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1.
J Bioenerg Biomembr ; 49(5): 391-397, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28900787

ABSTRACT

According to the common view, weak acid uncouplers increase proton conductance of biological (and phospholipid bilayer) membranes, thus effecting H+ fluxes driven by their electrochemical gradients. Under certain conditions, however, uncouplers can induce unexpected effects opposite to the dissipation of H+ gradients. Results are presented here demonstrating CCCP-induced proton influx into Saccharomyces cerevisiae cytosol driven by the electrochemical potentials of CCCP and its CCCP- anions, independent of electrochemical H+-gradient. Another view of week acid uncouplers' action is proposed that is logically consistent with these observations.


Subject(s)
Membrane Potentials , Protons , Saccharomyces cerevisiae/metabolism , Uncoupling Agents/pharmacology , Biological Transport/drug effects , Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology , Hydrogen-Ion Concentration/drug effects , Membrane Potentials/drug effects
2.
Biochim Biophys Acta Biomembr ; 1859(10): 1974-1985, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28669766

ABSTRACT

Tok1p is a highly specific yeast plasma membrane potassium channel with strong outward directionality. Its opening is induced by membrane depolarization. Although the biophysical properties of Tok1p are well-described, its potentially important physiological role is currently largely unexplored. To address this issue, we examined the Tok1p activity following chemically-induced depolarization by measuring changes of plasma membrane potential (ΔΨ) using the diS-C3(3) fluorescence assay in a Tok1p-expressing and a Tok1p-deficient strain. We report that Tok1p channel activity in response to chemical stress does not depend solely on the extent of depolarization, as might have been expected, but may also be negatively influenced by accompanying effects of the used compound. The stressors may interact with the plasma membrane or the channel itself, or cause cytosolic acidification. All of these effects may negatively influence the Tok1p channel opening. While ODDC-induced depolarization exhibits the cleanest Tok1p activation, restoring an astonishing 75% of lost ΔΨ, higher BAC concentrations reduce Tok1p activity, probably because of direct interactions with the channel and/or its lipid microenvironment. This is not only the first study of the physiological role of Tok1p in ΔΨ maintenance under chemical stress, but also the first estimate of the extent of depolarization the channel is able to counterbalance.


Subject(s)
Fungal Proteins/metabolism , Membrane Potentials/physiology , Potassium Channels/metabolism , Stress, Physiological/physiology , Yeasts/metabolism , Cell Membrane
3.
J Bioenerg Biomembr ; 49(3): 273-279, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28405872

ABSTRACT

Yeast cells exhibit a negative surface potential due to negative charges at the cell membrane surface. Consequently, local concentrations of cations at the periplasmic membrane surface may be significantly increased compared to their bulk environment. However, in cell suspensions only bulk concentrations of cations can be measured directly. Here we present a novel method enabling the assessment of local pH at the periplasmic membrane surface which can be directly related to the underlying cell surface potential. In this proof of concept study using Saccharomyces cerevisiae cells with episomally expressed pH reporter, pHluorin, intracellular acidification induced by the addition of the protonophore carbonyl cyanide m-chlorophenylhydrazone (CCCP) was measured using synchronously scanned fluorescence spectroscopy (SSF). The analysis of titration curves revealed that the pH at the periplasmic surface of S. cerevisiae cells was about two units lower than the pH of bulk medium. This pH difference was significantly decreased by increasing the ionic strength of the bulk medium. The cell surface potential was estimated to amount to -130 mV. Comparable results were obtained also with another protonophore, pentachlorophenol (PCP).


Subject(s)
Hydrogen-Ion Concentration , Membrane Potentials , Periplasm/chemistry , Saccharomyces cerevisiae/chemistry , Carbonyl Cyanide m-Chlorophenyl Hydrazone , Green Fluorescent Proteins , Methods , Saccharomyces cerevisiae/cytology , Spectrometry, Fluorescence/methods
4.
Anal Chem ; 87(19): 9600-4, 2015 Oct 06.
Article in English | MEDLINE | ID: mdl-26325679

ABSTRACT

Since its introduction in 1998, genetically encoded pH-sensitive sensor ratiometric pHluorin proved to be a valuable tool for cell physiology studies. Here, we show how the sensitivity of pHluorin-based monitoring of intracellular pH changes performed with cell suspensions can be enhanced by using synchronously scanned fluorescence spectroscopy. In the suspensions of S. cerevisiae cells subjected to varying extracellular pH values, we have been able to measure statistically significant changes in intracellular pH of less than 0.1 unit, which were not detectable using a standard ratiometric approach.


Subject(s)
Green Fluorescent Proteins/chemistry , Saccharomyces cerevisiae/chemistry , Saccharomyces cerevisiae/cytology , Hydrogen-Ion Concentration , Saccharomyces cerevisiae/metabolism , Spectrometry, Fluorescence
5.
J Photochem Photobiol B ; 141: 139-44, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25463661

ABSTRACT

Here we present a fluorometric method for direct determination of supernatant-free fluorescence spectra generated from fluorescently stained cells in suspension. The key element in the new technique is the design of an adapter to a standard cuvette holder that makes it possible to measure front-face fluorescence spectra from thin layers of cells spun down to the bottom of a spectrofluorometric cuvette. We have demonstrated the applicability of this approach and its analytical potential using the suspensions of yeast cells stained with the potentiometric dye of 3,3'-dipropylthiadicarbocyanine, diS-C3(3), and with the specific cell-wall marker calcofluor.


Subject(s)
Spectrometry, Fluorescence , Carbocyanines/chemistry , Membrane Potentials , Saccharomyces cerevisiae/cytology , Spectrometry, Fluorescence/instrumentation
6.
J Fluoresc ; 24(2): 541-7, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24258003

ABSTRACT

Carbocyanine dye diS-C3(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval, F(580)/F(560) fluorescence emission ratio, wavelength of emission spectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C3(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). Here we show that data corresponding to the three latter spectral assessments of diS-C3(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments. On the other hand, experiments based on the effortless measurements of fluorescence intensities should be interpreted cautiously because controversial results can be obtained, depending on the particular choice of cell-to-dye concentration ratio and emission wavelength.


Subject(s)
Carbocyanines/chemistry , Membrane Potentials , Saccharomyces cerevisiae/chemistry , Spectrometry, Fluorescence/methods , Fluorescent Dyes/chemistry
7.
J Bioenerg Biomembr ; 45(6): 561-8, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24052423

ABSTRACT

Recently we introduced a fluorescent probe technique that makes possible to convert changes of equilibrium fluorescence spectra of 3,3'-dipropylthiadicarbocyanine, diS-C3(3), measured in yeast cell suspensions under defined conditions into underlying membrane potential differences, scaled in millivolts (Plasek et al. in J Bioenerg Biomembr 44: 559-569, 2012). The results presented in this paper disclose measurements of real early changes of plasma membrane potential induced by the increase of extracellular K(+), Na(+) and H(+) concentration in S. cerevisiae with and without added glucose as energy source. Whereas the wild type and the ∆tok1 mutant cells exhibited similar depolarization curves, mutant cells lacking the two Trk1,2 potassium transporters revealed a significantly decreased membrane depolarization by K(+), particularly at lower extracellular potassium concentration [K(+)]out. In the absence of external energy source plasma membrane depolarization by K(+) was almost linear. In the presence of glucose the depolarization curves exhibited an exponential character with increasing [K(+)]out. The plasma membrane depolarization by Na(+) was independent from the presence of Trk1,2 transporters. Contrary to K(+), Na(+) depolarized the plasma membrane stronger in the presence of glucose than in its absence. The pH induced depolarization exhibited a fairly linear relationship between the membrane potential and the pHo of cell suspensions, both in the wild type and the Δtrk1,2 mutant strains, when cells were energized by glucose. In the absence of glucose the depolarization curves showed a biphasic character with enhanced depolarization at lower pHo values.


Subject(s)
Hydrogen/metabolism , Potassium/metabolism , Saccharomyces cerevisiae/drug effects , Saccharomyces cerevisiae/metabolism , Sodium/metabolism , Cations, Monovalent/metabolism , Cell Membrane/metabolism , Fluorescent Dyes/chemistry , Fluorometry , Hydrogen-Ion Concentration , Membrane Potentials/drug effects
8.
FEMS Yeast Res ; 13(8): 782-95, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24028576

ABSTRACT

The effect of alcohols on cell membrane proteins has originally been assumed to be mediated by their primary action on membrane lipid matrix. Many studies carried out later on both animal and yeast cells have revealed that ethanol and other alcohols inhibit the functions of various membrane channels, receptors and solute transport proteins, and a direct interaction of alcohols with these membrane proteins has been proposed. Using our fluorescence diS-C3 (3) diagnostic assay for multidrug-resistance pump inhibitors in a set of isogenic yeast Pdr5p and Snq2p mutants, we found that n-alcohols (from ethanol to hexanol) variously affect the activity of both pumps. Beginning with propanol, these alcohols have an inhibitory effect that increases with increasing length of the alcohol acyl chain. While ethanol does not exert any inhibitory effect at any of the concentration used (up to 3%), hexanol exerts a strong inhibition at 0.1%. The alcohol-induced inhibition of MDR pumps was detected even in cells whose membrane functional and structural integrity were not compromised. This supports a notion that the inhibitory action does not necessarily involve only changes in the lipid matrix of the membrane but may entail a direct interaction of the alcohols with the pump proteins.


Subject(s)
ATP-Binding Cassette Transporters/antagonists & inhibitors , Alcohols/pharmacology , Saccharomyces cerevisiae Proteins/antagonists & inhibitors , Saccharomyces cerevisiae/drug effects , Saccharomyces cerevisiae/metabolism , ATP-Binding Cassette Transporters/genetics , ATP-Binding Cassette Transporters/metabolism , Adenosine Triphosphate/metabolism , Cell Membrane Permeability/drug effects , Drug Resistance, Fungal/genetics , Ions/metabolism , Microbial Sensitivity Tests , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/metabolism
9.
J Bioenerg Biomembr ; 44(5): 559-69, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22810564

ABSTRACT

The fluorescent dye 3,3'-dipropylthiadicarbocyanine, diS-C(3)(3), is a suitable probe to monitor real changes of plasma membrane potential in yeast cells which are too small for direct membrane potential measurements with microelectrodes. A method presented in this paper makes it possible to convert changes of equilibrium diS-C(3)(3) fluorescence spectra, measured in yeast cell suspensions under certain defined conditions, into underlying membrane potential differences, scaled in the units of millivolts. Spectral analysis of synchronously scanned diS-C(3)(3) fluorescence allows to assess the amount of dye accumulated in cells without otherwise necessary sample taking and following separation of cells from the medium. Moreover, membrane potential changes can be quantified without demanding calibration protocols. The applicability of this approach was demonstrated on the depolarization of Rhodotorula glutinis yeast cells upon acidification of cell suspensions and/or by increasing extracellular K(+) concentration.


Subject(s)
Carbocyanines/chemistry , Fluorescent Dyes/chemistry , Membrane Potentials/physiology , Rhodotorula/physiology , Rhodotorula/cytology
10.
J Fluoresc ; 22(4): 1183-8, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22538834

ABSTRACT

Fluorescence emission spectra of yeast cell suspensions stained with calcofluor have recently been identified as promising markers of variations in the quality of yeast cell wall. It is shown in this paper how the raw fluorescence spectra of calcofluor can be transformed to reliable spectral signatures of cell wall quality, which are independent of actual dye-to-cell concentrations of examined cell suspensions. Moreover, the presented approach makes it possible to assess basis fluorescence spectra that allows for the spectral unmixing of raw fluorescence spectra in terms of respective fluorescence contributions of calcofluor solvated in the suspension medium and bound to yeast cell walls.


Subject(s)
Benzenesulfonates/metabolism , Fluorescent Dyes/metabolism , Saccharomyces cerevisiae/cytology , Cell Wall/chemistry , Cell Wall/metabolism , Dose-Response Relationship, Drug , Glucose/pharmacology , Saccharomyces cerevisiae/chemistry , Saccharomyces cerevisiae/drug effects , Saccharomyces cerevisiae/metabolism , Spectrometry, Fluorescence , Staining and Labeling , Suspensions
11.
J Fluoresc ; 20(1): 343-52, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19882237

ABSTRACT

Fluorescence spectral properties of calcofluor (a popular stain used to visualize cell walls of bacteria, yeast and fungi) has been studied. The analysis of calcofluor fluorescence emission spectra measured in a wide range of solvents (including media containing chitin), and in yeast cell suspensions has revealed that the solvatochromic properties of calcofluor ensue essentially from the by solvent-solute hydrogen bonding, or from the hydrogen bonding to cell wall polysaccharides with an eventual contribution of calcofluor aggregation at the cell surface. Preliminary data suggest that calcofluor emission spectra can be employed as a practical marker of variations in the quality of yeast cell wall.


Subject(s)
Benzenesulfonates/chemistry , Benzenesulfonates/metabolism , Cell Wall/metabolism , Fluorescent Dyes/chemistry , Fluorescent Dyes/metabolism , Saccharomyces cerevisiae/cytology , Absorption , Chemical Phenomena , Chitin/metabolism , Hydrogen-Ion Concentration , Solutions , Spectrometry, Fluorescence , Staining and Labeling , Water/chemistry
12.
J Phys Chem B ; 111(14): 3640-50, 2007 Apr 12.
Article in English | MEDLINE | ID: mdl-17388522

ABSTRACT

We consider the properties of free pyrene probes inside gel- and fluidlike phospholipid membranes and unravel their influence on membrane properties. For this purpose, we employ atomic-scale molecular dynamics simulations at several temperatures for varying pyrene concentrations. Molecular dynamics simulations show that free pyrene molecules prefer to be located in the hydrophobic acyl chain region close to the glycerol group of lipid molecules. Their orientation is shown to depend on the phase of the membrane. In the fluid phase, pyrenes favor orientations where they are standing upright in parallel to the membrane normal, while, in the gel phase, the orientation is affected by the tilt of lipid acyl chains. Pyrenes are found to locally perturb membrane structure, while the nature of perturbations in the gel and fluid phases is completely different. In the gel phase, pyrenes break the local packing of lipids and decrease the ordering of lipid acyl chains around them, while, in the fluid phase, pyrenes increase the ordering of nearby acyl chains, thus having an opposite effect. Interestingly, this proposes a similarity to effects induced by cholesterol on structural membrane properties above and below the gel-fluid transition temperature. Further studies express a view that the orientational ordering of pyrene is not a particularly good measure of the acyl chain ordering of lipids. While pyrene ordering provides the correct qualitative behavior of acyl chain ordering in the fluid phase, its capability to predict the correct temperature dependence is limited.


Subject(s)
Computer Simulation , Fluorescent Dyes/chemistry , Membranes, Artificial , Pyrenes/chemistry , Gels/chemistry , Lipids/chemistry , Models, Chemical , Molecular Structure
13.
Biochemistry ; 43(26): 8303-11, 2004 Jul 06.
Article in English | MEDLINE | ID: mdl-15222743

ABSTRACT

Mutation of Arg(423) at the N-domain of Na(+)/K(+)-ATPase resulted in a large decrease of both TNP-ATP and ATP binding. Thus, this residue, localized outside the binding pocket, seems to play a key role in supporting the proper structure and shape of the binding site. In addition, mutation of Glu(472) also caused a large decrease of both TNP-ATP and ATP binding. On the basis of our computer model, we hypothesized that a hydrogen bond between Arg(423) and Glu(472) supports the connection of two opposite halves of the ATP-binding pocket. To verify this hypothesis, we have also prepared the construct containing both these mutations. Binding of neither TNP-ATP nor ATP to this double mutant differed from binding to any of the single mutants. This strongly supported the existence of the hydrogen bond between Arg(423) and Glu(472). Similarly, the conserved residue Pro(489) seems to be substantial for the proper interaction of the third and fourth beta-strands of the N-domain, which both contain residues that take part in ATP binding. Mutation of Asp(443) affected only ATP, but not TNP-ATP, binding, suggesting that these ligands adopt different positions in the nucleotide-binding pocket. On the basis of a recently published crystal structure [Håkansson, K. O. (2003) J. Mol. Biol. 332, 1175-1182], we improved our model and computed the interaction of these two ligands with the N-domain. This model is in good agreement with all previously reported spectroscopic data and revealed that Asp(443) forms a hydrogen bond with the NH(2) group of the adenosine moiety of ATP, but not TNP-ATP.


Subject(s)
Adenosine Triphosphate/analogs & derivatives , Adenosine Triphosphate/chemistry , Amino Acids/chemistry , Arginine/chemistry , Fluorescent Dyes/chemistry , Sodium-Potassium-Exchanging ATPase/chemistry , Adenosine/chemistry , Amino Acid Sequence , Animals , Aspartic Acid/chemistry , Binding Sites , Crystallography, X-Ray , Dose-Response Relationship, Drug , Electrophoresis, Polyacrylamide Gel , Genetic Vectors , Glutamic Acid/chemistry , Glutathione Transferase/metabolism , Hydrogen/chemistry , Hydrogen Bonding , Hydrolysis , Kinetics , Ligands , Magnetic Resonance Spectroscopy , Mice , Models, Molecular , Molecular Sequence Data , Mutation , Nucleotides/chemistry , Point Mutation , Proline/chemistry , Protein Binding , Protein Structure, Tertiary , Recombinant Fusion Proteins/chemistry , Sequence Homology, Amino Acid , Serine/chemistry , Software , Spectrophotometry , Temperature
14.
Biochemistry ; 42(21): 6446-52, 2003 Jun 03.
Article in English | MEDLINE | ID: mdl-12767226

ABSTRACT

Point mutations of a part of the H(4)-H(5) loop (Leu(354)-Ile(604)) of Na(+)/K(+)-ATPase have been used to study the ATP and TNP-ATP binding affinities. Besides the previously reported amino acid residues Lys(480), Lys(501), Gly(502), and Cys(549), we have found four more amino acid residues, viz., Glu(446), Phe(475), Gln(482), and Phe(548), completing the ATP-binding pocket of Na(+)/K(+)-ATPase. Moreover, mutation of Arg(423) has also resulted in a large decrease in the extent of ATP binding. This residue, localized outside the binding pocket, seems to play a key role in supporting the proper structure and shape of the binding site, probably due to formation of a hydrogen bond with Glu(472). On the other hand, only some minor effects were caused by mutations of Ile(417), Asn(422), Ser(445), and Glu(505).


Subject(s)
Adenosine Triphosphate/metabolism , Amino Acids/chemistry , Sodium-Potassium-Exchanging ATPase/chemistry , Animals , Binding Sites , Brain/enzymology , Cysteine/chemistry , Dose-Response Relationship, Drug , Genetic Complementation Test , Genetic Vectors , Glutamic Acid/chemistry , Glutamine/chemistry , Hydrogen Bonding , Mice , Models, Molecular , Mutagenesis, Site-Directed , Phenylalanine/chemistry , Point Mutation , Protein Binding , Protein Structure, Secondary , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/metabolism , Recombinant Proteins/chemistry , Spectrophotometry, Infrared , Spectroscopy, Fourier Transform Infrared
15.
Biochem Biophys Res Commun ; 297(1): 154-9, 2002 Sep 13.
Article in English | MEDLINE | ID: mdl-12220524

ABSTRACT

The ATP-binding site of Na(+)/K(+)-ATPase is localized on the large cytoplasmic loop of the alpha-subunit between transmembrane helices H(4) and H(5). Site-directed mutagenesis was performed to identify residues involved in ATP binding. On the basis of our recently developed model of this loop, Ser(445), Glu(446), and Phe(475) were proposed to be close to the binding pocket. Replacement of Phe(475) with Trp and Glu(446) with Gln profoundly reduced the binding of ATP, whereas the substitution of Ser(445) with Ala did not affect ATP binding. Fluorescence measurements of the fluorescent analog TNP-ATP, however, indicated that Ser(445) is close to the binding site, although it does not participate in binding.


Subject(s)
Adenosine Triphosphate/analogs & derivatives , Adenosine Triphosphate/metabolism , Sodium-Potassium-Exchanging ATPase/metabolism , Animals , Binding Sites , Fluorescent Dyes/metabolism , Glutamic Acid/metabolism , Mice , Models, Molecular , Phenylalanine/metabolism , Protein Conformation , Protein Subunits , Recombinant Fusion Proteins/metabolism , Serine/metabolism
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