Javid J, Yingling W
J Clin Invest. 1968 Oct;47(10):2297-304. doi: 10.1172/JCI105915.
Using a radioimmunoassay method in conjunction with double diffusion studies, we characterized the antigenic determinants of the three Hp Bellevue phenotypes. An antigenic model based on these data indicates that each phenotype comprises a heterogeneous group of proteins with properties depending on their content of normal (hpbeta) and of mutant (hpbeta-Bellevue) chains of haptoglobin. The loss of the hemoglobin binding capacity and of a specific Hb-sensitive antigenic determinant is a consequence of the structural alteration in hpbeta-Bellevue and is expressed to various extents by the populations of proteins containing this chain. It is suggested that those molecules with a preponderance of mutant beta-chains are without significant hemoglobin binding capacity and are degraded more slowly in vivo than the ones capable of hemoglobin binding.
我们采用放射免疫测定法并结合双向扩散研究,对三种血红蛋白 Bellevue 表型的抗原决定簇进行了表征。基于这些数据的抗原模型表明,每种表型都包含一组异质性蛋白质,其特性取决于它们所含触珠蛋白正常链(hpβ)和突变链(hpβ - Bellevue)的含量。血红蛋白结合能力和特定 Hb 敏感抗原决定簇的丧失是 hpβ - Bellevue 结构改变的结果,并且在含有该链的蛋白质群体中以不同程度表现出来。有人提出,那些以突变β链为主的分子没有显著的血红蛋白结合能力,并且在体内比能够结合血红蛋白的分子降解得更慢。