Ymer S I, Herington A C
Biochem J. 1987 Mar 15;242(3):713-20. doi: 10.1042/bj2420713.
Covalent cross-linking techniques have been used to investigate the structural characteristics of the growth-hormone (GH) receptor in a variety of rabbit liver cell membrane preparations (particulate and soluble). Two classes of GH-binding protein have been identified which differ in their Mr by gel filtration and susceptibility to precipitation with poly(ethylene glycol) (PEG). The first, a PEG-precipitable (Mr approximately 300,000) protein, contained Mr-65,000 and Mr-40,000 binding proteins linked by disulphide bonds. It was present in aqueous extracts derived from microsomal membranes but was not present in cytosol preparations. The second, a PEG-non-precipitable protein (Mr approximately 100,000) was composed of a non-disulphide-linked primary GH-binding subunit of Mr 60,000-66,000. This binding protein was present in all rabbit liver cell fractions and/or preparations. Both binding-protein classes contained intramolecular disulphide bonds. It is not clear whether the Mr-approximately 100,000 form, or perhaps higher-Mr species which have not been identified by cross-linking studies, represents the native, endogenous, form of the GH receptor present in particulate microsomal or plasma membranes. Accordingly, although these data have identified two classes of GH-binding protein, especially a primary GH-binding subunit of Mr 60,000-66,000, they indicate that, unlike studies on the insulin receptor, covalent cross-linking techniques alone are not sufficient to delineate the complete subunit structure of the native and endogenous form of the GH receptor.
共价交联技术已被用于研究多种兔肝细胞膜制剂(微粒体和可溶性)中生长激素(GH)受体的结构特征。已鉴定出两类GH结合蛋白,它们通过凝胶过滤法测定的相对分子质量(Mr)以及对聚乙二醇(PEG)沉淀的敏感性不同。第一类是一种可被PEG沉淀的蛋白(Mr约为300,000),它包含通过二硫键相连的Mr为65,000和Mr为40,000的结合蛋白。它存在于微粒体膜的水提取物中,但不存在于胞质溶胶制剂中。第二类是一种不可被PEG沉淀的蛋白(Mr约为100,000),由一个Mr为60,000 - 66,000的非二硫键连接的主要GH结合亚基组成。这种结合蛋白存在于所有兔肝细胞组分和/或制剂中。两类结合蛋白都含有分子内二硫键。目前尚不清楚Mr约为100,000的形式,或者可能是尚未通过交联研究鉴定出的更高Mr的物种,是否代表存在于微粒体或质膜中的天然、内源性GH受体形式。因此,尽管这些数据已鉴定出两类GH结合蛋白,特别是一个Mr为60,000 - 66,000的主要GH结合亚基,但它们表明,与胰岛素受体的研究不同,仅靠共价交联技术不足以描绘出天然和内源性GH受体的完整亚基结构。