Dobberstein B, Kvist S, Roberts L
Philos Trans R Soc Lond B Biol Sci. 1982 Dec 24;300(1099):161-72. doi: 10.1098/rstb.1982.0163.
Histocompatibility antigens (H-2K, D and L, and HLA-A, B and C) are highly polymorphic cell surface proteins. Their primary structure has been determined by sequencing the protein, complementary DNAs (cDNAs) or genes in several laboratories. H-2Ld and Kd antigens are encoded by eight separate exons: one encodes the signal sequence, three encode the external domains, one encodes the membrane spanning segment and three encode the cytoplasmic domain. A similar structural organization has been found for an HLA gene. H-2 and HLA antigens are synthesized on membrane-bound ribosomes and are co-translationally inserted into the membrane of the endoplasmic reticulum. Here they assemble with beta 2-microglobulin, a small secretory protein. We describe the structure, the membrane insertion in vitro and in vivo, the intracellular transport and the surface expression of these antigens.
组织相容性抗原(H-2K、D和L,以及HLA-A、B和C)是高度多态性的细胞表面蛋白。它们的一级结构已通过多个实验室对蛋白质、互补DNA(cDNA)或基因进行测序而确定。H-2Ld和Kd抗原由八个独立的外显子编码:一个编码信号序列,三个编码外部结构域,一个编码跨膜区段,三个编码胞质结构域。已发现HLA基因具有类似的结构组织。H-2和HLA抗原在膜结合核糖体上合成,并在翻译过程中共同插入内质网的膜中。在这里,它们与一种小分泌蛋白β2-微球蛋白组装在一起。我们描述了这些抗原的结构、在体外和体内的膜插入、细胞内运输以及表面表达。