Complex IV: Difference between revisions

From Bioblast
No edit summary
No edit summary
Β 
(49 intermediate revisions by 8 users not shown)
Line 1: Line 1:
{{MitoPedia
{{MitoPedia
|abbr=CIV
|abbr=CIV
|description='''Cytochrome c oxidase''' or '''Complex IV''' is the terminal oxidase of the mitochondrial [[ETS]], reducing oxygen to water, with reduced [[cytochrome c]] as a substrate. CIV is frequently abbreviated as COX or CcO.Β  It is the 'ferment' (Atmungsferment) of Otto Warburg, shown to be related to the cytochromes by David Keilin.
|description='''Complex IV''' or '''cytochrome ''c'' oxidase''' is the terminal oxidase of the mitochondrial [[electron transfer system]], reducing [[oxygen]] to [[water]], with reduced [[cytochrome c |cytochrome ''c'']] as a substrate. Concomitantly to that, CIV [[Proton pump|pumps protons]] against the electrochemical protonmotive force. CIV is frequently abbreviated as COX or CcO.Β  It is the 'ferment' (Atmungsferment) of Otto Warburg, shown to be related to the cytochromes discovered by David Keilin.
|type=Enzyme
|info=[[MiPNet06.06]], [[Gnaiger 2020 BEC MitoPathways]]
}}
}}
__TOC__
== HRR protocol: Complex IV assay ==
::::Electron flow through [[Complex IV]] (CIV / cytochrome ''c'' oxidase, COX) is measured in intact mitochondria after inhibition of [[Complex III]] by [[antimycin A]] and addition of tetramethyl-p-phenylenediamine [[TMPD]] (Tm) and [[ascorbate]] (As). Correction for autooxidation of [[TMPD]] and [[ascorbate]], which is strongly oxygen-dependent, is a routine procedure in high-resolution respirometry. For that we recommend the evaluation of chemical background using inhibitors of CIV (such as [[cyanide]], [[azide]]) after ascorbate and TMPD titrations.
::::CIV-linked '''respiration''' can be measured in different coupling states ([[LEAK|''L'']], [[OXPHOS|''P'']], and [[ET-capacity|''E'']]). Since CIV is a [[proton pump]] of the [[electron transfer system]], measurement of '''CIV activity''' requires [[uncoupler]] titrations to eliminate any potential control by the phosphorylation system. [[cytochrome c|Cytochrome ''c'']] addition is also recommended to avoid any limitation by cytochrome ''c'' release.
=== Ascorbate and TMPD ===
:::: [[Ascorbate]] (As; 2 mM) and [[TMPD]] (Tm; 0.5 mM) are added to [[mitochondrial preparations]]. TMPD is a CIV-specific electron donor, while ascorbate ensures that the TMPD is reduced and continues to donate electrons to build a linear rate of CIV activity. After sequential titration of ascorbate and TMPD (with or without added cytochrome ''c'' - autooxidation is higher in the presence of cytochrome ''c''.), the total oxygen flux increases due to (i) CIV activity and (ii) autooxidation of ascorbate and TMPD as a function of oxygen pressure. It is important to '''add ascorbate before TMPD''' to avoid uncontrollable autoxidation.Β 
:::: Cytochrome ''c'' oxidase (CIV) in intact mitochondria has a biphasic kinetics for TMPD ([[Gnaiger_2002_Biochem_Soc_Trans]]).Β  Due to the high ''K''<nowiki>'</nowiki><sub>m</sub> of the low-affinity phase, TMPD cannot be added at saturating concentrations, since then autoxidation of TMPD would be strikingly high.Β  The actually chosen TMPD concentration, therefore, is a compromise. Comparison of [[electron transfer pathway]] pathway flux versus the single step of CIV with inhibitor titrations with [[cyanide]] or [[azide]] reveal an apparent excess capacity of CIV. The optimum TMPD concentration, therefore, is adjusted to obtain a reaction velocity corresponding to the apparent excess capacity ([[Gnaiger_1998_J Exp Biol]]).
::::Cyanide cannot be used when pyruvate is titrated because it inhibits [[cyanide]] at high oxygen levels (see [[Cyanide]]).
=== Correction for chemical O<sub>2</sub> background ===
:::: After full inhibition of CIV the autooxidation effect is responsible for the remaining oxygen flux.Β  For CIV activity determination, the signal derived from this autooxidation is subtracted from the oxygen flux measured before CIV inhibition. This provides a complete internal calibration of the chemical background, as a function of oxygen concentration.
:::: The oxygen dependence is linear above c. 50 Β΅M O<sub>2</sub>, but biphasic (linear + hyperbolic) below 50 Β΅M O<sub>2</sub>. If you maintain oxygen in the linear dependence above 50 Β΅M, you can use the automatic instrumental background correction in DatLab to also take care of the chemical background correction (in the β€˜Edit Experiment’ window the instrumental background parameters are replaced by the combined background parameters).
=== References ===
::::* O2k-Procedure: [[MiPNet06.06 Chemical O2 background]]
:::: Publications:
::::* Living cells are inadequate for CIV measurement with As+Tm - use permeabilized cells: [[Renner_2002_Mol_Biol_Rep]], [[Renner_2003_Biochim_Biophys_Acta]]
::::* Isolated mitochondria: [[Gnaiger_2002_Biochem_Soc_Trans]]
::::* Permabilized fibers: [[Kuznetsov_2004_Am_J_Physiol_Heart_Circ_Physiol]], [[Lemieux_2011_Int_J_Biochem_Cell_Biol]]
== [[SUITbrowser]] question: CIV ==
:::: The [https://suitbrowser.oroboros.at/ SUITbrowser] can be used to find SUIT protocols to assess CIV activity, alongside answering other research questions.
= List of publications: Complex IV;cytochrome c oxidase =
{{Template:Publications: Complex IV single step}}
{{Template:Abstracts: Complex IV single step}}
{{MitoPedia topics
{{MitoPedia topics
|mitopedia topic=Enzyme
|mitopedia topic=Enzyme
|type=Enzyme
}}
}}

Latest revision as of 13:23, 5 March 2021


high-resolution terminology - matching measurements at high-resolution


Complex IV

Description

[[Description::Complex IV or cytochrome c oxidase is the terminal oxidase of the mitochondrial electron transfer system, reducing oxygen to water, with reduced cytochrome c as a substrate. Concomitantly to that, CIV pumps protons against the electrochemical protonmotive force. CIV is frequently abbreviated as COX or CcO. It is the 'ferment' (Atmungsferment) of Otto Warburg, shown to be related to the cytochromes discovered by David Keilin.]]

Abbreviation: Has abbr::CIV

Reference: [[Info::MiPNet06.06, Gnaiger 2020 BEC MitoPathways]]

HRR protocol: Complex IV assay

Electron flow through Complex IV (CIV / cytochrome c oxidase, COX) is measured in intact mitochondria after inhibition of Complex III by antimycin A and addition of tetramethyl-p-phenylenediamine TMPD (Tm) and ascorbate (As). Correction for autooxidation of TMPD and ascorbate, which is strongly oxygen-dependent, is a routine procedure in high-resolution respirometry. For that we recommend the evaluation of chemical background using inhibitors of CIV (such as cyanide, azide) after ascorbate and TMPD titrations.
CIV-linked respiration can be measured in different coupling states (L, P, and E). Since CIV is a proton pump of the electron transfer system, measurement of CIV activity requires uncoupler titrations to eliminate any potential control by the phosphorylation system. Cytochrome c addition is also recommended to avoid any limitation by cytochrome c release.

Ascorbate and TMPD

Ascorbate (As; 2 mM) and TMPD (Tm; 0.5 mM) are added to mitochondrial preparations. TMPD is a CIV-specific electron donor, while ascorbate ensures that the TMPD is reduced and continues to donate electrons to build a linear rate of CIV activity. After sequential titration of ascorbate and TMPD (with or without added cytochrome c - autooxidation is higher in the presence of cytochrome c.), the total oxygen flux increases due to (i) CIV activity and (ii) autooxidation of ascorbate and TMPD as a function of oxygen pressure. It is important to add ascorbate before TMPD to avoid uncontrollable autoxidation.
Cytochrome c oxidase (CIV) in intact mitochondria has a biphasic kinetics for TMPD (Gnaiger_2002_Biochem_Soc_Trans). Due to the high K'm of the low-affinity phase, TMPD cannot be added at saturating concentrations, since then autoxidation of TMPD would be strikingly high. The actually chosen TMPD concentration, therefore, is a compromise. Comparison of electron transfer pathway pathway flux versus the single step of CIV with inhibitor titrations with cyanide or azide reveal an apparent excess capacity of CIV. The optimum TMPD concentration, therefore, is adjusted to obtain a reaction velocity corresponding to the apparent excess capacity (Gnaiger_1998_J Exp Biol).
Cyanide cannot be used when pyruvate is titrated because it inhibits cyanide at high oxygen levels (see Cyanide).

Correction for chemical O2 background

After full inhibition of CIV the autooxidation effect is responsible for the remaining oxygen flux. For CIV activity determination, the signal derived from this autooxidation is subtracted from the oxygen flux measured before CIV inhibition. This provides a complete internal calibration of the chemical background, as a function of oxygen concentration.
The oxygen dependence is linear above c. 50 Β΅M O2, but biphasic (linear + hyperbolic) below 50 Β΅M O2. If you maintain oxygen in the linear dependence above 50 Β΅M, you can use the automatic instrumental background correction in DatLab to also take care of the chemical background correction (in the β€˜Edit Experiment’ window the instrumental background parameters are replaced by the combined background parameters).

References

Publications:


SUITbrowser question: CIV

The SUITbrowser can be used to find SUIT protocols to assess CIV activity, alongside answering other research questions.


List of publications: Complex IV;cytochrome c oxidase


Questions.jpg


Click to expand or collaps
Β»Publications: Complex IV single step
Publications in the MiPMap
Sort in ascending/descending order by a click on one of the small symbols in squares below.
Default sorting: chronological. Empty fields appear first in ascending order. 

{{#ask: Pathways::CIV |?Was published in year=Year |?Has title=Reference |?Coupling states=Coupling |?Pathways=Pathway |?Preparation=Preparation |?Mammal and model=Organism |?Tissue and cell=Tissue;cell |format=broadtable |limit=5000 |offset=0 |sort=Was published in year |order=descending }}


Questions.jpg


Click to expand or collaps
Β»Abstracts: Complex IV single step
Publications in the MiPMap
Sort in ascending/descending order by a click on one of the small symbols in squares below.

{{#ask: Pathways::CIV |?Was submitted in year=Year |?Has title=Reference |?Coupling states=Coupling |?Pathways=Pathway |?Preparation=Preparation |?Mammal and model=Organism |?Tissue and cell=Tissue;cell |format=broadtable |limit=5000 |offset=0 |sort=Was submitted in year |order=descending }}


MitoPedia topics: Enzyme 

Cookies help us deliver our services. By using our services, you agree to our use of cookies.