Rubidium Efflux Assay for the Determination of Calcium Activated Potassium Channel Activity

  • Zainab Gambo Ibrahim Department of Clinical Pharmacology and Therapeutics, Faculty of Basic Clinical Sciences, College of Medical Sciences, Abubakar Tafawa Balewa University, Bauchi, Nigeria
  • Hussein A Saad Elrewey Institute of Cancer Therapeutics, University of Bradford, United Kingdom, And Faculty of pharmacy, University of Benghazi, State of Libya
Keywords: Rubidium efflux, Flame atomic absorption spectrometry, BKα channel, HEK293 cells, NS1619, 50mM and 80mM KBS.


Rubidium efflux assay using flame atomic absorption spectrometry is employed in analyzing potassium channel activity. Calibration using standards of known R  concentrations (10 - 100µM) in tubes was done at the beginning and end of each analysis. R  standard curves were constructed from the data obtained from the analysis of the R standards in both the tubes and 96 well plates. HEK293 cells expressing the alpha subunit of BK channel were incubated with R  for 4 hours after which the cells were washed and then treated with higher concentrations of KBS (50mM / 80mM) or NS1619 (0.003 - 100µM) for 10 minutes. The supernatant was removed and the cells lysed with 0.1%v/v triton. The percentage efflux was then determined from values obtained after analyzing the supernatant and lysate using flame atomic absorption spectrometer. The results showed that there was consistency during each analysis as the R  standard curves constructed from the data obtained overlapped with no significant difference indicating precise calibration and internal validation. For the loaded cells (un-treated), the average concentration of R    in the supernatant was 14.47µM while that in the lysate was 56.24µM and statistical analysis showed there was a significant difference with p<0.0001. The treated cells with higher concentrations of KBS in comparison with 5.4mM KBS gave a percentage increase in R efflux of 47.8% for50mM KBS with significant different of p<0.0001 and 80.11% increase with significant different of p<0.05 for 80mM KBS. The treated cells with 0.1, 0.01 and 0.003µM NS1619 gave a percentage increase in efflux of 13.98%, 29.95% and 23.69% respectively. This research indicated the viability of using flame atomic absorption spectrometry for rubidium efflux assay to test for compounds activating effect on BK channel.


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Bentzen, B. H., Olesen, S. P., Rønn, L. C., & Grunnet, M. (2014). BK channel activators and their therapeutic perspectives. Frontiers in physiology, 5, 389.

Ge, L., Hoa, N. T., Wilson, Z., Arismendi-Morillo, G., Kong, X. T., Tajhya, R. B., ... & Jadus, M. R. (2014). Big Potassium (BK) ion channels in biology, disease and possible targets for cancer immunotherapy. International immunopharmacology, 22(2), 427-443.

Ghatta, S., Nimmagadda, D., Xu, X., & O'Rourke, S. T. (2006). Large-conductance, calcium-activated potassium channels: structural and functional implications. Pharmacology & therapeutics, 110(1), 103-116.

Ibrahim, Z. G. (2015) Rubidium efflux assay using flame atomic absorption spectrometry as a measure for BK channel activity. [Master’s thesis]. [Sheffield (UK)]: Sheffield Hallam University

Kirby, R. W., Martelli, A., Calderone, V., McKay, N. G., & Lawson, K. (2013). Large conductance Ca2+-activated K+ channel (BKCa) activating properties of a series of novel N-arylbenzamides: Channel subunit dependent effects. Bioorganic & medicinal chemistry, 21(14), 4186-4191.

McKay, N. G., Kirby, R. W., & Lawson, K. (2008). Rubidium efflux as a tool for the pharmacological characterisation of compounds with BK channel opening properties. In Potassium Channels (pp. 267-277). Humana Press.

Olesen, S. P., Munch, E., Moldt, P., & Drejer, J. (1994). Selective activation of Ca2+-dependent K+ channels by novel benzimidazolone. European journal of pharmacology, 251(1), 53-59.

Scott, C. W., Wilkins, D. E., Trivedi, S., & Crankshaw, D. J. (2003). A medium-throughput functional assay of KCNQ2 potassium channels using rubidium efflux and atomic absorption spectrometry. Analytical biochemistry, 319(2), 251-257.

Szewczyk, A., Kajma, A., Malinska, D., Wrzosek, A., Bednarczyk, P., Zabłocka, B., & Dołowy, K. (2010). Pharmacology of mitochondrial potassium channels: dark side of the field. FEBS letters, 584(10), 2063-2069.

Terstappen, G. C. (1999). Functional analysis of native and recombinant ion channels using a high-capacity nonradioactive rubidium efflux assay. Analytical biochemistry, 272(2), 149-155.

Vetri, F., Choudhury, M. S. R., Pelligrino, D. A., & Sundivakkam, P. (2014). BK Ca channels as physiological regulators: a focused review. Journal of Receptor, Ligand and Channel Research, 7, 3-13.

Wu, C., Gopal, K. V., Lukas, T. J., Gross, G. W., & Moore, E. J. (2014). Pharmacodynamics of potassium channel openers in cultured neuronal networks. European journal of pharmacology, 732, 68-75.
How to Cite
Ibrahim, Z. G., & Elrewey, H. A. S. (2020). Rubidium Efflux Assay for the Determination of Calcium Activated Potassium Channel Activity. American International Journal of Biology and Life Sciences, 2(1), 18-27.
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