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

Difference between revisions of "Cell ergometry"

From Bioblast
Line 17: Line 17:
== Figure 1: Phosphorylation control protocol in the intact cell ==
== Figure 1: Phosphorylation control protocol in the intact cell ==


# [[Biochemical coupling efficiency]]: ''j<sub>E-L</sub>'' = (''E-L'')/''E''
# [[ETS coupling efficiency]]: ''j<sub>≈E</sub>'' = ''≈E/E'' = (''E-L'')/''E''
# [[ETS excess factor over R |ETS excess factor over ''R'']]: ''Ex<sub>R</sub>/E'' = (''E-R'')/''E''
# [[ETS excess factor over R |ETS excess factor over ''R'']]: ''Ex<sub>R</sub>/E'' = (''E-R'')/''E''
# [[ROUTINE phosphorylation control factor]]: ''≈R/R'' = (''R-L'')/''R''
# [[ROUTINE phosphorylation control factor]]: ''j<sub>≈R</sub>'' = ''≈R/R'' =(''R-L'')/''R''
# [[ROUTINE phosphorylation control ratio]]: ''≈R/E'' = (''R-L'')/''E''
# [[ROUTINE phosphorylation control ratio]]: ''≈R/E'' = (''R-L'')/''E''



Revision as of 22:34, 25 August 2014


high-resolution terminology - matching measurements at high-resolution


Cell ergometry

Description

Biochemical cell ergometry aims at measurement of JO2,max (compare VO2,max in exercise ergometry of humans and animals) of cell respiration linked to phosphorylation of ADP to ATP. The corresponding OXPHOS capacity is based on saturating concentrations of ADP, [ADP]*, and inorganic phosphate, [Pi]*, available to the mitochondria. This is metabolically opposite to uncoupling respiration, which yields ETS capacity. The OXPHOS state can be established experimentally by selective permeabilization of cell membranes with maintenance of intact mitochondria, titrations of ADP and Pi to evaluate kinetically saturating conditions, and establishing fuel substrate combinations which reconstitute physiological TCA cycle function.

Abbreviation: n.a.

Reference: Gnaiger 2014 MitoPathways


MitoPedia methods: Respirometry 


MitoPedia topics: "Respiratory state" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property. Respiratory state"Respiratory state" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property. 

960px High-resolution pdf: »File:OROBOROS Poster HRR.pdf

OXPHOS ETS ROUTINE LEAK - ROX

Figure 1: Phosphorylation control protocol in the intact cell

  1. ETS coupling efficiency: j≈E = ≈E/E = (E-L)/E
  2. ETS excess factor over R: ExR/E = (E-R)/E
  3. ROUTINE phosphorylation control factor: j≈R = ≈R/R =(R-L)/R
  4. ROUTINE phosphorylation control ratio: ≈R/E = (R-L)/E


Ergometry

VO2max or VO2peak in cycle or treadmill ergometry is expressed in units of [ml O2·min-1·kg-1] body mass. 1 ml oxygen at STPD is equivalent to 22.392 mmol O2. Therefore, multiply by 1000/(22.392·60) to convert VO2peak to JO2peak expressed in SI units [pmol·s-1·mg-1]:

1 ml O2·min-1·kg-1 = 0.744 µmol·s-1·kg-1

VO2peak (JO2peak) typically declines from 70 to 25 ml O2·min-1·kg-1 (50 to 20 µmol·s-1·kg-1) in the range of healthy trained to obese untrained humans.