Dorval G, Welsh K I, Wigzell H
J Immunol Methods. 1975 Jun;7(2-3):237-50. doi: 10.1016/0022-1759(75)90021-6.
Soluble protein A from Staphylococcus aureus does carry great promise as a marker for cellular surface determinants, due to its specific reaction with, and high affinity for, most subclasses of mammalian IgG. In this article we present the different parameters involved in a radioimmunoassay using 125-I-labelled protein A. Using such an approach the actual technical procedures involved are reported in detail together with tests for mammalian alloantigens, including HL-A in the human, H-2 in the mouse and AgB antigenic sites in the rat, as this presents an unique opportunity to compare them with already widely used assays for transplantation antigens. The different parameters of the assay are analysed in view of measuring with precision quantities of cell-surface IgG molecules, thereby allowing possible determinations of antigenic site numbers in a new and simplified manner.
金黄色葡萄球菌的可溶性蛋白A有望成为一种细胞表面决定簇的标志物,因为它能与大多数哺乳动物IgG亚类发生特异性反应且具有高亲和力。在本文中,我们介绍了使用125-I标记蛋白A的放射免疫分析所涉及的不同参数。采用这种方法,详细报告了实际的技术程序以及针对哺乳动物同种异体抗原的检测,包括人类的HL-A、小鼠的H-2和大鼠的AgB抗原位点,因为这提供了一个独特的机会将它们与已广泛用于移植抗原的检测方法进行比较。鉴于要精确测量细胞表面IgG分子的数量,对该分析的不同参数进行了分析,从而有可能以一种新的简化方式确定抗原位点的数量。