促性腺激素释放激素受体结构和配体相互作用的研究进展。

C A Flanagan, R P Millar, N Illing
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引用次数: 48

摘要

促性腺激素释放激素(GnRH)是生殖系统的中枢调节因子,其类似物被广泛应用于多种疾病的治疗。GnRH受体是g蛋白偶联受体(gpcr)大家族的一员,具有7个跨膜结构域。对这些受体的了解有助于GnRH受体分子模型的发展,从而可以预测其三维结构以及GnRH结合和激活其受体的方式。与其他gpcr的比较发现,位于第三跨膜结构域的Lys121在激动剂结合中起作用。GnRH结构-活性研究的历史已经允许在受体的第三个细胞外环中鉴定酸性残基,这是结合哺乳动物GnRH所必需的,而合成的GnRH类似物已经表明,在第二个细胞外环中,Asn102可能与GnRH的羧基端相互作用。这些残基现在可以纳入受体模型,用于设计口服活性非肽GnRH类似物,用于避孕和治疗各种生殖疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in understanding gonadotrophin-releasing hormone receptor structure and ligand interactions.

Gonadotrophin-releasing hormone (GnRH) is the central regulator of the reproductive system and its analogues are used widely in the treatment of diverse diseases. The GnRH receptor is a member of the large family of G-protein-coupled receptors (GPCRs) which have seven transmembrane domains. Knowledge of these receptors has assisted the development of molecular models of the GnRH receptor that allow prediction of its three-dimensional configuration and the way GnRH binds and activates its receptor. Comparison with other GPCRs led to the discovery that Lys121, in the third transmembrane domain, has a role in agonist binding. The history of GnRH structure-activity studies has allowed the identification of an acidic residue in the third extracellular loop of the receptor that is required for binding of mammalian GnRH, while synthetic GnRH analogues have showed that Asn102, in the second extracellular loop, may interact with the carboxy-terminus of GnRH. These residues can now be incorporated into the receptor models that are being used to design orally active non-peptide GnRH analogues for contraception and treatment of a variety of reproductive disorders.

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