Krangel M S, Pious D, Strominger J L
J Immunol. 1984 Jun;132(6):2984-91.
HLA-A2 antigen mutants were obtained previously from the B lymphoblastoid cell line T5-1 by mutagenesis followed by immunoselection. Here we present biochemical studies of one particular mutant, clone 8.14.1. These cells synthesize two forms of HLA-A2: a minor form, which remains cell-associated at all times, and an abundant form, which is secreted. The former appears by SDS-PAGE to be slightly larger than T5-1 HLA-A2, whereas the latter appears to be 4000 to 5000 daltons smaller. In vitro translation and in vivo pulse-chase studies suggest that these species are not related to each other by post-translational processing. Proteolytic digestion studies localize the resulting structural alteration in the mobility difference between wild-type and secreted HLA-A2 to a region near the carboxy terminus of the HLA-A2 heavy chain; however, their extreme carboxy termini appear similar, if not identical. We suggest that the secreted form may result from a pattern of RNA splicing in which the exon encoding the hydrophobic, membrane-spanning region is frequently deleted.
HLA - A2抗原突变体先前是通过诱变然后进行免疫选择,从B淋巴母细胞系T5 - 1中获得的。在此,我们展示了对一个特定突变体克隆8.14.1的生化研究。这些细胞合成两种形式的HLA - A2:一种是少量形式,始终与细胞相关联;另一种是大量形式,会被分泌出来。通过SDS - PAGE分析,前者似乎比T5 - 1 HLA - A2略大,而后者似乎小4000到5000道尔顿。体外翻译和体内脉冲追踪研究表明,这些物种并非通过翻译后加工相互关联。蛋白水解消化研究将野生型和分泌型HLA - A2之间迁移率差异所导致的结构改变定位到HLA - A2重链羧基末端附近的一个区域;然而,它们的极端羧基末端即使不完全相同,也似乎相似。我们认为,分泌形式可能是由一种RNA剪接模式导致的,在这种模式中,编码疏水跨膜区域的外显子经常被删除。