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Difference between revisions of "Cytochrome c"

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{{MitoPedia
{{MitoPedia
|abbr=c
|abbr=c
|description='''Cytochrome ''c''''' is a component of the Electron transfer-pathway ([[Electron transfer pathway]]) in mitochondria. It is a small heme protein loosely associated with the outer side of the inner mitochondrial membrane. The heme group of cytochrome ''c'' transfers electrons from [[Complex III]] to [[Complex IV]]. The release of cytochrome ''c'' into the cytoplasm is associated with apoptosis. Cytochrome ''c'' is applied in [[HRR]] to test the integrity of the [[mitochondrial outer membrane]] ([[cytochrome c control factor]]).
|description='''Cytochrome ''c''''' is a component of the Electron transfer-pathway ([[Electron transfer pathway]]) in mitochondria. It is a small heme protein loosely associated with the outer side of the inner mitochondrial membrane. The heme group of cytochrome ''c'' transfers electrons from [[Complex III]] to [[Complex IV]]. The release of cytochrome ''c'' into the cytoplasm is associated with apoptosis. Cytochrome ''c'' is applied in [[HRR]] to test the integrity of the [[mitochondrial outer membrane]] ([[cytochrome c control efficiency]]).
|info=[[MiPNet09.12]]; [[Gnaiger 2002 Biochem Soc Trans]]
|info=[[MiPNet09.12]]; [[Gnaiger 2002 Biochem Soc Trans]]
}}
}}
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== DatLab oxygen flux: performance and data analysis ==
== DatLab oxygen flux: performance and data analysis ==


:::: Quality of the results are strongly affected by the performance and data analysis. By adding cytochrome ''c'' in respirometric experiments the outer mitochondrial membrane integrity can be evaluated ([[Cytochrome c control factor|cytochrome ''c'' control factor]]). The following DatLab traces illustrate examples of cytochrome ''c'' addition:
:::: Quality of the results are strongly affected by the performance and data analysis. By adding cytochrome ''c'' in respirometric experiments the outer mitochondrial membrane integrity can be evaluated ([[Cytochrome c control efficiency|cytochrome ''c'' control efficiency]]). The following DatLab traces illustrate examples of cytochrome ''c'' addition:


<gallery mode=default perrow=2 widths="600px" heights="400px">
<gallery mode=default perrow=2 widths="600px" heights="400px">
File:cyt_c_traces_O2_flux_01.png | '''Figure 1'''. Cytochrome ''c'' addition (2c) in OXPHOS state, using pyruvate and malate as NADH-linked substrates. An increase in oxygen flux per volume (red trace, right axis) can be seen upon cytochrome ''c'' addition ([[Cytochrome c control factor|cytochrome ''c'' control factor]]=0.09). Cardiac isolated mitochondria from mouse. Experiment 2019-02-19 P1-02 ([[SUIT-008_O2_mt_D026|SUIT-008 O2 mt D026]], DatLab 7.4).
File:cyt_c_traces_O2_flux_01.png | '''Figure 1'''. Cytochrome ''c'' addition (2c) in OXPHOS state, using pyruvate and malate as NADH-linked substrates. An increase in oxygen flux per volume (red trace, right axis) can be seen upon cytochrome ''c'' addition ([[Cytochrome c control efficiency|cytochrome ''c'' control efficiency]]=0.09). Cardiac isolated mitochondria from mouse. Experiment 2019-02-19 P1-02 ([[SUIT-008_O2_mt_D026|SUIT-008 O2 mt D026]], DatLab 7.4).


File:cyt_c_traces_O2_flux_02.png | '''Figure 2'''. Example of cytochrome ''c'' addition (2c) in  OXPHOS state, in the presence of pyruvate and malate as NADH-linked substrates. The ([[Cytochrome c control factor|cytochrome ''c'' control factor]]=0.02) indicates that cryopreservation, sample preparation and the use of the detergent [[Digitonin|digitonin]] did not affect the integrity of the outer mitochondrial membrane. Cryopreserved HEK-293 cells. Experiment 2017-02-08 P1-02 ([[SUIT-008_O2_ce-pce_D025|SUIT-008 O2 ce-pce D025]], DatLab 7.4).
File:cyt_c_traces_O2_flux_02.png | '''Figure 2'''. Example of cytochrome ''c'' addition (2c) in  OXPHOS state, in the presence of pyruvate and malate as NADH-linked substrates. The ([[Cytochrome c control efficiency|cytochrome ''c'' control efficiency]]=0.02) indicates that cryopreservation, sample preparation and the use of the detergent [[Digitonin|digitonin]] did not affect the integrity of the outer mitochondrial membrane. Cryopreserved HEK-293 cells. Experiment 2017-02-08 P1-02 ([[SUIT-008_O2_ce-pce_D025|SUIT-008 O2 ce-pce D025]], DatLab 7.4).


File:cyt_c_traces_O2_flux_03.png | '''Figure 3'''. Cytochrome ''c'' addition (2c) in  OXPHOS state (in the presence of pyruvate, glutamate and malate) triggers an increase of the oxygen flux. This high [[Cytochrome c control factor|cytochrome ''c'' effect]] (0.44) may indicate a lost of the outer mitochondrial membrane integrity due to 1) sample preparation or 2) treatment (see [[Cytochrome_c_control_factor#Cytochrome_c_release|cytochrome ''c'' release]]). BAT tissue homogenate from mouse. Experiment 2015-07-09-P2-03.
File:cyt_c_traces_O2_flux_03.png | '''Figure 3'''. Cytochrome ''c'' addition (2c) in  OXPHOS state (in the presence of pyruvate, glutamate and malate) triggers an increase of the oxygen flux. This high [[Cytochrome c control efficiency|cytochrome ''c'' effect]] (0.44) may indicate a lost of the outer mitochondrial membrane integrity due to 1) sample preparation or 2) treatment (see [[Cytochrome c control efficiency#Cytochrome_c_release|cytochrome ''c'' release]]). BAT tissue homogenate from mouse. Experiment 2015-07-09-P2-03.


File:2019-08-06 P3-02 - A - for cyt c page.png | '''Figure 4'''. Cytochrome ''c'' addition (1c) in  OXPHOS state (in the presence of succinate and rotenone) seems to trigger at first a decrease in oxygen flux, and then an increase up to the same levels as before. It is important to wait for the stabilization of the oxygen flux to set the mark, avoiding an artefactual negative [[Cytochrome c control factor|cytochrome ''c'' effect]] (in this case, the cytochrome c control factor was 0.001). Huh 7 cells, permeabilized with digitonin. Experiment 2019-08-06 P3-02.
File:2019-08-06 P3-02 - A - for cyt c page.png | '''Figure 4'''. Cytochrome ''c'' addition (1c) in  OXPHOS state (in the presence of succinate and rotenone) seems to trigger at first a decrease in oxygen flux, and then an increase up to the same levels as before. It is important to wait for the stabilization of the oxygen flux to set the mark, avoiding an artefactual negative [[Cytochrome c control efficiency|cytochrome ''c'' effect]] (in this case, the cytochrome ''c'' control efficiency was 0.001). Huh 7 cells, permeabilized with digitonin. Experiment 2019-08-06 P3-02.


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::: See also: [[Steady_state#OXPHOS_state|Steady state]], Figures 1-3.
::: See also: [[Steady_state#OXPHOS_state|Steady state]], Figures 1-3.
::::* ''For further information see:'' » [[Cytochrome c control factor]]
::::* ''For further information see:'' » [[Cytochrome c control efficiency]]





Revision as of 09:56, 13 November 2020


high-resolution terminology - matching measurements at high-resolution


Cytochrome c

Description

Cytochrome c is a component of the Electron transfer-pathway (Electron transfer pathway) in mitochondria. It is a small heme protein loosely associated with the outer side of the inner mitochondrial membrane. The heme group of cytochrome c transfers electrons from Complex III to Complex IV. The release of cytochrome c into the cytoplasm is associated with apoptosis. Cytochrome c is applied in HRR to test the integrity of the mitochondrial outer membrane (cytochrome c control efficiency).

Abbreviation: c

Reference: MiPNet09.12; Gnaiger 2002 Biochem Soc Trans

Application in HRR: storage and stock solution of c

c: Cytochrome c (from equine heart), Sigma C 7752, 50 mg, store at -20 °C; FW = 12384 Da.
Caution: Chemicals stored in the fridge or freezer should be allowed to reach room temperature before opening.


Preparation of 4 mM cytochrome c solution (dissolved in H2O) for 2-mL O2k-chamber:
  1. Weigh 50 mg cytochrome c into a small glass beaker. Difficult to weigh, since the powder is electromagnetic.
  2. Add 1 mL H2O; c dissolves easily.
  3. Divide into 0.2 mL portions.
  4. Store at -20 °C.
» O2k manual titrations: MiPNet09.12 O2k-Titrations
  • Titration volume (2-mL O2k-chamber): 5 µL using a 25 µL Hamilton syringe.
  • Final concentration: 10 µM.


Preparation of 5 mM cytochrome c solution (dissolved in H2O) for 0.5-mL O2k-chamber:
  1. Weigh 62,5 mg cytochrome c into a small glass beaker. Difficult to weigh, since the powder is electromagnetic.
  2. Add 1 mL H2O; c dissolves easily.
  3. Divide into 0.2 mL portions.
  4. Store at -20 °C.
» O2k manual titrations: MiPNet09.12 O2k-Titrations
  • Titration volume (0.5-mL O2k-chamber): 1 µL using a 10 µL Hamilton syringe.
  • Final concentration: 10 µM.


DatLab oxygen flux: performance and data analysis

Quality of the results are strongly affected by the performance and data analysis. By adding cytochrome c in respirometric experiments the outer mitochondrial membrane integrity can be evaluated (cytochrome c control efficiency). The following DatLab traces illustrate examples of cytochrome c addition:
See also: Steady state, Figures 1-3.



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SUITbrowser question: mt outer membrane integrity

The cytochrome c test is available at several SUIT protocols. The SUITbrowser shows which protocols contain this test, alongside answer other research questions.




MitoPedia topics: Substrate and metabolite