Cytochrome c

high-resolution terminology - matching measurements at high-resolution

Cytochrome c

Description

Cytochrome c is a component of the electron transfer system (ETS) 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. [1].

Abbreviation: c

Reference: MiPNet09.12; Gnaiger 2002 Biochem Soc Trans

MitoPedia topics: Substrate and metabolite 

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 = 12500.

Preparation of 4 mM cytochrome c solution (dissolved in H₂O):

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.

Caution: Chemicals stored in the fridge or freezer should be allowed to reach room temperature before opening.

Oxygraph-2k manual titrations: MiPNet09.12 O2k-Titrations

• Titration volume: 5 µl using a 25 µl syringe (2 ml O2k-chamber)
• Final concwentration: 10 µM

Gnaiger E (2014) Cytochrome c control: a test for outer mt-membrane integrity. Mitochondr Physiol Network 2014-04-21.

OROBOROS (2014) Mitochondr Physiol Network

Abstract: The cytochrome c control factor, (J_CHOc-J_CHO)/J_CHOc, provides an index for the outer mt-membrane integrity.

• O2k-Network Lab: AT Innsbruck Gnaiger E

Labels:

HRR: Theory 

Cytochrome c control: a test for outer mt-membrane integrity

Outer mitochondrial membrane damage can be evaluated by stimulation of respiration by exogenously added cytochrome c.

Determination of cytochrome c loss

Adding cytochrome c (10 µM) to stimulate respiratory activity provides an estimate of cytochrome c loss. In general, maximum respiratory activity is obtained under conditions of saturating substrate concentrations and system dependent in the coupled (ADP stimulated) State P or noncoupled (uncoupler stimulated) State E.

Cytochrome c test

When using cytochrome c as a quality control for permeabilised muscles from various species, which cytochrome c should we use (a wide range of types of cytochrome c is available from Sigma-Aldrich) and at which concentration?

We apply routinely cytochrome c from Sigma C 7752. It would be interesting to compare the consequence of application of different sources of cytochrome c.

In a detailed discussion on the dependence of respiration in isolated mitochondria and permeabilized cardiac fibers, we showed for the first time showing that cytochrome c kinetics is different when studying a segment of the ETS (CII-linked: succinate+rotenone) versus the isolated step of cytochrome c oxidase (CIV; ascorbate+TMPD+antimycin A). For CII-linked respiration, an exernal cytochrome c concentration of 10 µM yields kinetic saturation (monophasic hyperbolic), but kinetics is biphasic for CIV and 10 µM is not saturating.,

Importantly, cytochrome c increases the chemical background oxygen flux in the presence of ascorbate and TMPD, dependent on oxygen concentration and cytochrome c concentration, and appropriate chemical background corrections are required., Without ascorbate and TMPD, added cytochrome c is stable.

Evaluation of the cytochrome c effect, when respiration is slightly unstable: Mark respiration just before cytochrome c addition and after. Take these to values to calculate the increase of respiration due to cytochrome c addition.

At which step of the protocol should cytochrome c be added?

If a stimulatory effect of cytochrome c is observed, respiratory capacities measured before cytochrome c addition might be cytochrome c limited and therefore underestimated. This provides an argument to add cytochrome c at an early state of the protocol.

It is important not to add cytochrome c in a LEAK state: There is always an unexplained activation of respiration, unrelated to the injury of the outer mt-membrane. Add cytochrome c only after activation by ADP.

Cytochrome c release

Cytochrome c release induced by sample preparation

A preparation induced damage of the outer mitochondrial membrane and as a result subsequent loss of cytochrome c can be detected by a stimulation of respiration after the addition of cytochrome c. The preparation induced damage can also affect the respiratory complexes. Therefore, experimental runs showing a preparation induced cytochrome c release should be excluded from the final data set. In perfectly prepared muscle fibers cytochrome c should have no stimulatory effect on maximum respiratory activity, in liver biopsies a small effect is observed, even in carefully prepared samples.

Cytochrome c release induced by treatment

Treatment-triggered cytochrome c release, e.g. cell death induction, has to be distinguished from preparation induced damage. If cytochrome c is released as a result of apoptosis induction, this is a biological phenomenon and a relevant result.