Resonance electroconformational coupling: A proposed mechanism for energy and signal transductions by membrane proteins

1989 ◽  
Vol 9 (1) ◽  
pp. 13-26 ◽  
Author(s):  
Tian Yow Tsong ◽  
Dao-Sheng Liu ◽  
Francoise Chauvin ◽  
R. Dean Astumian

Recent experiments show that membrane ATPases are capable of absorbing free energy from an applied oscillating electric field and converting it to chemical bond energy of ATP or chemical potential energy of concentration gradients. Presumably these enzymes would also respond to endogenous transmembrane electric fields of similar intensity and waveform. A mechanism is proposed in which energy coupling is achieved via Coulombic interaction of an electric field and the conformational equilibria of an ATPase. Analysis indicates that only an oscillating or fluctuating electric field can be used by an enzyme to drive a chemical reaction away from equilibrium. In vivo, the stationary transmembrane potential of a cell must be modulated to become “locally” oscillatory if it is to derive energy and signal transduction processes.

2003 ◽  
Vol 773 ◽  
Author(s):  
Shalini Prasad ◽  
Mo Yang ◽  
Xuan Zhang ◽  
Yingchun Ni ◽  
Vladimir Parpura ◽  
...  

AbstractCharacterization of electrical activity of individual neurons is the fundamental step in understanding the functioning of the nervous system. Single cell electrical activity at various stages of cell development is essential to accurately determine in in-vivo conditions the position of a cell based on the procured electrical activity. Understanding memory formation and development translates to changes in the electrical activity of individual neurons. Hence, there is an enormous need to develop novel ways for isolating and positioning individual neurons over single recording sites. To this end, we used a 3x3 multiple microelectrode array system to spatially arrange neurons by applying a gradient AC field. We characterized the electric field distribution inside our test platform by using two dimensiona l finite element modeling (FEM) and determined the location of neurons over the electrode array. Dielectrophoretic AC fields were utilized to separate the neurons from the glial cells and to position the neurons over the electrodes. The neurons were obtained from 0-2-day-old rat (Sprague-Dawley) pups. The technique of using electric fields to achieve single neuron patterning has implications in neural engineering, elucidating a new and simpler method to develop and study neuronal activity as compared to conventional microelectrode array techniques.


2002 ◽  
Vol 1 (5) ◽  
pp. 319-327 ◽  
Author(s):  
M. P. Rols ◽  
M. Golzio ◽  
B. Gabriel ◽  
J. Teissié

Electric field pulses are a new approach for drug and gene delivery for cancer therapy. They induce a localized structural alteration of cell membranes. The associated physical mechanisms are well explained and can be safely controlled. A position dependent modulation of the membrane potential difference is induced when an electric field is applied to a cell. Electric field pulses with an overcritical intensity evoke a local membrane alteration. A free exchange of hydrophilic low molecular weight molecules takes place across the membrane. A leakage of cytosolic metabolites and a loading of polar drugs into the cytoplasm are obtained. The fraction of the cell surface which is competent for exchange is a function of the field intensity. The level of local exchange is strongly controlled by the pulse duration and the number of successive pulses. The permeabilised state is long lived. Its lifetime is under the control of the cumulated pulse duration. Cell viability can be preserved. Gene transfer is obtained but its mechanism is not a free diffusion. Plasmids are electrophoretically accumulated against the permeabilised cell surface and form aggregates due to the field effect. After the pulses, several steps follow: translocation to the cytoplasm, traffic to the nucleus and expression. Molecular structural and metabolic changes in cells remain mostly poorly understood. Nevertheless, while most studies were established on cells in culture ( in vitro), recent experiments show that similar effects are obtained on tissue ( in vivo). Transfer remains controlled by the physical parameters of the electrical treatment.


2019 ◽  
Author(s):  
Ehsan Negahbani ◽  
Iain M. Stitt ◽  
Marshall Davey ◽  
Thien T. Doan ◽  
Moritz Dannhauer ◽  
...  

SummaryModeling studies predict that transcranial alternating current stimulation (tACS) entrains brain oscillations, yet direct examination has been lacking or potentially contaminated by stimulation artefact. Here we first demonstrate how the posterior parietal cortex drives primary visual cortex and thalamic LP in the alpha-band in head-fixed awake ferrets. The spike-field synchrony is maximum within alpha frequency, and more prominent for narrow-spiking neurons than broad-spiking ones. Guided by a validated model of electric field distribution, we produced electric fields comparable to those in humans and primates (< 0.5 mV/mm). We found evidence to support the model-driven predictions of how tACS entrains neural oscillations as explained by the triangular Arnold tongue pattern. In agreement with the stronger spike-field coupling of narrow-spiking cells, tACS more strongly entrained this cell population. Our findings provide the firstin vivoevidence of how tACS with electric field amplitudes used in human studies entrains neuronal oscillators.


2014 ◽  
Vol 136 (9) ◽  
Author(s):  
Mary Phillips

Nonthermal irreversible electroporation (NTIRE) is an ablation modality that utilizes microsecond electric fields to produce nanoscale defects in the cell membrane. This results in selective cell death while preserving all other molecules, including the extracellular matrix. Here, finite element analysis and experimental results are utilized to examine the effect of NTIRE on the small intestine due to concern over collateral damage to this organ during NTIRE treatment of abdominal cancers. During previous studies, the electrical treatment parameters were chosen based on a simplified homogeneous tissue model. The small intestine, however, has very distinct layers, and a more realistic model is needed to further develop this technology for precise clinical applications. This study uses a two-dimensional finite element solution of the Laplace and heat conduction equations to investigate how small intestine heterogeneities affect the electric field and temperature distribution. Experimental results obtained by applying NTIRE to the rat small intestine in vivo support the heterogeneous effect of NTIRE on the tissue. The numerical modeling indicates that the electroporation parameters chosen for this study avoid thermal damage to the tissue. This is supported by histology obtained from the in vivo study, which showed preservation of extracellular structures. The finite element model also indicates that the heterogeneous structure of the small intestine has a significant effect on the electric field and volume of cell ablation during electroporation and could have a large impact on the extent of treatment. The heterogeneous nature of the tissue should be accounted for in clinical treatment planning.


2022 ◽  
Author(s):  
Ran An ◽  
Adrienne Minerick

The ability to generate stable, spatiotemporally controllable concentration gradients is critical for both electrokinetic and biological applications such as directional wetting and chemotaxis. Electrochemical techniques for generating solution and surface gradients display benefits such as simplicity, controllability, and compatibility with automation. Here, we present an exploratory study for generating micro-scale spatiotemporally controllable gradients using a reaction-free electrokinetic technique in a microfluidic environment. Methanol solutions with ionic Fluorescein isothiocyanate (FITC) molecules were used as an illustrative electrolyte. Spatially non-uniform alternating current (AC) electric fields were applied using hafnium dioxide (HfO2) coated Ti/Au electrode pairs. Results from spatial and temporal analysis, along with control experiments suggest that the FITC ion concentration gradient in bulk fluid (over 50 µm from the electrode) was established due to spatial variation of electric field density, and was independent of electrochemical reactions at the electrode surface. The established ion concentration gradients depended on both amplitudes and the frequencies of the oscillating AC electric field. Overall, this work reports a novel approach for generating stable and spatiotemporally tunable gradients in a microfluidic chamber using a reaction-free electrochemical methodology.


2006 ◽  
Author(s):  
Bing Song ◽  
Jin Pu ◽  
Brian Reid ◽  
Zhiqiang Zhao ◽  
Min Zhao

2022 ◽  
Author(s):  
Ran An ◽  
Adrienne Minerick

The ability to generate stable, spatiotemporally controllable concentration gradients is critical for both electrokinetic and biological applications such as directional wetting and chemotaxis. Electrochemical techniques for generating solution and surface gradients display benefits such as simplicity, controllability, and compatibility with automation. Here, we present an exploratory study for generating micro-scale spatiotemporally controllable gradients using a reaction-free electrokinetic technique in a microfluidic environment. Methanol solutions with ionic Fluorescein isothiocyanate (FITC) molecules were used as an illustrative electrolyte. Spatially non-uniform alternating current (AC) electric fields were applied using hafnium dioxide (HfO2) coated Ti/Au electrode pairs. Results from spatial and temporal analysis, along with control experiments suggest that the FITC ion concentration gradient in bulk fluid (over 50 µm from the electrode) was established due to spatial variation of electric field density, and was independent of electrochemical reactions at the electrode surface. The established ion concentration gradients depended on both amplitudes and the frequencies of the oscillating AC electric field. Overall, this work reports a novel approach for generating stable and spatiotemporally tunable gradients in a microfluidic chamber using a reaction-free electrochemical methodology.


1996 ◽  
Vol 76 (6) ◽  
pp. 4202-4205 ◽  
Author(s):  
B. J. Gluckman ◽  
E. J. Neel ◽  
T. I. Netoff ◽  
W. L. Ditto ◽  
M. L. Spano ◽  
...  

1. The effects of relatively small external DC electric fields on synchronous activity in CA1 and CA3 from transverse and longitudinal type hippocampal slices were studied. 2. To record neuronal activity during significant field changes, differential DC amplification was employed with a reference electrode aligned along an isopotential with the recording electrode. 3. Suppression of epileptiform activity was observed in 31 of 33 slices independent of region studied and type of slice but was highly dependent on field orientation with respect to the apical dendritic-somatic axis. 4. Modulation of neuronal activity in these experiments was readily observed at field strengths < or = 5–10 mV/mm. Suppression was seen with the field oriented (positive to negative potential) from the soma to the apical dentrites. 5. In vivo application of these results may be feasible.


2007 ◽  
Vol 2 (6) ◽  
pp. 1479-1489 ◽  
Author(s):  
Bing Song ◽  
Yu Gu ◽  
Jin Pu ◽  
Brian Reid ◽  
Zhiqiang Zhao ◽  
...  

Author(s):  
Raul I. Garcia ◽  
Evelyn A. Flynn ◽  
George Szabo

Skin pigmentation in mammals involves the interaction of epidermal melanocytes and keratinocytes in the structural and functional unit known as the Epidermal Melanin Unit. Melanocytes(M) synthesize melanin within specialized membrane-bound organelles, the melanosome or pigment granule. These are subsequently transferred by way of M dendrites to keratinocytes(K) by a mechanism still to be clearly defined. Three different, though not necessarily mutually exclusive, mechanisms of melanosome transfer have been proposed: cytophagocytosis by K of M dendrite tips containing melanosomes, direct injection of melanosomes into the K cytoplasm through a cell-to-cell pore or communicating channel formed by localized fusion of M and K cell membranes, release of melanosomes into the extracellular space(ECS) by exocytosis followed by K uptake using conventional phagocytosis. Variability in methods of transfer has been noted both in vivo and in vitro and there is evidence in support of each transfer mechanism. We Have previously studied M-K interactions in vitro using time-lapse cinemicrography and in vivo at the ultrastructural level using lanthanum tracer and freeze-fracture.


Sign in / Sign up

Export Citation Format

Share Document