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Structure-Activity Relationship Studies: Methods and Ligand Design for G-Protein Coupled Peptide Receptors

机译:结构-活性关系研究:G蛋白偶联肽受体的方法和配体设计。

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摘要

The exchange of information between cells represents an important regulatory mechanism for cellular activities. Such regulation processes mainly occur by hydrophilic compounds, unable to penetrate the cell membrane. Accordingly such signals have to be transmitted into the cell that is performed by transmembrane receptors. The widespread group of G-protein coupled receptors plays a decisive role in extracellular signal recognition and transition into cellular response. The importance of this interaction is evidently shown by the severe diseases that correlate with dysfunction of the interaction between ligand and G-protein coupled receptor. The development of drugs against these diseases needs the comprehension of signal recognition and transition as well as the understanding of intracellular signal pathways. In this review, we describe concepts and methods to identify the structure-activity relationships of G-protein coupled peptide receptors and their successful application. Furthermore we provide an insight into peptide based drug design. Examples are taken from the field of CGRP, orexin and growth hormone secretagogue receptor ligands.
机译:细胞之间的信息交换代表了细胞活动的重要调控机制。这种调节过程主要是由亲水性化合物发生的,无法穿透细胞膜。因此,必须通过跨膜受体将这种信号传输到细胞中。广泛的G蛋白偶联受体群在细胞外信号识别和转变为细胞反应中起决定性作用。与配体和G蛋白偶联受体之间的相互作用的功能障碍相关的严重疾病显然表明了这种相互作用的重要性。针对这些疾病的药物开发需要理解信号的识别和转换以及对细胞内信号通路的理解。在这篇综述中,我们描述了识别G蛋白偶联肽受体的结构活性关系及其成功应用的概念和方法。此外,我们提供了基于肽的药物设计的见解。实例取自CGRP,食欲素和生长激素促分泌素受体配体领域。

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