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G蛋白偶联受体药物研发的最新进展。

Latest development in drug discovery on G protein-coupled receptors.

作者信息

Lundstrom Kenneth

机构信息

BioXtal,Chemin des Croisettes 22, CH-1066 Epalinges, Switzerland.

出版信息

Curr Protein Pept Sci. 2006 Oct;7(5):465-70. doi: 10.2174/138920306778559403.

Abstract

G protein-coupled receptors (GPCRs) represent the family of proteins with the highest impact from social, therapeutic and economic point of view. Today, more than 50% of drug targets are based on GPCRs and the annual worldwide sales exceeds 50 billion dollars. GPCRs are involved in all major disease areas such as cardiovascular, metabolic, neurodegenerative, psychiatric, cancer and infectious diseases. The classical drug discovery process has relied on screening compounds, which interact favorably with the GPCR of interest followed by further chemical engineering as a mean of improving efficacy and selectivity. In this review, methods for sophisticated chemical library screening procedures will be presented. Furthermore, development of cell-based assays for functional coupling of GPCRs to G proteins will be discussed. Finally, the possibility of applying structure-based drug design will be summarized. This includes the application of bioinformatics knowledge and molecular modeling approaches in drug development programs. The major efforts established through large networks of structural genomics on GPCRs, where recombinantly expressed GPCRs are subjected to purification and crystallization attempts with the intention of obtaining high-resolution structures, are presented as a promising future approach for tailor-made drug development.

摘要

从社会、治疗和经济角度来看,G蛋白偶联受体(GPCRs)是影响最大的一类蛋白质。如今,超过50%的药物靶点基于GPCRs,全球年销售额超过500亿美元。GPCRs涉及所有主要疾病领域,如心血管疾病、代谢性疾病、神经退行性疾病、精神疾病、癌症和传染病。传统的药物发现过程依赖于筛选与目标GPCR有良好相互作用的化合物,随后进行进一步的化学工程改造以提高疗效和选择性。在本综述中,将介绍复杂化学文库筛选程序的方法。此外,还将讨论用于GPCRs与G蛋白功能偶联的基于细胞的检测方法的开发。最后,将总结应用基于结构的药物设计的可能性。这包括在药物开发项目中应用生物信息学知识和分子建模方法。通过大型GPCRs结构基因组学网络所做的主要工作也将被介绍,在这些工作中,重组表达的GPCRs经过纯化和结晶尝试,旨在获得高分辨率结构,这是定制药物开发的一种有前景的未来方法。

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