Lee Y J, Strott C A
Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, Bethesda, Maryland 20892.
Biochem Biophys Res Commun. 1988 Jan 15;150(1):456-62. doi: 10.1016/0006-291x(88)90542-6.
Pregnenolone-binding activity isolated from the cytosol of the guinea pig adrenal cortex appears to correspond to a Mr 34,000 protein when examined by SDS-polyacrylamide gel electrophoresis during different stages of purification. To verify this finding the Mr 34,000 protein band was eluted from the SDS gel and used to generate a polyclonal antibody. Immobilized anti 34,000 IgG on protein A-Sepharose was found to extract pregnenolone-binding activity from solution in contrast to pre-immune IgG and an antibody raised against a Mr 30,000 protein isolated simultaneously. In addition, protein eluted from the protein A-anti 34,000 IgG complex exhibited the expected molecular weight of 34,000 when examined on an SDS gel. These results, thus, confirm that the pregnenolone-binding protein is indeed a protein of Mr 34,000.
从豚鼠肾上腺皮质胞质溶胶中分离出的孕烯醇酮结合活性,在纯化的不同阶段通过SDS-聚丙烯酰胺凝胶电泳检测时,似乎对应于一种分子量为34,000的蛋白质。为了验证这一发现,从SDS凝胶上洗脱分子量为34,000的蛋白质条带,并用于制备多克隆抗体。与免疫前IgG和同时分离出的针对一种分子量为30,000蛋白质产生的抗体相比,发现固定在蛋白A-琼脂糖上的抗34,000 IgG能从溶液中提取孕烯醇酮结合活性。此外,从蛋白A-抗34,000 IgG复合物上洗脱的蛋白质在SDS凝胶上检测时,显示出预期的分子量34,000。因此,这些结果证实孕烯醇酮结合蛋白确实是一种分子量为34,000的蛋白质。