Cullen S E, David C S, Shreffler D C, Nathenson S G
Proc Natl Acad Sci U S A. 1974 Mar;71(3):648-52. doi: 10.1073/pnas.71.3.648.
Membrane associated molecules that are probably glycoproteins could be specifically precipitated from NP-40 detergent solubilized extracts of radiolabeled mouse spleen or lymph node cells by antisera produced in congenic strain combinations differing only in the Ir gene region which is linked to the H-2 genes. These Ir region products were designated Lna (lymph node antigen) to conform to previous serological work.Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of unreduced specific immune precipitates revealed the presence of a possible dimer form, while reduced samples showed only a single peak equivalent to 30,000 daltons. Thus the Lna molecules are clearly distinct from the H-2D and H-2K molecules, which are about 45,000 daltons. Anti-Lna antibodies of different specificity can be present in a single serum; there were at least two separate antigen molecules present in one haplotype tested.
可能是糖蛋白的膜相关分子,可从经放射性标记的小鼠脾脏或淋巴结细胞的NP - 40去污剂溶解提取物中,被仅在与H - 2基因连锁的Ir基因区域不同的同基因品系组合中产生的抗血清特异性沉淀。这些Ir区域产物被命名为Lna(淋巴结抗原),以符合先前的血清学研究。未还原的特异性免疫沉淀物的十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳显示存在一种可能的二聚体形式,而还原后的样品仅显示一个相当于30,000道尔顿的单峰。因此,Lna分子明显不同于约45,000道尔顿的H - 2D和H - 2K分子。不同特异性的抗Lna抗体可存在于单一血清中;在所测试的一个单倍型中至少存在两个独立的抗原分子。