{"title":"Three HTRF methods provide sensitivity for miniaturization in high-throughput screening","authors":"Loraine V. Upham","doi":"10.1002/(SICI)1098-2728(1999)11:6<324::AID-LRA5>3.0.CO;2-E","DOIUrl":null,"url":null,"abstract":"<p>Homogeneous time-resolved fluorescence (HTRF®) assays are ideal for miniaturization in high-throughput screening. HTRF assays can be scaled down from 200 μL reactions to 25 to 70 μL reactions without loss of sensitivity. Three assay formats using proprietary europium cryptate, (Eu)K, and XL665 are described. An HTRF tyrosine kinase assay illustrates the indirect assay format. Inhibition can be detected with enzyme concentrations as low as 20 pM. An HTRF receptor-ligand binding assay is used to show a direct assay format. Reproducibility and stability are shown by a comparison of competitive binding curves under varying assay conditions. An HTRF reverse transcriptase assay is described to show the semidirect assay format. Enzyme concentrations were varied and compared with a typical [<sup>32</sup>P]-labeled assay. All three assay formats have been optimized using HTRF reagents. Results, measured in the highly sensitive Discovery® HTRF microplate analyzer, show that the sensitivity of HTRF is maintained when converting from 96-well format to 384-well format, despite the decrease in volume of reagents. © 1999 John Wiley & Sons, Inc. Lab Robotics and Automation 11: 324–329, 1999</p>","PeriodicalId":100863,"journal":{"name":"Laboratory Robotics and Automation","volume":"11 6","pages":"324-329"},"PeriodicalIF":0.0000,"publicationDate":"1999-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1098-2728(1999)11:6<324::AID-LRA5>3.0.CO;2-E","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratory Robotics and Automation","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291098-2728%281999%2911%3A6%3C324%3A%3AAID-LRA5%3E3.0.CO%3B2-E","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
Homogeneous time-resolved fluorescence (HTRF®) assays are ideal for miniaturization in high-throughput screening. HTRF assays can be scaled down from 200 μL reactions to 25 to 70 μL reactions without loss of sensitivity. Three assay formats using proprietary europium cryptate, (Eu)K, and XL665 are described. An HTRF tyrosine kinase assay illustrates the indirect assay format. Inhibition can be detected with enzyme concentrations as low as 20 pM. An HTRF receptor-ligand binding assay is used to show a direct assay format. Reproducibility and stability are shown by a comparison of competitive binding curves under varying assay conditions. An HTRF reverse transcriptase assay is described to show the semidirect assay format. Enzyme concentrations were varied and compared with a typical [32P]-labeled assay. All three assay formats have been optimized using HTRF reagents. Results, measured in the highly sensitive Discovery® HTRF microplate analyzer, show that the sensitivity of HTRF is maintained when converting from 96-well format to 384-well format, despite the decrease in volume of reagents. © 1999 John Wiley & Sons, Inc. Lab Robotics and Automation 11: 324–329, 1999
三种HTRF方法为高通量筛选的小型化提供了灵敏度
均质时间分辨荧光(HTRF®)检测是高通量筛选小型化的理想选择。HTRF检测可以从200 μL反应缩小到25 ~ 70 μL反应而不损失灵敏度。描述了使用专有的隐式铕,(Eu)K和XL665的三种分析格式。HTRF酪氨酸激酶测定说明了间接测定格式。酶的浓度低至20 pM时也能检测到抑制作用。htfr受体-配体结合试验用于显示直接的试验格式。在不同的分析条件下,竞争性结合曲线的比较显示了重现性和稳定性。描述了一种HTRF逆转录酶测定,以显示半直接测定格式。酶浓度变化,并与典型的[32P]标记法进行比较。所有三种分析格式都使用HTRF试剂进行了优化。在高灵敏度的Discovery®HTRF微孔板分析仪上测量的结果表明,尽管试剂体积减少,但从96孔格式转换为384孔格式时,HTRF的灵敏度仍保持不变。©1999 John Wiley &儿子,Inc。机械工程学报,2009,31 (2):324-329
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