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Fluorescence-Based Tl+−Influx Assays as a Novel Approach for Characterization of Small-Conductance Ca2+−Activated K+ Channel Modulators

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Potassium Channels

Part of the book series: Methods in Molecular Biology ((MIMB,volume 491))

Summary

Small-conductance Ca2+−activated potassium (SK) channels constitute a family of ion channels that are regulated by the cytosolic Ca2+ concentration. Increases in the intracellular Ca2+ concentration ([Ca2+]i) result in opening of the channels, which in turn will lead to changes in the membrane potential. As the name implies, the channels are of small conductance, but even so, they are known to play a crucial role in several physiological processes, such as modulation of neurotransmitter and hormone secretion, as well as memory and learning (e.g.,see Curr Med Chem 14:1437–1457, 2007). Owing to the central role of SK channels, they have attracted much attention as potential drug targets, both with respect to identification of activators and blockers of SK channel activity for indications such as, e.g., epilepsy, pain, and urinary incontinence (see Curr Med Chem 14:1437–1457, 2007; Curr Pharm Des 12:397–406, 2006). Thus, great efforts have been put into the development of robust high-throughput assays for detection and characterization of modulators of SK channel activity. In the present chapter, we describe two fluorescence-based Tl+influx assays for detection of positive and negative SK channel modulators.

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References

  1. Wulff, H., Kolski-Andr eaco, A., Sankaranarayanan, A., Sabatier, J.-M., and Shakkottai V (2007) Modulators of small- and intermediate-conductance calcium-activated potassium channels and their therapeutic indications. Current Medicinal Chemistry 14, 1437–1457.

    Article  CAS  PubMed  Google Scholar 

  2. Trehene, J.M. (2006) Exploiting high-throughput ion channel screening technologies in integrated drug discovery. Current Pharmaceutical Design 12, 397–406.

    Article  Google Scholar 

  3. Gonzβlez, J.E. and Maher, M.P. (2002) Cellular fluorescent indicators and voltage/ion probe reader (VIPR™): tools for ion channel and receptor drug discovery. Receptors & Channels 8, 283–295.

    Article  Google Scholar 

  4. Weaver, C.D., Harden, D., Dworetzky, S.I., Robertson, B., and Knox, R.J. (2004) A thallium-sensitive, fluorescence-based assay for detecting potassium channel modulators in mammalian cells. Journal of Biomolecular Screening 9, 671–677.

    Article  CAS  PubMed  Google Scholar 

  5. Strϕbæk, D., Teuber, L., Jϕrgensen, T.D., Ahring, P.K., Kjær, K., Hansen, R.S., Olesen, S.P., Christophersen, P., and Skaaning-Jensen, B. (2004) Activation of human IK and SK Ca2+− activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime). Biochimica et Biophysica Acta 1665, 1–5.

    Google Scholar 

  6. Hougaard, C., Eriksen, B.L., Jϕrgensen, S., Johansen, T.H., Dyhring, T., Madsen, L.S., Strϕbæk, D., and Christophersen, P. (2007) British Journal of Pharmacology 151, 655–665.

    Article  CAS  PubMed  Google Scholar 

  7. Strϕbæk, D., Hougaard, C., Johansen, T.H., Sϕrensen, U.S., Nielsen, E.∅., Nielsen, K.S., Taylor, R.D.T., Pedarzani, P., and Christo-phersen, P. (2006) Inhibitory gating modulation of small conductance Ca2+−activated K+ channels by the synthetic compound (R)-N-(Benzimidazol-2-yl)-1,2,3,4-tet-rahydro-1-naphtylamine (NS8593) reduces afterhyperpolarizing current in hippocampal CA1 neurons. Molecular Pharmacology 70, 1771–1782.

    Article  Google Scholar 

  8. Moore, H.-P.H. and Raftery, M.A. (1980) Direct spectroscopic studies of cation translo-cation by Torpedo acetylcholine receptor on a time scale of physiological relevance. Proceedings of the National Academy of Sciences of the United States of America 77, 4509–4513.

    Article  CAS  PubMed  Google Scholar 

  9. Ishii, T.M., Silvia, C., Hirschberg, B., Bond, C.T., Adelman, J.P., and Maylie, J. (1997) A human intermediate conductance calcium-activated potassium channel. Proceedings of the National Academy of Sciences of the United States of America 94, 11651–11656.

    Article  CAS  PubMed  Google Scholar 

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Jϕrgensen, S., Johansen, T.H., Dyhring, T. (2008). Fluorescence-Based Tl+−Influx Assays as a Novel Approach for Characterization of Small-Conductance Ca2+−Activated K+ Channel Modulators. In: Lippiat, J.D. (eds) Potassium Channels. Methods in Molecular Biology, vol 491. Humana Press. https://doi.org/10.1007/978-1-59745-526-8_20

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  • DOI: https://doi.org/10.1007/978-1-59745-526-8_20

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-934115-65-7

  • Online ISBN: 978-1-59745-526-8

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