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Difference between revisions of "Talk:Hydrogenion flux"

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== O2k-Manual ==
== Measurement of proton flux with the O2k-pH ISE-Module ==
=== Introduction and scope ===
 
:::: The [[Oroboros O2k]] supports the modular O2k-MultiSensor extension for recording potentiometric (voltage) signals simultaneously with the oxygen signals in both O2k-chambers. Potentiometric measurements result in a voltage signal ('''pX''') which is  typically a linear function of the logarithm of the activity  (concentration) of the substance of interest (the ''analyte''). A  calibrated pH electrode displays the negative decadic logarithm of the H<sup>+</sup> ion activity (potentia hydrogenii) and thus got its name “pH electrode”. Using a pH / reference electrode module,the extracellular proton flux can either be calculated by changes in pH over time (previous calculation of buffering capacity of the medium required) or by the amount of injected base via pH Stat. MiPNet 16.0x
:::: The [[Oroboros O2k]] supports the modular O2k-MultiSensor extension for recording potentiometric (voltage) signals simultaneously with the oxygen signals in both O2k-chambers. Potentiometric measurements result in a voltage signal ('''pX''') which is  typically a linear function of the logarithm of the activity  (concentration) of the substance of interest (the ''analyte''). A  calibrated pH electrode displays the negative decadic logarithm of the H<sup>+</sup> ion activity (potentia hydrogenii) and thus got its name “pH electrode”. Using a pH / reference electrode module,the extracellular proton flux can either be calculated by changes in pH over time (previous calculation of buffering capacity of the medium required) or by the amount of injected base via pH Stat. MiPNet 16.0x


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== pH-Stat ==
Please note that of course the more straightforward calculation of proton flows from the measured pH slope is also possible while operating in pH-Stat mode!


== Applications  ==
== Applications  ==

Revision as of 12:34, 8 April 2020


high-resolution terminology - matching measurements at high-resolution


Talk:Hydrogenion flux

Description

Volume-specific proton flux is measured in a closed system as the time derivative of proton concentration, expressed in units [pmol·s-1·mL-1]. Proton flux can be measured in an open system at steady state, when any acidification of the medium is compensated by external supply of an equivalent amount of base. The extracellular acidification rate (ECAR) is the change of pH in the incubation medium over time, which is zero at steady state. Volume-specific proton flux is comparable to volume-specific oxygen flux [pmol·s-1·mL-1], which is the (negative) time derivative of oxygen concentration measured in a closed system, corrected for instrumental and chemical background.

pH is the negative logarithm of proton activity. Therefore, ECAR is of interest in relation to acidification issues in the incubation buffer or culture medium. The physiologically relevant metabolic proton flux, however, must not be confused with ECAR.

Abbreviation: JH+

Reference: Gnaiger 2014 MitoPathways

Proton flux versus glycolytic flux

  1. Measured changes in pH over time (ECAR) must be transformed from the logarithmic scale to the linear scale of proton flux.
  2. Measurement of extracellular proton flux and glycolytic flux are related under specifically controlled conditions. Such conditions must be carefully evaluated, may require modifications of protocols, and must be corrected for acid-base reactions unrelated to glycolytic flux.
  3. The measurement of proton flux alone is not sufficient to determine if the origin of the protons is the glycolysis or other sources. For example, the carbon dioxide formed during the mitochondrial respiration acts as a net donor of protons into the media and as consequence has to be taken into account. During the oxidation of the glucose, we have two main metabolic pathways involved and both have a net effect over the proton flux:
400ppx
400ppx
400ppx
As we can observe, the production of protons by oxidative phosphorylation is three times higher than the one produced by the glycolysis per molecule of glucose. However, the chemical rate of production could be used to determine which is the main source of protons in our sample under specific conditions.
  • We have also to take into account the pka for the point of equilibrium of the most common weak acids that will be formed during both processes:


Additional resources

» O2k-Manual: MiPNet23.15 O2k-pH ISE-Module

» O2k-SOP: MiPNet08.16 pH calibration

» MitoPedia O2k and high-resolution respirometry: O2k hardware 



Template NextGen-O2k.jpg


MitoPedia O2k and high-resolution respirometry: O2k-Open Support 



O2k signal and output

  1. O2k signal: The O2k-pH ISE-Module is operated through the pX channel of the O2k, with electric potential (volt [V]) as the primary and raw signal
  2. O2k output: type I and II


pH changes versus glycolytic flux

Measurement of extracellular proton flux and glycolytic flux are related under specifically conrolled conditions. Such conditions must be carefully evaluated, may require modifications of protocols, and need data analysis beyond reporting changes of pH.
  • The extracellular acidification rate (ECAR) is the change of pH over time, which may be of interest in relation to acidification problems in a culture medium or incubation buffer. pH is the negative logarithm of proton activity. Comparable to volume-specific [[oxygen flux] [pmol·s-1·mL-1]], which is the (negative) time derivative of oxygen concentration measured in a closed system, volume-specific proton flux is the time derivative of proton concentration, expressed in units [pmol·s-1·mL-1]]. The physiologically relevant metabolic proton flux, therefore, must not be confused with ECAR.
» Proton flux
  • To accurately measure biologically induced changes in pH, the buffering capacity of the medium has to be small. This may be addressed either by using or preparing media with a buffering capacity that is low but still sufficient to keep the pH in the desired range for a limited period of time. An alternative approach is to use buffers with very low buffering capacity and keep the pH value inside the desired limits by a pH-Stat.


Compare measurement of pH with the pH electrode and ratiometric fluorometric methods (NextGen-O2k)

» Carboxy SNARF 1
» HPTS


Measurement of proton flux with the O2k-pH ISE-Module

The Oroboros O2k supports the modular O2k-MultiSensor extension for recording potentiometric (voltage) signals simultaneously with the oxygen signals in both O2k-chambers. Potentiometric measurements result in a voltage signal (pX) which is typically a linear function of the logarithm of the activity (concentration) of the substance of interest (the analyte). A calibrated pH electrode displays the negative decadic logarithm of the H+ ion activity (potentia hydrogenii) and thus got its name “pH electrode”. Using a pH / reference electrode module,the extracellular proton flux can either be calculated by changes in pH over time (previous calculation of buffering capacity of the medium required) or by the amount of injected base via pH Stat. MiPNet 16.0x













Applications

For simultaneous measurement of O2 and pH, we refer to the classical literature on bioenergetics and the discovery of the chemiosmotic coupling mechanism, the quantification of H+/O2 stoichiometric ratios for proton pumping (Peter Mitchell). Other groups (e.g. SE_Lund_Elmer E) have used the pH electrode in the O2k in conjunction with a study of mitochondrial permeability transition.
The majority of novel applications will address the problem of aerobic glycolysis in intact cells, using the measurement of proton production as an indirect but continuous record of lactate production and corresponding acidification of the medium, while simultaneously monitoring oxygen concentration and oxygen consumption. In a well buffered culture medium, the pH change is extremely small relative to the amount of protons (lactic acid) produced, hence a low-buffering capacity medium needs to be applied. A titration of acid (lactic acid or HCl) into the low-buffering capacity medium yields the pH-dependent buffering capacity (Delta H+ added/Delta H+ measured by the pH electrode). Under various metabolic conditions, lactic acid production is the dominant mechanism causing acidification, hence the pH measurement is a good indirect indicator of aerobic glycolysis.




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References

ChapterSectionLast update
MiPNet07.08 User information
O2k-Manual
O2k-Manual: user information. PLEASE STUDY THIS MANUAL.
2017-11-03
MiPNet19.18 O2k-Series G Core manual
O2k-Manual
O2k-Core manual contents.
2016-08-08
MiPNet19.18B POS-service
O2k-Manual
Service of the polarographic oxygen sensor OroboPOS.
2021-06-23
MiPNet19.18C DatLab 6: Guide
O2k-Manual
DatLab-guide through the menus.
2016-08-24
MiPNet19.18E O2 flux analysis - DatLab 6
O2k-Manual
Oxygen flux analysis: DatLab real-time.
2016-08-08
MiPNet26.06 DatLab 7: Guide
O2k-Manual
DatLab-guide through the menus.
2021-06-02
MiPNet28.10 SmartPOS-service
O2k-Manual
SmartPOS: Service
2023-09-29
Titration-Injection-microPump.jpg
  • TIP2k-Manual***
» O2k-Catalogue: TIP2k
» O2k-Publications: TIP2k
ChapterSectionLast update
MiPNet12.10 TIP2k-manual
O2k-Manual
Titration-Injection microPump TIP2k manual.
2021-07-08



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MitoPedia concepts: MiP concept 


MitoPedia methods: Respirometry, Fluorimetry