Evaluation of cellular dielectric spectroscopy, a whole-cell, label-free technology for drug discovery on Gi-coupled GPCRs

被引:68
作者
Peters, Matthew F.
Knappenberger, Katharine S.
Wilkins, Deidre
Sygowski, Linda A.
Lazor, Lois Ann
Liu, Jianwei
Scott, Clay W.
机构
[1] AstraZeneca Pharmaceut LP, Lead Generat Dept, Wilmington, DE 19803 USA
[2] AstraZeneca Pharmaceut LP, Dept Neurosci Biol, Wilmington, DE 19803 USA
关键词
cellular dielectric spectroscopy; GPCR; GTP gamma S binding;
D O I
10.1177/1087057106298637
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cellular dielectric spectroscopy (CDS) is an emerging technology capable of detecting a range of whole-cell responses in a label-free manner. A new CDS-based instrument, CellKey, has been developed that is optimized for G-protein coupled receptor (GPCR) detection and has automated liquid handling in microplate format, thereby making CDS accessible to lead generation/optimization drug discovery. In addition to having sufficient throughput, new assay technologies must pass rigorous standards for assay development, signal window, dynamic range, and reproducibility to effectively support drug discovery SAR studies. Here, the authors evaluated CellKey with 3 different G(i)-coupled GPCRs for suitability in supporting SAR studies. Optimized assay conditions compatible with the precision, reproducibility, and throughput required for routine screening were quickly achieved for each target. Across a 1000-fold range in compound potencies, CellKey results correlated with agonist and antagonist data obtained using classical methods ([S-35]GTP gamma S binding and cAMP production). For partial agonists, relative efficacy measurements also correlated with GTP gamma S data. CellKey detection of positive allosteric modulators appeared superior to GTP gamma S methodology. Agonist and antagonist activity could be accurately quantified under conditions of low receptor expression. CellKey is a new technology platform that uses label-free detection in a homogeneous assay that is unaffected by color quenching and is easily integrated into existing microtiter-based compound testing and data analysis procedures for drug discovery.
引用
收藏
页码:312 / 319
页数:8
相关论文
共 13 条
[1]   The novel antipsychotic aripiprazole isoforms of D2 receptors linked to is a partial agonist at short and long the regulation of adenylyl cyclase activity and prolactin release [J].
Aihara, K ;
Shimada, J ;
Miwa, T ;
Tottori, K ;
Burris, KD ;
Yocca, FD ;
Horie, M ;
Kikuchi, T .
BRAIN RESEARCH, 2004, 1003 (1-2) :9-17
[2]   Dynamic monitoring of cell adhesion and spreading on microelectronic sensor arrays [J].
Atienza, JM ;
Zhu, J ;
Wang, XB ;
Xu, X ;
Abassi, Y .
JOURNAL OF BIOMOLECULAR SCREENING, 2005, 10 (08) :795-805
[3]   Cellular dielectric spectroscopy: A powerful new approach to label-free cellular analysis [J].
Ciambrone, GJ ;
Liu, VF ;
Lin, DC ;
McGuinness, RP ;
Leung, GK ;
Pitchford, S .
JOURNAL OF BIOMOLECULAR SCREENING, 2004, 9 (06) :467-480
[4]   Monitoring of cellular behaviour by impedance measurements on interdigitated electrode structures [J].
Ehret, R ;
Baumann, W ;
Brischwein, M ;
Schwinde, A ;
Stegbauer, K ;
Wolf, B .
BIOSENSORS & BIOELECTRONICS, 1997, 12 (01) :29-41
[5]  
Gardner BR, 1997, J NEUROCHEM, V69, P2589
[6]  
LEUNG G, 2006, ASSAY DRUG DEV TECHN, V10, P258
[7]   Inverse agonism and constitutive activity as functional correlates of serotonin h5-HT1B receptor/G-protein stoichiometry [J].
Newman-Tancredi, A ;
Audinot, V ;
Moreira, C ;
Verrièle, L ;
Millan, MJ .
MOLECULAR PHARMACOLOGY, 2000, 58 (05) :1042-1049
[8]   RECEPTOR OCCUPANCY AND TISSUE RESPONSE [J].
NICKERSON, M .
NATURE, 1956, 178 (4535) :697-698
[9]   Application of real-time cell electronic sensing (RT-CES) technology to cell-based assays [J].
Solly, K ;
Wang, XB ;
Xu, X ;
Strulovici, B ;
Zheng, W .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2004, 2 (04) :363-372
[10]  
WHALEY BS, 1994, MOL PHARMACOL, V45, P481