Calcium electrode

The OROBOROS ISE system is designed with replaceable membranes so in principal you can measure TPP or Ca.

A Ca2+ membrane with a composition similar to the one described by Simon and coworkers has been tested with the Oroboros ISE system and detection limits of at least 10 nM were achieved in Ca2+ buffered calibration solutions. This membrane is obtainable from Oroboros Instruments on request. There may be further optimizations of the membrane composition to ideally fit the the typical applications of Oroboros customers. However, the main obstacle in establishing useful Ca2+ measurements appears to be not the Ca sensitive membrane but the methodology of its application in an medium simulating intracellular conditions.

Note: The operation of a Ca2+ electrode at typically high extracellular Ca2+ concentrations should be straightforward and devoid of the difficulties described here.

These difficulties include both the calibration of the Ca2+ electrode and the planning of a sensible biological experiment to use it. This is ongoing development therefore Oroboros Instruments offers Ca2+ membranes without scientific support beyond the information on this page, specifically to customers interested in developing a suitable protocol. While this support may grow in the future it will need user innovation and cooperation of users in the World Wide MiPNet to raise this support to the similar high as achieved for respiratory measurements!

Operation of the Ca2+ electrode

General

The general operation (assembly, of the Oroboros ISE system is described in MiPNet15.03.

Calculation of free Ca2+ concentrations

To work at physiological Ca²⁺ concentrations requires usually Ca buffering by chelating agents. The calculation of Ca2+ free in such solutions is quite complicated and the results depend i.a on ionic strength, temperature and very strongly on the solution pH value. Tools for such calculations are available on-line at Chris Pattons MAXCHELATOR Page maxchelator.stanford.edu. Many calculations, published or implemented in programs, depend on a single set of data compiled by . Please note that in spite of the availability of easy to use software tools the calculation of free Ca2+ concentration is an extremely difficult ans - so to speak. daring task. The accuracy of these calculations is severely limited by several factors:

• many underlying thermodynamic constant may not be known precisely
• some additional thermodynamic constants necessary for adequate temperature correction may not be known at all
• it may be difficult to set the experimental parameters pH, temperature, and ionic strength with the necessary precision

Inner filling solution

The following inner filling solution was used: CaCl2: 10 mM

EDTA: 50 mM

pH adjusted to 8.5 with KOH

Conditioning

is a controversial topic. If any conditioning is done, the used Ca concentration should probable not be much higher than the highest expected concentration during use of the electrode.

Calibration

As a potentiometer method the ca2+ electrode will deliver a signal that is (for the working range) linear to the logarithm of the free ca2+ concentration. Therefore, the electrode is calibrated by plotting Electrode signal vs. logarithm of the free Ca2+ concentration. Calibration of the Ca2+ electrode at low (< 1µM) Ca2+ levels is typically done by exposing the electrode to a series of Ca2+ calibration buffers. Each calibration solution typically contains a Ca2+ chelating agent, a pH buffer, CaCl2, and a salt (KCl) to adjust ionic strength. For suggested compositions see the literature in the reading list below. Examples from the literature may then be adapted to individual need using the software tools mentioned above. The pH of all solutions have to be adjusted very carefully! For calibrations spanning a large (several orders of magnitude) range of free Ca2+ concentrations it will be necessary to use calibration buffers with quite different compositions. The non linearity of the electrode response seen in such calibrations may be mainly due to the difficulties in calculating the free Ca2+ concentration.

Use in a biological experiment

You could help us in the development by explaining what you would like to do/ see in a Ca²⁺ experiment and what you expect from the electrode: what ca concentrations do you want to measure, Ca²⁺ release or uptake? what total concentration change in a 2 ml chamber (!) do you expect? Do you want to measure in a Ca buffered medium? (decreased sensitivity to changes) or without Ca²⁺ buffering but then how do you get to physiological Ca²⁺ concentration? Do you want to measure at physiological Ca²⁺ concentrations?.......

Reading list

We have complied a short reading list that may be of interest to those planing to to do Ca²⁺ measurements. A special emphasis are references describing the preparation of Ca²⁺ calibration buffers.

Ca measurement reading list

References

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