Colette Jean, Avé Emilie, Grenier-Boley Benjamin, Coquel Anne-Sophie, Lesellier Karine, Puget Karine
Genepep S.A., Zone d'activité les Baronnes, Ateliers Relais, Lots 4 & 5, 34 730 Prades le Lez, France.
J Pept Sci. 2007 Sep;13(9):568-74. doi: 10.1002/psc.898.
Owing to their involvement in many physiological and pathological processes, G-protein-coupled receptors (GPCRs) are interesting targets for drug development. Approximately, 100 endoGPCRs lack their natural ligands and remain orphan (oGPCRs). Consequently, oGPCR deorphanization appears a promising research field for the development of new therapeutics. On the basis of the knowledge of currently known GPCR/ligand couples, some oGPCRs may be targeted by peptides. However, to find new drugs for GPCRs, Genepep has developed a dedicated bioinformatics platform to screen transcriptomic databases for the prediction of new GPCR ligands. The peptide lists generated include specific data, such as chemical and physical properties, the occurrence of post-translational modifications (PTMs) and an annotation referring to the location and expression level of the related putative genes. This information system allows a selection through series of biological criteria of approximately 10 000 natural peptides including already known GPCR ligands and potential new candidates for GPCR deorphanization. The most promising peptides for functional assay screening and future development as therapeutic agents are under evaluation.
由于参与许多生理和病理过程,G蛋白偶联受体(GPCRs)是药物开发中令人感兴趣的靶点。大约有100种内源性GPCRs缺乏天然配体,仍然是孤儿受体(oGPCRs)。因此,oGPCRs的去孤儿化似乎是开发新疗法的一个有前景的研究领域。基于目前已知的GPCR/配体对的知识,一些oGPCRs可能被肽靶向。然而,为了找到针对GPCRs的新药,Genepep开发了一个专门的生物信息学平台,用于筛选转录组数据库以预测新的GPCR配体。生成的肽列表包括特定数据,如化学和物理性质、翻译后修饰(PTMs)的出现情况以及与相关假定基因的位置和表达水平相关的注释。这个信息系统允许通过一系列生物学标准从大约10000种天然肽中进行筛选,这些肽包括已知的GPCR配体和oGPCRs去孤儿化的潜在新候选物。最有希望用于功能测定筛选和未来作为治疗药物开发的肽正在评估中。