Role Of Membrane Potential Research Articles

Role of membrane potential in protein folding and domain formation during secretion in escherichia coli

The synthesis and processing of the periplasmic components of the leucine transport system of E coli have been studied to determine the role played by transmembrane potential in protein secretion. Both the leucine-isoleucine-valine binding protein and the leucine-specific binding protein are synthesized as precursors with 23 amino acid N-terminal leader sequences. The processing of these precursors is sensitive to the transmembrane potential. Since the amino acid sequence and the crystal structure have been determined for the leucine-isoleucine-valine binding protein, it and the closely related leucine-specific binding protein represent convenient models in which to examine the mechanism of protein secretion in E coli. A model for secretion has been proposed, suggesting a role for transmembrane potential. In this model, the N-terminal amino acid sequence of the precursor is assumed to form a hairpin of two helices. The membrane potential may orient this structure to make it accessible to processing. In addition, the model suggests that a negatively charged, folded domain of the secretory protein may electrophorese toward the trans-positive side of the membrane, thus providing an additional role for the transmembrane potential.

Regulation of Ca2+ efflux in rat liver mitochondria. Role of membrane potential.

The paper analyzes the relationship between membrane potential (delta psi), steady state pCao (-log [Ca2+] in the outer aqueous phase) and rate of ruthenium-red-induced Ca2+ efflux in liver mitochondria. Energized liver mitochondria maintain a pCao of about 6.0 in the presence of 1.5 mM Mg2+ and 0.5 mM Pi. A slight depression of delta psi results in net Ca2+ uptake leading to an increased steady state pCao. On the other hand, a more marked depression of delta psi results in net Ca2+ efflux, leading to a decreased steady-state pCao. These results reflect a biphasic relationship between delta psi and pCao, in that pCao increases with the increase of delta psi up to a value of about 130 mV, whereas a further increase of delta psi above 130 mV results in a decrease of pCao. The phenomenon of Ca2+ uptake following a depression of delta psi is independent of the tool used to affect delta psi whether by inward K+ current via valinomycin, or by inward H+ current through protonophores or through F1-ATP synthase, or by restriction of e- flow. The pathway for Ca2+ efflux is considerably activated by stretching of the inner membrane in hypotonic media. This activation is accompanied by a decreased pCao at steady state and by an increased rate of ruthenium-red-induced Ca2+ efflux. By restricting the rate of e- flow in hypotonically treated mitochondria, a marked dependence of the rate of ruthenium-red-induced Ca2+ efflux on the value of delta psi is observed, in that the rate of Ca2+ efflux increases with the value of delta psi. The pCao is linearly related to the rate of Ca2+ efflux. Activation of oxidative phosphorylation via addition of hexokinase + glucose to ATP-supplemented mitochondria, is followed by a phase of Ca2+ uptake, which is reversed by atractyloside. These findings support the view that Ca2+ efflux in steady state mitochondria occurs through an independent, delta psi-controlled pathway and that changes of delta psi during oxidative phosphorylation can effectively modulate mitochondrial Ca2+ distribution by inhibiting or activating the delta psi-controlled Ca2+ efflux pathway.

Role of membrane potential in the response of rat small mesenteric arteries to exogenous noradrenaline stimulation.

1. We have made simultaneous measurements of membrane potential and wall tension in rat 200 microns mesenteric arteries. 2. The resting membrane potential was -59.2 +/- 0.4 mV and stable (218 measurements, fifty-two vessels). 3. With maximal exogenous noradrenaline stimulation (10 microM) the membrane depolarized to about -34 mV. During the onset of tension development oscillations (period about 6 sec) in both tension and membrane potential were often seen; the membrane potential changes led the tension changes by about 1.2 sec. 4. In the presence of increased K+ (e.g. 40 mM), vessels had an increased noradrenaline sensitivity, and here noradrenaline stimulation produced little change in membrane potential. 5. With maximal K+ stimulation (85 mM), in the presence of phentolamine (1 microM), the membrane depolarized to about -17 mV, the tension being about 70% of the maximal noradrenaline response. 6. In the presence of phentolamine (1 microM), noradrenaline caused hyperpolarization without tension development. The hyperpolarization was inhibited by propranolol and mimicked by isoprenaline. 7. The results suggest that in these small vessels membrane potential variations are not essential to, but have an important modulating influence on, the tension response to exogenous noradrenaline.

Role of membrane potential and calcium in chemotactic sensing by bacteria

Changes in Escherichia coli membrane potential in response to a wide variety of chemotactic stimuli were measured using a permeant, lipophilic cation (tetraphenylphosphonium chloride) and a fluorescent dye (3-propyl-2-(5-(3-propyl-2(3H)-benzothiazolylidene)-1,3-pentadienyl)iodide). Some attractants and repellants caused permanent, monotonic depolarizations or hyperpolarizations. Not all chemoeffectors, however, produced potential changes, and the direction of change did not correlate with physiological responses to these compounds. Moreover, changes were observed in a number of chemotactic mutants. From these results, we conclude that perturbations in membrane potential effected by chemical stimuli are not related to chemotactic sensing. These findings, and the close correlation between cytoplasmic ionic conditions and membrane potential, led us to examine the role of calcium in chemotaxis. By growing cells in the presence of a calcium chelator, we were able to lower cellular calcium levels over tenfold, with no change in behavior. These results indicate that sensory transduction in these cells is not mediated by this cation.

Role of membrane potential and ATP in complex formation between Escherichia coli male cells and filamentous phage fd.

Mutant strains of Escherichia coli male cells defective in Ca2+,Mg2+-dependent ATPase (unc) were constructed and tested for their ability to form a complex between sex pili and the filamentous phage fd under conditions where either the membrane potential or the cellular concentration of ATP was lowered. The uncoupler carbonyl cyanide m-chlorophenylhydrazone and the respiratory inhibitor cyanide, as well as valinomycin-K+ and colicin E1, all markedly diminished complex formation, indicating that the maintenance of a membrane potential, but probably not the pH gradient, is essential for the formation of the complex. Since complex formation with freshly centrifuged cells (which initially lacked sex pili) as well as with preincubated cells (in which pre-existing pili were available for complex formation) was inhibited by exposure to the inhibitors, energy seems to be required for both the reappearance (probably assembly) and the maintenance of sex pili on the cell surface. Brief exposure of freshly centrifuged cells to arsenate resulted in only partial inhibition of complex formation. However, marked inhibition of complex formation was observed following exposure to arsenate of preincubated cells possessing sex pili. This indicates that compounds such as ATP may also be required for maintenance of sex pili on the cell surface.

The role of membrane potential in determining rates of lateral diffusion in the plasma membrane of mammalian cells.

The role of membrane potential in determining rates of lateral diffusion in the plasma membrane of mammalian cells.

The role of membrane potential in the tight binding of adenine nucleotides of chloroplast CF 1

The role of membrane potential in the tight binding of adenine nucleotides of chloroplast CF 1