Schwartz B D, Kask A M, Paul W E, Shevach E M
J Exp Med. 1976 Mar 1;143(3):541-58. doi: 10.1084/jem.143.3.541.
The GPLA B and Ia (I region-associated) antigens are the products of genes found in the guinea pig major histocompatibility complex. Because of their importance in immune response phenomena, a structural study of these antigens was undertaken. [3H]leucine and [3H]fucose were internally incorporated into guinea pig lymph node cells. The GPLA B and Ia antigens were solubilized by the nonionic detergent Nonidet P-40, purified by affinity chromatography using an adsorbent column of lentil lectin, isolated by immunoprecipitation, and examined by discontinuous polyacrylamide-sodium dodecyl sulfate gel electrophoresis. The GPLA antigens B.1, B.2, B.3, and B.4, were shown to be glycoproteins of mol wt 40,000 daltons and to be noncovalently associated with a 12,000 dalton protein. The molecules bearing B.2 and B.3 in a B.2/B.3 heterozygote are shown to be separable, suggesting the antigenic determinant is a primary gene product. In addition, a new GPLA determinant, S, which resembles the B antigen in that it is found on a molecule of approximately 40,000 daltons, was studied. In a B.2/B.3 S+ animal the molecule bearing antigen S was shown to be independent of those bearing B.2 and B.3, providing evidence that the genes determining B and S are at separate loci. The Ia-bearing molecules identified by anti-Ia.2,4 are glycoproteins of mol wt 58,000 daltons which are composed of two subunits of 33,000 and 25,000 daltons, respectively, linked by disulfide bonds. The Ia-bearing molecules are independent of GPLA-bearing molecules, indicating different loci determining these antigens. By all criteria, the guinea pig GPLA B antigens appear homologous to the murine H-2D and H-2K antigens, while the guinea pig Ia antigens appear homologous to the Ia antigens of the mouse.
豚鼠GPLA B抗原和Ia(I区相关)抗原是豚鼠主要组织相容性复合体中基因的产物。由于它们在免疫反应现象中的重要性,对这些抗原进行了结构研究。用[³H]亮氨酸和[³H]岩藻糖对豚鼠淋巴结细胞进行内源性掺入。用非离子去污剂Nonidet P - 40使GPLA B抗原和Ia抗原溶解,通过使用扁豆凝集素吸附柱的亲和层析进行纯化,通过免疫沉淀进行分离,并通过不连续聚丙烯酰胺 - 十二烷基硫酸钠凝胶电泳进行检测。结果显示,GPLA抗原B.1、B.2、B.3和B.4是分子量为40,000道尔顿的糖蛋白,并且与一种12,000道尔顿的蛋白质非共价结合。在B.2/B.3杂合子中携带B.2和B.3的分子被证明是可分离的,这表明抗原决定簇是一个初级基因产物。此外,还研究了一种新的GPLA决定簇S,它与B抗原相似,存在于大约40,000道尔顿的分子上。在B.2/B.3 S⁺动物中,携带抗原S的分子被证明独立于携带B.2和B.3的分子,这为决定B和S的基因位于不同位点提供了证据。用抗Ia.2,4鉴定的携带Ia的分子是分子量为58,000道尔顿的糖蛋白,由分别为33,000道尔顿和25,000道尔顿的两个亚基通过二硫键连接而成。携带Ia的分子独立于携带GPLA的分子,表明决定这些抗原的基因位点不同。从各方面标准来看,豚鼠GPLA B抗原似乎与小鼠的H - 2D和H - 2K抗原同源,而豚鼠Ia抗原似乎与小鼠的Ia抗原同源。