valinomycin and methylamine

The fluorescent compound Hoechst 33342 is a substrate for many multidrug resistance (MDR) transporters and is widely used to characterize their transport activity. We have constructed mutants of the adenosine triphosphate (ATP) binding cassette (ABC)-type MDR transporter LmrA of Lactococcus lactis that are defective in ATP hydrolysis. These mutants and wild-type LmrA exhibited an atypical behavior in the Hoechst 33342 transport assay. In membrane vesicles, Hoechst 33342 transport was shown to be independent of the ATPase activity of LmrA, and it was not inhibited by orthovanadate but sensitive to uncouplers that collapse the proton gradient and to N,N'-dicyclohexylcarbodiimide, an inhibitor of the F0F1-ATPase. In contrast, transport of Hoechst 33342 by the homologous, heterodimeric MDR transporter LmrCD showed a normal ATP dependence and was insensitive to uncouplers of the proton gradient. With intact cells, expression of LmrA resulted in an increased rate of Hoechst 33342 influx while LmrCD caused a decrease in the rate of Hoechst 33342 influx. Cellular toxicity assays using a triple knockout strain, i.e., L. lactis delta lmrA delta lmrCD, demonstrate that expression of LmrCD protects cells against the growth inhibitory effects of Hoechst 33342, while in the presence of LmrA, cells are more susceptible to Hoechst 33342. Our data demonstrate that the LmrA-mediated Hoechst 33342 transport in membrane vesicles is influenced by the transmembrane pH gradient due to a pH-dependent partitioning of Hoechst 33342 into the membrane.

Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Amino Acid Substitution; ATP-Binding Cassette Transporters; Bacterial Proteins; Benzimidazoles; Biological Transport; Cell Proliferation; Dicyclohexylcarbodiimide; Fluorescent Dyes; Hydrogen-Ion Concentration; Ionophores; Lactococcus lactis; Liposomes; Membrane Transport Proteins; Methylamines; Multidrug Resistance-Associated Proteins; Mutagenesis, Site-Directed; Nigericin; Proton-Motive Force; Proton-Translocating ATPases; Recombinant Proteins; Spectrometry, Fluorescence; Valinomycin; Vanadates

Conditions for the use of both [14C]methylamine and 5, 5-dimethyl[14C]oxa-azolidine-2,4-dione (DMO) to measure the H+ concentration of intracellular compartments of monomorphic long thin bloodstream forms of Trypanosoma brucei were established. Neither probe was actively transported or bound to internal components of the cell and both probes equilibrated passively with a t1/2 close to 8 min. DMO was excluded from cells, while methylamine was accumulated but not metabolized. Solution of the three-compartment problem revealed that, when cells were respiring aerobically on glucose at an external pH of 7.5, the cytoplasmic pH was in the range 6.99-7.03, the pH of the mitochondrial matrix was 7.71-7.73, and the algebraic average pH of the various endosomal compartments was 5.19-5.50. Similar values were found when cells were respiring aerobically on glycerol. However, bloodstream forms of T. brucei could not maintain a constant internal H+ concentration outside the external pH range 7.0-7.5, and no evidence for the presence of an H+/Na+ exchanger was found. Full motility and levels of pyruvate production were maintained as the external pH was raised as high as 9.5, suggesting that these cells tolerate significant internal alkalinisation. However, both motility and pyruvate production were severely inhibited under acidic conditions, and the cells deteriorated rapidly below an external pH of 6.5. Physiologically, the plasma membrane of T. brucei had low permeability to H+ and the internal pH was unaffected by changes in Deltapsip, which is dominated by the potassium diffusion potential. However, in the presence of FCCP, the internal pH fell rapidly about 0.5 pH unit and came into equilibrium with Deltapsip. Oligomycin abolished the mitochondrial pH gradient (DeltapHm) selectively, whereas chloroquine abolished only the endosomal pH gradient (DeltapHe). The pH gradient across the plasma membrane (DeltapHp) alone could be abolished by careful osmotic swelling of cells. The plasma membrane had an inwardly directed proton-motive force (DeltaPp) of -52 mV and an inwardly directed sodium-motive force (DeltaNp) of -149 mV, whereas the mitochondrial inner membrane had only an inwardly directed DeltaPm of -195 mV. The pH gradient across the endosomal membranes was not accompanied by an electrical gradient. Consequently, endosomal membranes had an algebraically average outwardly directed DeltaPl within the range + 89 to +110 mV, depending on the measurement method.

Topics: Animals; Antimalarials; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Cell Membrane; Chloroquine; Dimethadione; Dose-Response Relationship, Drug; Endosomes; Glycerol; Hydrogen-Ion Concentration; Ionophores; Kinetics; Membrane Potentials; Methylamines; Mitochondria; Monensin; Nystatin; Oligomycins; Potassium Chloride; Proton-Motive Force; Protons; Pyruvates; Sodium; Time Factors; Trypanosoma brucei brucei; Uncoupling Agents; Valinomycin; Water

We aimed to ascertain whether pyrethroid insecticides could influence the vesicular transport of the excitatory amino acid glutamate. The incubation of rat cortical synaptic vesicles with resmethrin and permethrin, consistently stimulated both ATP-dependent and -independent uptake of [3H]glutamate, while not evoking depletion of its vesicular content. Both processes were counteracted by valinomycin, a dissipator of the transmembrane potential gradient (deltapsi(sv)). Meanwhile, the vesicular influx of 36Cl- anions was impaired by pyrethroid concentrations which did not affect the ATP-dependent uptake of [14C]methylamine, as a marker for the proton gradient (deltapH). Thus, the stimulation of glutamate transport appeared to involve mainly the deltapsi(sv). A self-attenuating effect of selected pyrethroids on putatively enhanced excitatory transmission in severe intoxication is suggested.

Topics: Adenosine Triphosphate; Animals; Biological Transport; Carbon Radioisotopes; Chlorides; Glutamic Acid; Insecticides; Ionophores; Male; Methylamines; Permethrin; Pyrethrins; Rats; Rats, Sprague-Dawley; Synaptic Vesicles; Tritium; Valinomycin

The uptake of mefloquine and chloroquine by Plasmodium chabaudi-infected mouse erythrocytes was measured in the presence and absence of ionophores and uncoupler in order to distinguish between the pH-dependent and pH-independent absorption of these drugs. Nigericin and CCCP (carbonylcyanide m-chlorophenylhydrazone) were used to relax the proton gradients and electrical potentials across the membranes. It was found that 40-60% of the mefloquine uptake, and 90% of the chloroquine uptake, was pH-dependent, the remainder being due to passive binding to cellular constituents. The distribution ratio of the pH-dependent uptake for mefloquine was about three times greater than for chloroquine. According to the lysosomotropic weak base hypothesis in which the neutral forms of weak bases are assumed to equilibrate across membranes, the mefloquine distribution should be smaller than the chloroquine distribution: since mefloquine is singly charged and chloroquine is doubly charged, the chloroquine distribution ratio should vary as the square of the mefloquine ratio. We interpret the greater uptake ratio of mefloquine to be evidence for the involvement of secondary active transport, with drug uptake being coupled to proton outflow by an antiporter protein. It is proposed that the uptake of mefloquine is electrogenic, with the proton gradient and the electrical potential both contributing to the driving force, but that the proton gradient alone is responsible for the chloroquine uptake.

Topics: Animals; Antimalarials; Biological Transport; Carbonyl Cyanide m-Chlorophenyl Hydrazone; Chloroquine; Dose-Response Relationship, Drug; Electrochemistry; Erythrocyte Membrane; Hydrogen-Ion Concentration; Ionophores; Mefloquine; Methylamines; Mice; Plasmodium; Quinolines; Temperature; Valinomycin

The transmembrane pH gradient maintained by nonrespiring, uncoupled heart mitochondria has been estimated using the distribution of methylamine and of 5,5-dimethyl-2,4-oxazolidinedione (DMO) and compared with the delta pH reported by the fluorescent probe 2,7-biscarboxyethyl-5(6)-carboxyfluorescein (BCECF). Under these conditions the protonmotive force approaches zero and the membrane potential (delta psi) should equal 59 delta pH (P. Mitchell and J. Moyle (1969) Eur. J. Biochem. 7, 471-484). The delta pH reported by DMO corresponds closely to that estimated by BCECF and is consistent with a Donnan potential of no greater than about -30 mV (interior negative) for nonenergized mitochondria in a sucrose medium. This potential appears to result from the presence of immobile negative charges in the matrix and is eliminated by addition of 10 to 25 mM KCl. Measurements of delta pH using the methylamine and of delta tsi using the distribution of 42K+ in the presence of valinomycin result in an apparent overestimation of these parameters due to binding of these components to negative sites on the membrane. Increasing ionic strength decreases this contribution of surface potential, but significant binding can still be detected in 100 mM KCl. These studies suggest that 42K+ (or 86Rb+) is far from an ideal probe for measuring delta tsi in respiring mitochondria and may significantly overestimate this parameter, especially in sucrose media.

Topics: Animals; Cattle; Diffusion; Dimethadione; Fluoresceins; Hydrogen-Ion Concentration; Membrane Potentials; Methylamines; Mitochondria, Heart; Osmolar Concentration; Oxazoles; Oxygen Consumption; Potassium; Rubidium; Valinomycin

The uptake of dibucaine into large unilamellar vesicles in response to proton gradients (delta pH; inside acidic) or membrane potentials (delta psi; inside negative) has been investigated. Dibucaine uptake in response to delta pH proceeds rapidly in a manner consistent with permeation of the neutral (deprotonated) form of the drug, reaching a Henderson-Hasselbach equilibrium where [dibucaine]in/[dibucaine]out = [H+]in/[H+]out and where the absolute amount of drug accumulated is sensitive to the buffering capacity of the interior environment. Under appropriate conditions, high absolute interior concentrations of the drug can be achieved (approximately 120 mM) in combination with high trapping efficiencies (in excess of 90%). Dibucaine uptake in response to delta psi proceeds more than an order of magnitude more slowly and cannot be directly attributed to uptake in response to the delta pH induced by delta psi. This induced delta pH is too small (less than or equal to 1.5 pH units) to account for the transmembrane dibucaine concentration gradients achieved and does not come to electrochemical equilibrium with delta psi. Results supporting the possibility that the charged (protonated) form of dibucaine can be accumulated in response to delta psi were obtained by employing a permanently positively charged dibucaine analogue (N-methyldibucaine). Further, the results suggest that delta psi-dependent uptake may depend on formation of a precipitate of the drug in the vesicle interior. The uptake of dibucaine into vesicles in response to ion gradients is of direct utility in drug delivery and controlled release applications and is related to processes of drug sequestration by cells and organelles in vivo.

Topics: 1,2-Dipalmitoylphosphatidylcholine; Carbon Radioisotopes; Dibucaine; Hydrogen-Ion Concentration; Inulin; Kinetics; Lipid Bilayers; Magnetic Resonance Spectroscopy; Membrane Potentials; Methylamines; Models, Biological; Potassium; Valinomycin

Isolated beef heart mitochondria were treated with A23187 in the presence of different concentrations of Mg2+ or EDTA to establish varying levels of total mitochondrial Mg2+. The Mg2+ content was related to the rate of passive swelling of the mitochondria in potassium acetate and other potassium salts in which swelling is presumed to depend on K+ entry via an endogenous K+/H+ antiport. Swelling in these salts does not commence until Mg2+ has been depleted from an initial value of 36 nmol X mg-1 of protein to 8 nmol/mg-1, or less. Below this level, swelling increases linearly with decreasing Mg2+ to a maximum rate at 2 nmol of Mg2+ X mg-1. Rotenone-treated heart mitochondria suspended in 75 mM potassium acetate at pH 7.80 show no delta pH by 5,5-dimethyl-2,4-oxazolidinedione distribution. Distribution of methylamine also shows essentially no delta pH under these conditions when allowance is made for binding of [14C]methylamine by mitochondrial membranes under these conditions. Addition of A23187 results in a small and transient delta pH (delta pH less than 0.14, acid interior) as measured by methylamine distribution. Estimation of the maximum matrix free Mg2+ concentration from the maximum delta pH observed and the external free Mg2+ concentration at equilibrium with A23187 shows that swelling is not initiated until matrix free Mg2+ is decreased to below 150 microM. An independent estimate of free Mg2+ using a null-point procedure gives a lower, but quite similar value (50 microM) for maximum matrix free Mg2+ when swelling commences. The large depletion of total and free Mg2+ that is required to activate swelling in potassium acetate (and presumably K+/H+ antiport activity) does not appear to be compatible with previous indications that free Mg2+ acts as a "carrier brake" to regulate K+ extrusion from the mitochondrion on such an antiport (Garlid, K. D. (1980) J. Biol. Chem. 255, 11273-11279). The removal of a tightly bound component of mitochondrial Mg2+ is closely related to increased K+ permeability and increased passive swelling in potassium salts. This Mg2+ appears to play a role in the maintenance of mitochondrial membrane structure and integrity.

Topics: Animals; Calcimycin; Carbonyl Cyanide m-Chlorophenyl Hydrazone; Carrier Proteins; Cattle; Edetic Acid; Magnesium; Mathematics; Methylamines; Mitochondria, Heart; Permeability; Potassium; Potassium-Hydrogen Antiporters; Valinomycin

Apical plasma membrane vesicles isolated from bovine tracheal epithelium were found to possess both an electrical potential gradient (delta psi) and a transmembrane pH gradient (delta pH). The delta psi was calculated from the distribution of 86Rb+ in the presence of the ionophore valinomycin, and delta pH was determined from the distribution of [14C]methylamine under conditions of apparent equilibrium. Maximal values for delta psi of -54.3 +/- 2.5 mV and for delta pH of 0.75 +/- 0.07 pH units were obtained under low ionic strength conditions. Increasing the ionic strength by the addition of 50 mM of either permeant or impermeant electrolytes reduced delta psi to near zero values. The delta pH varied in parallel with the delta psi. The results suggest that both 86Rb+ in the presence of valinomycin and H+ are in a Donnan equilibrium with impermeant negative charge in the vesicle interior.

Topics: Animals; Cattle; Cell Membrane Permeability; Hydrogen-Ion Concentration; In Vitro Techniques; Membrane Potentials; Membranes; Methylamines; Rubidium; Trachea; Valinomycin

Clathrin-coated vesicles isolated from calf brain contain an ATP-dependent proton pump. Proton movement was monitored by measuring [14C]methylamine distribution. Addition of Mg2+ and ATP to coated vesicles equilibrated with [14C]methylamine resulted in the generation of a 4- to 5-fold concentration gradient, corresponding to a delta pH of 0.6-0.7 units between the medium and the acidic inside of the coated vesicles. ATP-dependent [14C]methylamine uptake was abolished by the proton ionophore carbonylcyanide p-trifluoromethoxyphenylhydrazone (FCCP) and partially inhibited by the carboxyl reagent N,N'-dicyclohexylcarbodiimide but was unaffected by the Na+, K+-ATPase inhibitors strophanthidin (100 microM) and vanadate (10 microM) and the mitochondrial ATPase inhibitors oligomycin (10 microgram/ml) and aurovertin (1 microgram/ml). GTP, but not the nonhydrolyzable analog 5'-adenylyl imidodiphosphate, could support [14C]methylamine uptake. Dissipation of the membrane potential with K+ and valinomycin resulted in stimulation of [14C]methylamine uptake, whereas both FCCP and valinomycin stimulated the strophanthidin-resistant ATPase activity. These results are consistent with the existence of an electrogenic, ATP-dependent proton pump in clathrin-coated vesicles. This proton pump may play a role in the acidification events that are essential in receptor-mediated endocytosis.

Topics: Adenosine Triphosphatases; Animals; Brain; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Cattle; Clathrin; Coated Pits, Cell-Membrane; Endosomes; Magnesium; Membrane Potentials; Membrane Proteins; Methylamines; Potassium; Proton-Translocating ATPases; Valinomycin

To ascertain the function of H+ flux in active Ca2+ transport into sarcoplasmic reticulum vesicles, the effect of pH gradient on Ca2+ transport was examined. A transient H+ gradient (inside-acidic) was imposed on K+-loaded sarcoplasmic reticulum vesicles with the aid of K+-H+ exchange driven by nigericin. This proton gradient was dissipated rapidly and concomitantly with ATP-driven Ca2+ transport. Under these conditions, the initial rate of the Ca2+ uptake was increased about 1.5-fold. The stimulation of Ca2+ uptake was completely lost when the pH gradient was cancelled with an uncoupler plus membrane permeable cation before Ca2+ uptake. These results are interpreted in terms of H+ efflux coupled with Ca2+ transport.

Topics: Animals; Biological Transport, Active; Calcium; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Hydrogen; Hydrogen-Ion Concentration; Methylamines; Nigericin; Potassium; Protons; Rabbits; Sarcoplasmic Reticulum; Valinomycin