Publication | Open Access
The Influence of Respiration and ATP Hydrolysis on the Proton‐Electrochemical Gradient across the Inner Membrane of Rat‐Liver Mitochondria as Determined by Ion Distribution
715
Citations
19
References
1974
Year
BioelectrochemistryIon DistributionMitochondrial BiologyInner MembraneBioenergeticsMembrane TransportMitochondrial StructureAtp HydrolysisBiophysicsHealth SciencesBiochemistryMitochondrial DynamicIon ChannelsMembrane BiologyMembrane PotentialEnergy MetabolismMitochondrial FunctionPhysiologyMg Mitochondrial ProteinMitochondrial MedicineElectrophysiologyCellular BiochemistryMetabolismMedicine
A technique is described to simultaneously estimate the membrane potential and pH gradient across the inner membrane of rat‑liver mitochondria using the distribution of rubidium, acetate, and methylammonium ions. The method employs less than 0.5 mg of mitochondrial protein, is independent of electrode interferences, and its sensitivity to pH gradient versus membrane potential depends on the availability of electrophoretically and electroneutrally translocatable species. The technique measured Δp values of 228 mV (state 4), 170 mV (state 3), and –0.6 mV with rotenone/uncoupler; in sucrose medium it gave +85 mV membrane potential and +1.46 pH gradient; ATP hydrolysis produced an optimal Δp of 220 mV; proton conductance increased above 200 mV; and extra‑mitochondrial phosphate potential tracked Δp but exceeded it under a two‑proton/ATP stoichiometry.
A technique is described, based on the distribution of rubidium, acetate and methylammonium ions, for the simultaneous estimation of membrane potential and pH gradient across the inner membrane of mitochondria. The technique requires less than 0.5 mg mitochondrial protein and is independent of many factors which interfere with electrode determinations of protonmotive force (Δ p ). With a limiting matrix volume of 0.4 μl/mg mitochondrial protein, the indicated value of Δ p for rat liver mitochondria is 228 mV in state 4, 170 mV in state 3, and –0.6 mV in the presence of rotenone and uncoupler. The relative contributions of the pH gradient and membrane potential are dependent on the availability of electrophoretically and electroneutrally translocatable species in the incubation medium. In a sucrose‐based medium containing 0.5 mM KCl, rotenone and uncoupler, the technique indicated a membrane potential of + 85 mV and a pH gradient of + 1.46 (acidic in the matrix compartment). In state 4, under no conditions examined did the pH gradient contribute more than 50% of the total protonmotive force. The hydrolysis of ATP generates an optimal Δ p of 220 mV. The proton conductance of the inner membrane is potential dependent, increasing when Δ p is greater than 200 mV. The extra‐mitochondrial phosphate potential sustainable by respiration was found to change in parallel to Δ p , but to exceed the latter parameter when based upon a stoichiometry of two protons translocated per ATP synthesised.
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