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催乳素受体:通过亲和标记鉴定结合单位以及多克隆和单克隆抗体的特性研究

Prolactin receptor: identification of the binding unit by affinity labelling and characterization of poly- and monoclonal antibodies.

作者信息

Djiane J, Kelly P A, Katoh M, Dusanter-Fourt I

出版信息

Horm Res. 1985;22(3):179-88. doi: 10.1159/000180092.

Abstract

The prolactin receptor localized in rabbit mammary gland membranes has been identified by affinity labelling using covalent cross-linking agents such as a unique protein chain of approximately 32,000 daltons. After partial purification (5,000-fold) of these receptors from mammary gland homogenate, polyclonal antibodies, which specifically and completely inhibit prolactin binding in all organs and in all species studied, were raised. These antibodies possessed prolactin-like biological activity (casein synthesis) on rabbit mammary gland explants. Monoclonal antibodies specifically directed against the binding domain of the receptor were also obtained. These antibodies were more species-specific than the polyclonal antibodies. The most potent (M110) possessed higher affinity than prolactin for the receptor and could be a very effective tool to elucidate the structure of the receptor and its immunological detection.

摘要

利用诸如独特的约32,000道尔顿蛋白质链的共价交联剂进行亲和标记,已鉴定出兔乳腺膜中的催乳素受体。从乳腺匀浆中对这些受体进行部分纯化(5000倍)后,制备了多克隆抗体,该抗体能特异性且完全抑制所研究的所有器官和所有物种中的催乳素结合。这些抗体对兔乳腺外植体具有催乳素样生物活性(酪蛋白合成)。还获得了特异性针对受体结合域的单克隆抗体。这些抗体比多克隆抗体具有更强的物种特异性。最有效的(M110)对受体的亲和力高于催乳素,可能是阐明受体结构及其免疫检测的非常有效的工具。

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