Validation of FLIPR Membrane Potential Dye for High Throughput Screening of Potassium Channel Modulators

A fluorescence-based assay using the FLIPR Membrane Potential Assay Kit (FMP) was evaluated for functional characterization and high throughput screening (HTS) of potassium channel (ATP-sensitive Ki channel; KATP) modulators. The FMP dye permits a more sensitive evaluation of changes in membrane potential with a more rapid response time relative to DiBAC4(3). The time course of responses is comparable to ligand-evoked activation of the channel measured by patch-clamp studies. The pharmacological profile of the K+ channel evaluated by using reference KATP channel openers is in good agreement with that derived previously by DiBAC4(3)-based FLIPR assays. Improved sensitivity of responses together with the diminished susceptibility to artifacts such as those evoked by fluorescent compounds or quenching agents makes the FMP dye an alternative choice for HTS screening of potassium channel modulators.

[1]  Brian Cox,et al.  HTS approaches to voltage-gated ion channel drug discovery , 1998 .

[2]  J. Sullivan,et al.  Characterization of the ATP-sensitive potassium channels (KATP) expressed in guinea pig bladder smooth muscle cells. , 1999, The Journal of pharmacology and experimental therapeutics.

[3]  L. Mattheakis,et al.  Assay technologies for screening ion channel targets. , 2001, Current opinion in drug discovery & development.

[4]  D. Epps,et al.  Characterization of the steady-state and dynamic fluorescence properties of the potential-sensitive dye bis-(1,3-dibutylbarbituric acid)trimethine oxonol (Dibac4(3)) in model systems and cells. , 1994, Chemistry and physics of lipids.

[5]  England Discovering ion-channel modulators - making the electrophysiologist's life more interesting. , 1999, Drug discovery today.

[6]  S. Enna Current protocols in pharmacology , 1998 .

[7]  J. Sullivan,et al.  Pharmacological and molecular analysis of ATP-sensitive K(+) channels in the pig and human detrusor. , 2000, European journal of pharmacology.

[8]  A. Bonev,et al.  ATP-sensitive potassium channels in smooth muscle cells from guinea pig urinary bladder. , 1993, The American journal of physiology.

[9]  P. Negulescu,et al.  Cell-based assays and instrumentation for screening ion-channel targets. , 1999, Drug discovery today.

[10]  J. Sullivan,et al.  Functional implication of spare ATP-sensitive K(+) channels in bladder smooth muscle cells. , 2001, The Journal of pharmacology and experimental therapeutics.