Massague J, Guillette B J, Czech M P
J Biol Chem. 1981 Mar 10;256(5):2122-5.
Plasma membranes from rat adipocytes and liver and from human placenta have been labeled by covalent cross-linking to membrane-bound 125I-labeled multiplication stimulating activity (125I-MSA) with three different bishydroxysuccinimide esters: disuccinimidyl suberate, disuccinimidyl succinate, and ethyleneglycolyl bis(succinimidyl succinate). Dodecyl sulfate-polyacrylamide gel electrophoresis and autoradiographic analysis of the 125I-MSA-labeled material in the presence of dithiothreitol reveals one single-labeled protein migrating with an apparent Mr = 255,000 regardless of the kind and concentration of cross-linker used. Electrophoresis in the absence of reductant indicates that the affinity-labeled species is not disulfide-linked to any other protein in the native plasma membrane, but contains internal disulfide bonds that compact its structure. The labeling of the Mr = 255,000 species increases with increasing concentrations of 125I-MSA between 0.3 and 3 nM. Labeling is abolished in a competitive manner by nonradioactive MSA but not by similar concentrations of insulin, proinsulin, or epidermal growth factor in all three tissues examined. The unique labeling of this Mr = 225,000 membrane component and its selective inhibition by MSA suggest that this protein is a plasma membrane receptor for MSA.
大鼠脂肪细胞、肝脏以及人胎盘的质膜已通过与膜结合的125I标记的增殖刺激活性(125I-MSA)进行共价交联而被标记,所用的三种不同双羟基琥珀酰亚胺酯分别为:辛二酸二琥珀酰亚胺酯、琥珀酸二琥珀酰亚胺酯以及乙二醇双(琥珀酰亚胺琥珀酸酯)。在二硫苏糖醇存在的情况下,对125I-MSA标记的物质进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和放射自显影分析,结果显示无论使用何种交联剂及其浓度如何,均有一条单一标记的蛋白质迁移,其表观分子量Mr = 255,000。在没有还原剂的情况下进行电泳表明,亲和标记的物质在天然质膜中并非通过二硫键与任何其他蛋白质相连,而是含有内部二硫键,这些二硫键使其结构紧密。Mr = 255,000物质的标记随着0.3至3 nM之间125I-MSA浓度的增加而增加。在所检测的所有三种组织中,非放射性MSA以竞争方式消除标记,但相同浓度的胰岛素、胰岛素原或表皮生长因子则不会。这种Mr = 225,000膜成分的独特标记及其被MSA的选择性抑制表明,该蛋白质是MSA的质膜受体。