pubmed-article:20161830 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C0006675 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C1367690 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C0178719 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C0682972 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C0021547 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C0005971 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C1426330 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C1428424 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C1510438 | lld:lifeskim |
pubmed-article:20161830 | lifeskim:mentions | umls-concept:C1301627 | lld:lifeskim |
pubmed-article:20161830 | pubmed:dateCreated | 2010-2-17 | lld:pubmed |
pubmed-article:20161830 | pubmed:abstractText | Cell-based functional assays used for compound screening and lead optimization play an important role in drug discovery for G-protein coupled receptors (GPCRs). Cell-based assays can define the role of a compound as an agonist, antagonist or inverse agonist and can provide detailed information about the potency and efficacy of a compound. In addition, cell-based screens can be used to identify allosteric modulators that interact with sites other than the binding site of the endogenous ligand. Intracellular calcium assays which use a fluorescent calcium binding dye (such as Fluo-3, Fluo-4 or Fura-2) have been used in compound screening campaigns to measure the activity of Gq-coupled GPCRs. However, such screening methodologies require a special instrumentation to record the rapid change in intracellular free calcium concentration over time. The radioactive inositol 1,4,5- triphosphate (IP(3)) assay measures (3)H-inositol incorporation and is another traditional assay for the assessment of Gq-coupled GPCR activity, but it is not suitable for screening of large size compound collections because it requires a cell wash step and generates radioactive waste. To avoid these limitations, we have optimized and miniaturized a TR-FRET based IP-One assay that measures inositol monophosphate in a 1536-well plate format. This assay is homogenous, non-radioactive and does not require a kinetic readout. It has been tested with the cell lines expressing M(1) acetylcholine, FFAR1, vasopressin V1b, or Neuropeptide S receptors. The activities of antagonists determined in the IP-One assay correlated well with these measured in the intracellular calcium assay while the correlation of agonist activities might vary from cell line to cell line. This IP-One assay offers an alternative method for high throughput screening of Gq-coupled GPCRs without using costly kinetic plate readers. | lld:pubmed |
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pubmed-article:20161830 | pubmed:language | eng | lld:pubmed |
pubmed-article:20161830 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20161830 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
pubmed-article:20161830 | pubmed:issn | 1875-3973 | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:IngleseJamesJ | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:ZhengWeiW | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:XuKuiK | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:AustinChristo... | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:SouthallNoelN | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:TitusSteveS | lld:pubmed |
pubmed-article:20161830 | pubmed:author | pubmed-author:ZhuPingjunP | lld:pubmed |
pubmed-article:20161830 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20161830 | pubmed:volume | 1 | lld:pubmed |
pubmed-article:20161830 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20161830 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20161830 | pubmed:pagination | 70-8 | lld:pubmed |
pubmed-article:20161830 | pubmed:dateRevised | 2010-9-28 | lld:pubmed |
pubmed-article:20161830 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:20161830 | pubmed:articleTitle | Comparison on functional assays for Gq-coupled GPCRs by measuring inositol monophospate-1 and intracellular calcium in 1536-well plate format. | lld:pubmed |
pubmed-article:20161830 | pubmed:affiliation | NIH Chemical Genomics Center, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-3370, USA. | lld:pubmed |
pubmed-article:20161830 | pubmed:publicationType | Journal Article | lld:pubmed |