Respiratory state: Difference between revisions
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|description='''Respiratory states''' of mitochondrial preparations and | |description='''Respiratory states''' of [[Mitochondrial preparations|mitochondrial preparations]] and [[Living cells|living cells]] are defined in the current literature in many ways and with a diversity of terms. Mitochondrial respiratory states must be defined in terms of both, the [[coupling control state]] and the [[electron transfer-pathway state]]. | ||
|info=[[Gnaiger 2014 MitoPathways]] | |info=[[Gnaiger 2014 MitoPathways]] | ||
}} | }} | ||
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::::* [[OXPHOS]], [[LEAK]], [[ETS]] (''P, L, E'') - corrected for [[ROX]]. ''CCR'': ''[[L/E]]'', ''[[P/E]]'', ''[[L/P]]'' | ::::* [[OXPHOS]], [[LEAK]], [[ETS]] (''P, L, E'') - corrected for [[ROX]]. ''CCR'': ''[[L/E]]'', ''[[P/E]]'', ''[[L/P]]'' | ||
::: Coupling states of | ::: Coupling states of living cells: | ||
::::* [[ROUTINE]], [[LEAK]], [[ETS]] (''R, L, E'') - corrected for [[ROX]]. ''CCR'': ''[[L/E]]'', ''[[R/E]]'', ''[[L/R]]'' | ::::* [[ROUTINE]], [[LEAK]], [[ETS]] (''R, L, E'') - corrected for [[ROX]]. ''CCR'': ''[[L/E]]'', ''[[R/E]]'', ''[[L/R]]'' | ||
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:::: Electron transfer-pathway state, ''[[PCS]]'', are defined by substrate type (at saturating concentration): | :::: Electron transfer-pathway state, ''[[PCS]]'', are defined by substrate type (at saturating concentration): | ||
::::* | ::::* Living cells: [[endogenous]], [[exogenous]] substrate control | ||
::::* Mitochondrial preparations: specific substrate-inhibitor combinations for selectively stimulating electron entry though Complex I, CII, or other branches converging at the Q-junction, particularly with [[fatty acid oxidation]], alpha-[[glycerophosphate]], ([[Complex I-linked substrate state]], [[Complex II-linked substrate state]], etc.), or substrate combinations applied for reconstitution of [[TCA cycle]] function (e.g. [[Complex I&II-linked substrate state]], etc.). | ::::* Mitochondrial preparations: specific substrate-inhibitor combinations for selectively stimulating electron entry though Complex I, CII, or other branches converging at the Q-junction, particularly with [[fatty acid oxidation]], alpha-[[glycerophosphate]], ([[Complex I-linked substrate state]], [[Complex II-linked substrate state]], etc.), or substrate combinations applied for reconstitution of [[TCA cycle]] function (e.g. [[Complex I&II-linked substrate state]], etc.). | ||
Revision as of 08:27, 23 April 2020
Description
Respiratory states of mitochondrial preparations and living cells are defined in the current literature in many ways and with a diversity of terms. Mitochondrial respiratory states must be defined in terms of both, the coupling control state and the electron transfer-pathway state.
Reference: Gnaiger 2014 MitoPathways
MitoPedia concepts:
MiP concept,
Respiratory state,
SUIT concept,
Recommended
MitoPedia methods:
Respirometry,
Spectrophotometry
MitoPedia topics:
EAGLE
Communicated by Gnaiger E 2010-10-21, edited 2016-08-26.
Coupling control states
- Coupling states and CCR of mitochondrial preparations:
- Coupling states of living cells:
Electron transfer-pathway state
- Electron transfer-pathway state, PCS, are defined by substrate type (at saturating concentration):
- Living cells: endogenous, exogenous substrate control
- Mitochondrial preparations: specific substrate-inhibitor combinations for selectively stimulating electron entry though Complex I, CII, or other branches converging at the Q-junction, particularly with fatty acid oxidation, alpha-glycerophosphate, (Complex I-linked substrate state, Complex II-linked substrate state, etc.), or substrate combinations applied for reconstitution of TCA cycle function (e.g. Complex I&II-linked substrate state, etc.).
- Control by substrate concentration: Kinetic control states:
- Kinetic substrate or adenylate control: Kinetic studies with variation of a specific substrate (reduced substrate supplying electrons to the ETS; ADP, Pi; O2; cytochrome c) are analyzed by kinetic functions (e.g. hyperbolic), yielding apparent kinetic constants, such as Jmax, Km', c50, or p50.
- Kinetic inhibitor control: Kinetic studies with variation of a specific inhibitor yield apparent kinetic constants, such as the KI'.
Classical respiratory states
- Chance and Williams (1955):
- Derived respiratory states:
- Thermodynamics of irreversible processes:
MitoPedia: Respiratory states
- ยป See the complete MitoPedia: Respiratory states
- ยป MitoPedia: SUIT