[Detection and functional role of local gradients of H+-ions on the intracellular mitochondrial membrane with covalently linked pH-probe]. / Obnaruzhenie i funktsional'naia rol' lokal'nykh gradientov H+-ionov na vnutrennei membrane mitokhondrii s kovalentno prisoedinennym H-zondom.

The study is devoted to the registration of local H+ gradients on the inner membrane of mitochondria under conditions of H+ pump functioning were recorded. By using a covalently linked pH probe (fluorescein isothiocyanate), a local increase in the activity of hydrogen ions on the outer face of the inner mitochondrial membrane in the presence of the respiration substrate at increased permeability of the membrane for K+ was registered. It was also found that the buffer capacity of medium affects the respiration rate of completely uncoupled mitochondria; a change in respiration rate strictly correlates with changes in local H+ gradients on the mitochondrial membrane. It was concluded that local gradients of H+ activity can control the rate of functioning of H+ pumps. It was shown that, under certain conditions, the system of H+ pumps incorporated into succinate oxidase of mitochondria functions as a nonliner system.

[Two qualitatively different structuro-functional states of mitochondria]. / Dva kachestvenno razlichnykh strukturno-funktsional'nykh sostoiania mitokhondrii.

Low (120 mosM) tonicity of incubation media of mitochondria was found to be associated with anomalous phase transition at 19--26 degrees C. A rise in temperature caused a decrease in the pyrene excitation in border lipids of the mitochondrial membrane. Within this temperature range the quenching of intrinsic protein fluorescence by pyrene was sharply decreased. It may be inferred from these data that at 100mosM tonicity and temperatures below 19 degrees C, mitochondrial membrane proteins are in an aggregated state. At temperatures above phase transition protein deaggregation takes place. It was shown that a decrease in tonicity from 300 to 120 mosM at 15 degrees C or a rise in temperature from 15 degrees to 37 degrees C at 300 mosM tonicity increased the phosphorylation of the 52 kDa mitochondrial protein. It was assumed that swelling of mitochondria in hypotonic media simulates one of the steps of the hormone-induced signal transfer in mitochondria in vivo.

[Structural and kinetic parameters of the oxidative phosphorylation system, participating in the synchronization of mitochondrial respiratory chain and ATP-synthetase functions]. / Poisk strukturnykh i kineticheskikh parametrov sistemy okislitel'nogo fosforilirovaniia, uchastvuiushchikh v sinkhronizatsii raboty dykhatel'noi tsepi i ATP-sintetazy mitokhondrii.

The structural and kinetic parameters of the oxidative phosphorylation system responsible for synchronization of the respiratory chain and ATP-synthetase function in mitochondria were studied. It was shown that regulation of ATP-synthetase function by the respiratory chain can be realized only within the whole ATP-synthetase complex (F0F1). NADH dehydrogenase and succinate dehydrogenase doe not control synchronization of ATP-synthetase function in the mitochondria. Data from the inhibitory analysis suggest that the ATP-synthetase function depends on the rate of the enzyme operation but not on the redox state of the respiratory chain carriers.

[Synchronization of the function of respiratory chain enzymes and ATP-synthetase in energized mitochondria]. / Sinkhronizatsiia raboty fermentov dykhatel'noi sepi i ATP-sintetazy énergizovannykh mitokhondrii.

The present study revealed that the previously described effect of ATP-synthetase inhibition concomitant with inhibition of the respiratory chain functioning could be observed under different absolute values of delta phi on the mitochondrial membrane. This points out that the membrane potential is not a unique regulator in the coupling of the ATP-synthetase and respiratory chain activities. At the same time, we succeeded in obtaining some evidence testifying that under conditions of ATP-synthetase inhibition the amount of functioning respiratory chains has to be proportional the functioning of the ATP-synthetases units. The osmolarity of the incubation medium was shown to control the state of the oxidative phosphorylation system. The respiratory chain and ATP-synthetase should be considered as an enzymatic supercomplex only when the osmolarity is close to 150-300 mOsm (within the physiological range). The coupling effectivity (ADP/O) of mitochondria under these conditions is maximal. It is concluded that the respiratory chain and ATP-synthetase are tightly bound from the kinetic point of view. The ATP-synthetase inhibition induces proportional inhibition of the respiratory chain enzymes and vice versa, the respiratory chain inhibition induces proportional inhibition of ATP-synthetase.

[Mechanism of the Crabtree effect: influence of pH on the rate of mitochondrial respiration]. / O mekhanizme éffekta krebtri: vliianie pH sredy inkubatsii na skorost' dykhaniia mitokhondrii.

A detailed study of dependence of mitochondrial respiration on pH of incubation medium has been carried out. It was shown that during oxidation of malic, succinic and ascorbic acids mitochondrial respiration shows a sharp fall, when the pH of incubation medium is decreased from 7.5 to 6.5. It was assumed that one of the possible causes of the Crabtree effect is a reduction of the pH value of the cytoplasm.

[Control of proton transport across the double electrical layers of mitochondrial membranes]. / Reguliatsiia parenosa protona cherez dvoinoi élektricheskii sloi na membrane mitokhondrii.

The effects of cardiolipin, dodecylsulfate anion and K+ on inhibition of respiration of intact and briefly frozen mitochondria by electrophylic compounds, e. g. beta-haloidalkylamines-p-(N,N-di-2-chlorethylamino)phenylacetic (I) and--phenylbutyric (II) acids were studied. It was shown that in K+-containing media the increase of the negative surface charge of the frozen mitochondrial membrane enhances the inhibition of mitochondrial respiration. In media without K+ this affect is absent. The inhibition of mitochondrial respiration by I and II is due to local increase of activity of the acids in mitochondrial membrane in the course of hydrolysis. It was assumed that the double electrical layers hamper the transport of the acid from the hydrophobic zone of the membrane into the environment including the water phase. Using this model, it was demonstrated that when the double electrical layer is destroyed, the inhibition of respiration by I is decreased at increased buffer capacity of the incubation medium. Correspondingly, in intact mitochondria the buffer capacity of the medium does not practically affect the inhibition of respiration by I.

[Regulation of the reaction rate of ATP synthesis in intact mitochondria]. / Reguliatsiia skorosti reaktsii sinteza ATF v intaktnykh mitokhondriiakh.

High concentrations of respiration inhibitors are known to sharply decrease the membrane potential in mitochondria. The effect of relatively low concentrations of oxidative phosphorylation inhibitors on the value of membrane potential of intact mitochondria and on the rate of respiration and phosphorylation as well was studied. It has been found that within a certain concentration range the inhibitors of oxidative phsophorylation--malonic acid, sodium cyanide m-chlorophenyl hydrozonecarbonylcyanide, sharply decrease the phosphorylation rate (by 70 divided by 90%) but do not practically a affect the membrane potential value of intact mitochondria in the state 3 according to Chance.

[Effect of luliberin on the activities of mitochondrial respiratory enzymes]. / Vliianie liuliberina na aktivnost' mitokhondrial'nykh dykhatel'nykh fermentov.

Luliberin, a luteinizing hormone-releasing hormone, was shown to inhibit the respiratory enzymes of rat liver mitochondria and submitochondrial particles prepared from beef heart mitochondria. At the hormone concentration of 8.10(-6) M the NADH-oxidase activity of the submitochondrial particles was inhibited by 50%. The fragments of the hormone and its analogs and pyroglutamic acid, oxytocin and bradikinin possessed practically no inhibiting effects. In the case of submitochondrial particles the inhibition was only observed in the presence of Ca2+ and was significantly decreased after addition of bovine serum albumin and phospholipase inhibitors -- butacaine and dicaine. It is assumed that the effect of luliberin on the respiratory chain is mediated through mitochondrial phospholipase.

[Inhibitors of the slow stage of proton transfer in the link connecting respiration with mitochondrial phosphorylation]. / Ingibitory medlennoi stadii perenosa protona v zvene soprazheniia dykhaniia i fosforilirovaniia mitokhondrii

Electrophilic agents--derivatives of carbonic acids--are found to inhibit respiration, ATP synthesis and reverse electrone transport in intact mitochondria. The inhibition of respiration and ATPase was observed in intact mitochondria at 3 and 3u states (by Chance). Inhibitors concentrations, which caused 50% inhibition, were approximately the same. Sharp decrease of the effect of electrophilic inhibitors on respiration and ATPase activity in mitochondria and submitochondrial particles with substantially impaired coupling system was observed. The following conclusions are drawn on the basis of the data obtained: 1) electrophilic inhibitor attack the coupling site of respiration and ATP synthesis in mitochondria; 2) the reaction of the proton transport from the respiration proton pump to ATP synthetase is one of the slowest steps of the process of ATP-synthesis in mitochondria. A scheme of working the coupling system is suggested which includes the step of proton lateral diffusion.