Birshtein B K, Preud'homme J L, Scharff M D
Proc Natl Acad Sci U S A. 1974 Sep;71(9):3478-82. doi: 10.1073/pnas.71.9.3478.
After mutagenesis of cultured mouse myeloma cells with ICR 191 or Melphalan, variant clones were isolated that synthesized immunoglobulin heavy chains shorter than those produced by the parent. These variants fell into two phenotypes, based on the size, serology, and pattern of assembly of the heavy chain. Variant chains of both types no longer reacted with antisera directed either against the Fc (C-terminal half of the heavy chains) or subclass-specific IgG(2b) determinants. Comparative ion exchange chromatography of tryptic-chymotryptic peptides confirmed that the variant heavy chains differed structurally from those of the parent and from each other. A conversion from one phenotype to the other has been observed.
用ICR 191或美法仑对培养的小鼠骨髓瘤细胞进行诱变后,分离出了变异克隆,这些克隆合成的免疫球蛋白重链比亲本产生的重链短。根据重链的大小、血清学和组装模式,这些变异体分为两种表型。两种类型的变异链均不再与针对Fc(重链的C端一半)或亚类特异性IgG(2b)决定簇的抗血清发生反应。胰蛋白酶-糜蛋白酶肽段的比较离子交换色谱分析证实,变异重链在结构上与亲本重链不同,彼此之间也不同。已经观察到从一种表型向另一种表型的转变。