Beck B N, Pease L R, Bell M P, Buerstedde J M, Nilson A E, Schlauder G G, McKean D J
J Exp Med. 1987 Aug 1;166(2):433-43. doi: 10.1084/jem.166.2.433.
We have produced a series of in vitro serologically selected cell lines that express mutant I-Ak molecules. In this report we describe the DNA sequence analysis of the Ak beta gene of four cell lines that express serologically altered Ak beta polypeptides in association with wild-type Ak alpha polypeptides. Each of the major serologic epitopes on the Ak beta polypeptide has been altered in one or more of the four mutants. In addition, the four mutants exhibit a broad spectrum of functional defects when used to stimulate a panel of T hybridomas of various specificities. The DNA sequence analysis revealed that each mutant had sustained a single nucleotide substitution resulting in a single amino acid substitution. All four independent substitutions occurred within or near the third of the four variable regions defined in the beta 1 domain of the A beta polypeptide by allelic comparisons. These data strongly suggest that the third variable region is the major determinant of alloantigenicity on the Ak beta polypeptide.
我们已经构建了一系列表达突变I-Ak分子的体外血清学选择细胞系。在本报告中,我们描述了四个细胞系的Ak β基因的DNA序列分析,这些细胞系表达与野生型Ak α多肽相关的血清学改变的Ak β多肽。Ak β多肽上的每个主要血清学表位在四个突变体中的一个或多个中发生了改变。此外,当用于刺激一组具有各种特异性的T杂交瘤时,这四个突变体表现出广泛的功能缺陷。DNA序列分析表明,每个突变体都发生了单个核苷酸取代,导致单个氨基酸取代。通过等位基因比较,所有四个独立取代都发生在Aβ多肽β1结构域中定义的四个可变区的第三个可变区内或附近。这些数据强烈表明,第三个可变区是Ak β多肽上同种抗原性的主要决定因素。