Palfree R G, Dumont F J, Hammerling U
Immunogenetics. 1986;23(3):197-207. doi: 10.1007/BF00373821.
Rat monoclonal antibodies YE3/19.1, defining the murine-activated lymphocyte antigen MALA-1, and D7, detecting an Ly-6 locus-controlled antigen, bound highly purified Ly-6E.1. On western blots of lymphocyte surface proteins which had been solubilized and electrophoretically separated in octylglucoside, they detected bands which comigrated with Ly-6A.2 or Ly-6E.1 antigens. On cells or in an immunoassay they blocked alloantibodies against Ly-6A.2 or Ly-6E.1. The tissue distribution of MALA-1 also correlated with Ly-6A.2 or Ly-6E.1. Upon octylglucoside or sodium dodecyl sulfate-polyacrylamide gel electrophoresis, these antigens displayed similar sizes. Thus, Ly-6A.2 and Ly-6E.1 are most likely products of alternate alleles. Electrophoretic analysis showed a similar size and charge for Ly-6A.2, Ly-6B.2, Ly-6D.2, and Ly-27.2. Ly-6C.2 and Ly-28.2 appeared to be identical, and were similar in size to Ly-6A.2, but they differed in charge and in intrachain disulfide constraints. Since Ly-6D.2 and Ly-27.2 may represent the same or different epitopes on the Ly-6A.2 molecule, the previously postulated five Ly-6-like antigens that were thought to be separable on the basis of tissue distribution, may represent no more than three separate proteins which can be assigned to one of two distinct categories by electrophoretic mobility in gels containing octylglucoside.
识别小鼠活化淋巴细胞抗原MALA-1的大鼠单克隆抗体YE3/19.1和检测Ly-6位点控制抗原的D7与高度纯化的Ly-6E.1结合。在经辛基葡萄糖苷溶解并进行电泳分离的淋巴细胞表面蛋白的western印迹中,它们检测到与Ly-6A.2或Ly-6E.1抗原迁移率相同的条带。在细胞上或免疫测定中,它们可阻断针对Ly-6A.2或Ly-6E.1的同种抗体。MALA-1的组织分布也与Ly-6A.2或Ly-6E.1相关。经辛基葡萄糖苷或十二烷基硫酸钠-聚丙烯酰胺凝胶电泳后,这些抗原显示出相似的大小因此,Ly-6A.2和Ly-6E.1很可能是等位基因变体的产物。电泳分析表明,Ly-6A.2、Ly-6B.2、Ly-6D.2和Ly-27.2具有相似的大小和电荷。Ly-6C.2和Ly-28.2似乎是相同的,并且大小与Ly-6A.2相似,但它们在电荷和链内二硫键限制方面有所不同。由于Ly-6D.2和Ly-27.2可能代表Ly-6A.2分子上相同或不同的表位,因此先前假定的五种基于组织分布可分离的Ly-6样抗原,可能代表不超过三种不同的蛋白质,根据在含有辛基葡萄糖苷的凝胶中的电泳迁移率,可将它们分为两个不同类别中的一类。