Premium
Calibration and characterization of intracellular Asante Potassium Green probes, APG‐2 and APG‐4
Author(s) -
Rana Priyanka S.,
Gibbons Brandon A.,
Alexy Vereninov A.,
Yurinskaya Valentina E.,
Clements Robert,
Model Timothy M.,
Model Michael A.
Publication year - 2019
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2019.33.1_supplement.707.4
Subject(s) - nigericin , potassium , intracellular , valinomycin , biophysics , chemistry , ouabain , fluorescence , extracellular , membrane potential , sodium , analytical chemistry (journal) , biochemistry , chromatography , membrane , biology , physics , organic chemistry , quantum mechanics
The response of fluorescent ion probes to ions is affected by intracellular environment. To properly calibrate them, intracellular concentration of the measured ion must be made equal to its extracellular concentration. In the first, computational, part of this work, we show, using the example of potassium, that the two requirements for ion equilibration are complete dissipation of membrane potential and high membrane permeability for both potassium and sodium. In the second part, we tested the ability of various ionophores to achieve potassium equilibration in Jurkat and U937 cells and found a combination of valinomycin, nigericin, gramicidin and ouabain to be the most effective. In the third part, we applied this protocol to two Asante Potassium Green probes, APG‐4 and APG‐2. APG‐4 shows good sensitivity to potassium but its fluorescence is sensitive to protein density; therefore, calibration buffer had to be supplemented with 50 mM sucrose to keep cell volume constant. With these precautions taken, the average potassium concentrations in U937 and Jurkat cells were measured as 132 mM and 118 mM, respectively. The other tested probe, APG‐2, is non‐selective for cations; this is, however, a potentially useful property because the sum [K + ] + [Na + ] determines the amount of intracellular water. Support or Funding Information The research was partly supported by the Kent State University Research Council (MM) and by the Russian Fedration grant 0124‐2018‐0003 (VY and AV) This abstract is from the Experimental Biology 2019 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .