Conn P Michael, Smith Emery, Spicer Timothy, Chase Peter, Scampavia Louis, Janovick Jo Ann
1 Departments of Internal Medicine and Cell Biology/Biochemistry, Texas Tech University Health Sciences Center , Lubbock, Texas.
Assay Drug Dev Technol. 2014 May;12(4):238-46. doi: 10.1089/adt.2014.576.
We describe a phenotypic high throughput screening (HTS) calcium flux assay designed to identify pharmacoperones for the gonadotropin releasing hormone receptor (GnRHR). Pharmacoperones are target-specific, small molecules that diffuse into cells, rescue misfolded protein mutants, and restore them to function. Rescue is based on correcting the trafficking of mutants that would otherwise be retained in the endoplasmic reticulum and unable to function correctly. This approach identifies drugs with a significant degree of novelty, relying on cellular mechanisms that are not currently exploited. Development of such assays is important, since the extensive use of agonist/antagonist screens alone means that useful chemical structures may be present in existing libraries but have not been previously identified using existing methods. Our assay utilizes cell lines stably expressing a GnRHR mutant under the control of a tetracycline (OFF) transactivator. This allows us to quantitate the level of functional and properly trafficked G protein coupled receptors present in each test well. Furthermore, since we are able to turn receptor expression on and off, we can rapidly eliminate the majority of false positives from our screening results. Our data show that this approach is likely to be successful in identifying hits from large chemical libraries.
我们描述了一种表型高通量筛选(HTS)钙流测定法,旨在鉴定促性腺激素释放激素受体(GnRHR)的药效伴侣。药效伴侣是靶向特异性小分子,可扩散进入细胞,拯救错误折叠的蛋白质突变体并使其恢复功能。拯救是基于纠正那些否则会滞留在内质网中且无法正常发挥功能的突变体的转运。这种方法依赖于目前未被利用的细胞机制来鉴定具有高度新颖性的药物。开发此类测定法很重要,因为仅广泛使用激动剂/拮抗剂筛选意味着现有文库中可能存在有用的化学结构,但以前使用现有方法尚未鉴定出来。我们的测定法利用在四环素(关闭)反式激活因子控制下稳定表达GnRHR突变体的细胞系。这使我们能够定量每个测试孔中存在的功能性且正确转运的G蛋白偶联受体的水平。此外,由于我们能够开启和关闭受体表达,我们可以迅速从筛选结果中消除大多数假阳性。我们的数据表明,这种方法很可能成功地从大型化学文库中鉴定出命中物。