素D依赖性钙结合蛋白的灵敏双抗体放射免疫分析法(RIA)。使用该分析法,可检测低至30纳克的钙结合蛋白(CaBP)浓度。该分析法精确(批内变异率为5.0%)且可重复(批间变异率为8.2%)。通过RIA测定肾脏CaBP与通过螯合树脂分析法以及使用纯化的CaBP标记物进行光密度扫描的聚丙烯酰胺凝胶分析测定CaBP具有良好的相关性。维生素D充足的大鼠肾脏中CaBP的浓度为7.3±1.0(平均值±标准误)微克/毫克蛋白质。维生素D缺乏的大鼠肾脏中CaBP的水平为2.6±0.3微克/毫克蛋白质。免疫反应性大鼠肾脏CaBP的组织分布显示,大鼠小脑(38.3±5.1微克/毫克蛋白质)中CaBP的浓度最高。在其他几种大鼠组织中检测到较低浓度的免疫反应性CaBP。在大鼠或人血清中未检测到免疫反应性CaBP。在尸检的人肾脏和小脑中,也检测到高水平的免疫反应性CaBP(分别为1.5±0.1和27.3±2.1微克/毫克蛋白质)。当对大鼠肾脏和大脑以及人小脑和肾脏的提取物进行几种稀释度的检测时,观察到与纯肾脏CaBP平行的免疫置换曲线,表明免疫化学相似性。在葡聚糖凝胶G-100上对大鼠小脑、人肾脏和人小脑的提取物进行分级分离,发现在分子量为28,000道尔顿的区域具有与大鼠肾脏相似的免疫反应性和钙结合活性。

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