Dipole Potential Research Articles

The first principle calculations of band offsets among Cs2(Ti, Zr, Hf)X6 double halide perovskites

This study investigates the band offsets among Cs2(Ti, Zr, Hf)X6 double halide perovskites. Valence band offsets (VBO) and conduction band offsets (CBO) were calculated using density functional theory (DFT) with the Perdew–Burke-Ernzerhof (PBE) functional and the hybrid Heyd–Scuseria–Ernzerhof (HSE) functional, employing the supercell technique. This technique offers greater accuracy and reliability by explicitly calculating the potential differences at the interface. A critical factor influencing the results is the contribution of the dipole potential (VD), which induces shifts in the VBO and CBO by approximately 0.2 to 0.6 eV relative to values predicted by the electron affinity rule. This discrepancy arises from the inclusion of interface-specific effects, such as charge redistribution and polarization. Additionally, the findings indicate that the energy band alignments among these compounds are type-I within the same group of halides, with nearly identical lattice constants for Zr- and Hf-based compounds due to their similar ionic radii. These results provide valuable insights for the design of heterostructures in electronic applications and highlight the potential of Cs2(Ti, Zr, Hf)X6 compounds as efficient materials for solar cells, light-emitting diodes, and photodetectors.

The Membrane Dipole Potential and the Roles of Interfacial Water and Lipid Hydrocarbon Chains.

Understanding membrane charge transport processes, including the actions of ion channels, pumps, carriers, and membrane-active peptides, requires a description of the electrostatics of the lipid bilayer. We have simulated a library of different lipid chemistries to reveal the impact of the headgroup, glycerol backbone, and hydrocarbon chains on the membrane dipole potential. We found a strong dependence of the potential on lipid packing, but this was not caused by the packing of lipid polar components, due to cancellation of their electric fields by electrolyte. In contrast, lipid tail contributions were determined by area per lipid, arising from two countering effects. Increased area per lipid leads to chain tilting that increases methylene dipole projections to strengthen the electric field within the bilayer, while at the same time decreasing the electric field from terminal methyl groups. Moreover, electric fields from some nonterminal groups and the terminal methyl group can extend beyond the bilayer center and be canceled by the opposing leaflet. This interleaflet field annulment explains the experimental reduction in dipole potential for unsaturated and branched lipid bilayers, by as much as ∼200 mV, as well as experiments that substitute chain carbons with sulfur. Replacing ester with ether groups (eliminating two carbonyl groups) causes a significant reduction in potential, also by ∼200 mV, in agreement with experiment. We show that the effect can be largely attributed to the loss of aligned water molecules in the glycerol backbone region, lowering the potential inside the bilayer core. When only one of the two carbonyls is removed (using a hybrid ester-ether lipid or a single-chain lipid), most of this reduction in potential was lost, with the single carbonyl group able to maintain full hydration in the interfacial region. While headgroup chemistry can have a major effect (by as much as ±100 mV relative to phosphatidylcholine), anionic headgroups either decrease or increase the dipole potential, with the variation involving perturbation in hydrogen-bonded water molecules and changes in packing of lipid tails. Overall, these results suggest that membrane electrostatics are dominated by aligned water molecules at the polar-hydrocarbon interface and, surprisingly, by the charge distribution of the nonpolar lipid tails, and not the packing of headgroup and glycerol carbonyl dipoles.

Lipid Specificity of the Fusion of Bacterial Extracellular Vesicles with the Host Membrane.

Bacterial membrane vesicles (MVs) facilitate the long-distance delivery of virulence factors crucial for pathogenicity. The entry and trafficking mechanisms of virulence factors inside host cells are recently emerging; however, whether bacterial MVs can fuse and modulate the physicochemical properties of the host lipid membrane and membrane lipid parameter for fusion remains unknown. In this study, we reconstituted the interaction of bacterial MVs with host cell lipid membranes and quantitatively showed that bacterial MV interaction increases the fluidity, dipole potential, and compressibility of a biologically relevant multicomponent host membrane upon fusion. The presence of cylindrical lipids, such as phosphatidylcholine, and a moderate acyl chain length of C16 help the MV interaction. While significant binding of bacterial MVs to the raft-like lipid membranes with phase-separated regions of the membrane was observed, however, MVs prefer binding to the liquid-disordered regions of the membrane. Furthermore, the elevated levels of cholesterol tend to hinder the interaction of bacterial MVs, as evident from the favorable excess Gibbs free energy of mixing bacterial MVs with host lipid membranes. The findings provide new insights that might have implications for the regulation of host machinery by bacterial pathogens through manipulation of the host membrane properties.

Vortex-pair dynamics in three-dimensional homogeneous dipolar superfluids

The static and dynamic properties of vortices in dipolar Bose-Einstein condensates (dBECs) can be considerably modified relative to their nondipolar counterparts by the anisotropic and long-ranged nature of the dipole-dipole interaction. Working in a uniform dBEC, we analyze the structure of single vortices and the dynamics of vortex pairs, investigating the deviations from the nondipolar paradigm. For a straight vortex line, we find that the induced dipolar interaction potential is axially anisotropic when the dipole moments have a nonzero projection orthogonal to the vortex line. This results in a corresponding elongation of the vortex core along this projection as well as an anisotropic superfluid phase and enhanced compressibility in the vicinity of the vortex core. Consequently, the trajectories of like-signed vortex pairs are described by a family of elliptical and oval-like curves rather than the familiar circular orbits. Similarly for opposite-signed vortex pairs their translation speeds along the binormal are found to be dipole-interaction dependent. We expect that these findings will shed light on the underlying mechanisms of many-vortex phenomena in dBECs such as quantum turbulence, vortex reconnections, and vortex lattices. Published by the American Physical Society 2024

Revealing the regulation of water dipole potential to aggregation of amyloid‐β 42 at chiral interface by surface‐enhanced infrared absorption spectroscopy

AbstractSurface chirality plays an important role in determining the biological effect, but the molecular nature beyond stereoselectivity is still unknown. Herein, through surface‐enhanced infrared absorption spectroscopy, electrochemistry, and theoretical simulations, we found diasteromeric monolayers induced by assembled density on chiral gold nanofilm and identified the positive contribution of water dipole potential at chiral interface and their different interfacial interactions, which result in a difference both in the positive dipoles of interfacial water compensating the negative surface potential of the SAM and in the hindrance effect of interface dehydration, thereby regulating the interaction between amyloid‐β peptide (Aβ) and N‐isobutyryl‐cysteine (NIBC). Water on L‐NIBC interface which shows stronger positive dipole potential weakens the negative surface potential, but its local weak binding to the isopropyl group facilitates hydrophobic interaction between Aβ42 and L‐NIBC and resulted fiber aggregate. Conversely, electrostatic interaction between Aβ42 and D‐NIBC induces spherical oligomer. These findings provide new insight into molecular nature of chirality‐regulated biological effect.

Controlling the interactions in a cold atom quantum impurity system

We implement an experimental architecture in which a single atom of K is trapped in an optical tweezer, and is immersed in a bath of Rb atoms at ultralow temperatures. In this regime, the motion of the single trapped atom is confined to the lowest quantum vibrational levels. This realizes an elementary and fully controllable quantum impurity system. For the trapping of the K atom, we use a species-selective dipole potential, that allows us to independently manipulate the quantum impurity and the bath. We concentrate on the characterization and control of the interactions between the two subsystems. To this end, we perform Feshbach spectroscopy, detecting several inter-dimensional confinement-induced Feshbach resonances for the KRb interspecies scattering length, that parametrizes the strength of the interactions. We compare our data to a theory for inter-dimensional scattering, finding good agreement. Notably, we also detect a series of p-wave resonances stemming from the underlying free-space s-wave interactions. We further determine how the resonances behave as the temperature of the bath and the dimensionality of the interactions change. Additionally, we are able to screen the quantum impurity from the bath by finely tuning the wavelength of the light that produces the optical tweezer, providing us with a new effective tool to control and minimize the interactions. Our results open a range of new possibilities in quantum simulations of quantum impurity models, quantum information, and quantum thermodynamics, where the interactions between a quantized system and the bath is a powerful yet largely underutilized resource.

Ergosterol promotes aggregation of natamycin in the yeast plasma membrane

Polyene macrolides are antifungal substances, which interact with cells in a sterol-dependent manner. While being widely used, their mode of action is poorly understood. Here, we employ ultraviolet-sensitive (UV) microscopy to show that the antifungal polyene natamycin binds to the yeast plasma membrane (PM) and causes permeation of propidium iodide into cells. Right before membrane permeability became compromised, we observed clustering of natamycin in the PM that was independent of PM protein domains. Aggregation of natamycin was paralleled by cell deformation and membrane blebbing as revealed by soft X-ray microscopy. Substituting ergosterol for cholesterol decreased natamycin binding and caused a reduced clustering of natamycin in the PM. Blocking of ergosterol synthesis necessitates sterol import via the ABC transporters Aus1/Pdr11 to ensure natamycin binding. Quantitative imaging of dehydroergosterol (DHE) and cholestatrienol (CTL), two analogues of ergosterol and cholesterol, respectively, revealed a largely homogeneous lateral sterol distribution in the PM, ruling out that natamycin binds to pre-assembled sterol domains. Depletion of sphingolipids using myriocin increased natamycin binding to yeast cells, likely by increasing the ergosterol fraction in the outer PM leaflet. Importantly, binding and membrane aggregation of natamycin was paralleled by a decrease of the dipole potential in the PM, and this effect was enhanced in the presence of myriocin. We conclude that ergosterol promotes binding and aggregation of natamycin in the yeast PM, which can be synergistically enhanced by inhibitors of sphingolipid synthesis.

Impact of defect concentration on piezoelectricity in Mn/Fe-doped KTN crystals

Defect engineering via doping exhibits considerable potential for improving the performance of environment-friendly lead-free piezoelectric materials. Owing to the susceptibility to lattice vibrations and the micro-local chemical environment, the readily available Mn/Fe transition metal elements (TMEs) facilitate the construction of defect structures. However, the role of TMEs in shaping the domain structures and the corresponding promotional mechanism of piezoelectricity need to be further decoded. Herein, we propose the different influence mechanisms of Mn and Fe ions on the ferroelectric domain and piezoelectric properties. Different concentrations of (MnNb/Ta′-VO••)• and (FeNb/Ta″-VO••)× defect dipoles are obtained based on the synergy of Mn/Fe ions with oxygen vacancies. Diverse ferroelectric behaviors resulting from (MnNb/Ta′-VO••)• and (FeNb/Ta″-VO••)× defect dipoles are observed. Furthermore, the variation of the dielectric diffusiveness with the defect dipole concentration is investigated. Trace concentration of (MnNb/Ta′-VO••)• generates strong diffusiveness. With the characterization of the ferroelectric domain, this strong diffusiveness is attributed to the lattice-like domain structure. Thereafter, the mechanisms of Mn/Fe defect dipoles on the formation of domain structures are clarified. Macroscopically, the dielectric and piezoelectric properties are measured with Mn/Fe ion components. Trace Mn doping and the resulting lattice-like domain significantly enhance the piezoelectric coefficient, resulting in an increase of nearly 50% for K(Ta,Nb)O3 single crystals. This work highlights the tremendous potential of TME-induced defect dipoles for modifying the ferroelectric domain and provides a reference paradigm for improving piezoelectricity through defect engineering.

Cholesterol Changes Interfacial Water Alignment in Model Cell Membranes.

The nanoscopic layer of water that directly hydrates biological membranes plays a critical role in maintaining the cell structure, regulating biochemical processes, and managing intermolecular interactions at the membrane interface. Therefore, comprehending the membrane structure, including its hydration, is essential for understanding the chemistry of life. While cholesterol is a fundamental lipid molecule in mammalian cells, influencing both the structure and dynamics of cell membranes, its impact on the structure of interfacial water has remained unknown. We used surface-specific vibrational sum-frequency generation spectroscopy to study the effect of cholesterol on the structure and hydration of monolayers of the lipids 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), and egg sphingomyelin (SM). We found that for the unsaturated lipid DOPC, cholesterol intercalates in the membrane without significantly changing the orientation of the lipid tails and the orientation of the water molecules hydrating the headgroups of DOPC. In contrast, for the saturated lipids DPPC and SM, the addition of cholesterol leads to clearly enhanced packing and ordering of the hydrophobic tails. It is also observed that the orientation of the water hydrating the lipid headgroups is enhanced upon the addition of cholesterol. These results are important because the orientation of interfacial water molecules influences the cell membranes' dipole potential and the strength and specificity of interactions between cell membranes and peripheral proteins and other biomolecules. The lipid nature-dependent role of cholesterol in altering the arrangement of interfacial water molecules offers a fresh perspective on domain-selective cellular processes, such as protein binding.

Loading atoms from a large magnetic trap to a small intra-cavity optical lattice

We show that an optimized loading of a cold ensemble of rubidium-87 atoms from a magnetic trap into an optical lattice sustained by a single, far-red-detuned mode of a high-Q optical cavity can be efficient despite the large volume mismatch of the traps. The magnetically trapped atoms are magnetically transported to the vicinity of the cavity mode and released from the magnetic trap in a controlled way meanwhile undergoing an evaporation period. Large number of atoms get trapped in the dipole potential of the cavity mode for several hundreds of milliseconds. We monitor the number of atoms in the mode volume by a second tone of the cavity close to the atomic resonance. While this probe tone can pump atoms to another ground state uncoupled to the probe, we demonstrate state-independent trapping by applying a repumper laser.

Sensing Characteristics of SARS-CoV-2 Spike Protein Using Aptamer-Functionalized Si-Based Electrolyte-Gated Field-Effect Transistor (EGT).

The sensing responses of SARS-CoV-2 spike protein using top-down-fabricated Si-based electrolyte-gated transistors (EGTs) have been investigated. An aptamer was employed as a receptor for the SARS-CoV-2 spike protein. The EGT demonstrated excellent intrinsic characteristics and higher sensitivity in the subthreshold regime compared to the linear regime. The limit of detection (LOD) was achieved as low as 0.94 pg/mL and 20 pg/mL for the current and voltage sensitivity, respectively. To analyze the sensing responses of EGT in detecting the aptamer-SARS-CoV-2 spike protein conjugate, a lumped-capacitive model with the presence of an effective dipole potential and an effective capacitance of the functionalized layer component was employed. The aptamer-functionalized EGT showed high sensitivity even in 10 mM phosphate-buffered saline (PBS) solution. These results suggest that Si-based EGTs are a highly promising method for detecting SARS-CoV-2 spike proteins.

Manipulating polarization effect in nonsequential double ionization.

We report on a theoretical study of nonsequential double ionization (NSDI) of magnesium atoms by using combined linearly and circularly polarized fields. By employing a concise model including the dynamic ionic dipole potential, we show that the polarization effects can be controlled by tuning the subcycle waveform of the electric field of the two-color pulses. We demonstrate that the influence of the dipole potential on NSDI depends on the symmetry of two-color laser fields by tracing back the electron trajectories. Furthermore, we propose a method allowing for manipulating the returning trajectories with the initial direction of the tunneled electrons almost unchanged.

Sensing cholesterol-induced rigidity in model membranes with time-resolved fluorescence spectroscopy and microscopy.

Here, we report the characterization of cholesterol levels on membrane fluidity with a twisted intramolecular charge transfer (TICT) membrane dye, namely DI-8-ANEPPS, using fluorescence lifetime techniques such as time-correlated single photon counting (TCSPC) and fluorescence lifetime imaging microscopy (FLIM). The characterized liposomes comprised a 3 : 1 ratio of POPC and POPG, respectively, 1% DI-8-ANEPPS, and increasing cholesterol levels from 0% to 50%. Fluorescence lifetime characterization revealed that increasing the cholesterol levels from 0% to 50% increases the fluorescence lifetime of DI-8-ANEPPS from 2.36 ns to 3.65 ns, a 55% increment. Such lengthening in the fluorescence lifetime is concomitant with reduced Stokes shifts and higher quantum yield, revealing that localized excitation (LE) dominates over TICT states with increased cholesterol levels. Fluorescence anisotropy measurements revealed a less isotropic environment in the membrane upon increasing cholesterol levels, suggesting a shift from liquid-disorder (Lα) to liquid-order (LO) upon adding cholesterol. Local electrostatic and dipole characterization experiments revealed that changes in the zeta-potential (ζ-potential) and transmembrane dipole potential (Ψd) induced by changes in cholesterol levels or the POPC : POPG ratio play a minimal role in the fluorescence lifetime outcome of DI-8-ANEPPS. Instead, these results indicate that the cholesterol's effect in restricting the degree of movement of DI-8-ANEPPS dominates its photophysics over the cholesterol effect on the local dipole strength. We envision that time-resolved spectroscopy and microscopy, coupled with TICT dyes, could be a convenient tool in exploring the complex interplay between membrane lipids, sterols, and proteins and provide novel insights into membrane fluidity, organization, and function.

Structure and Elasticity of Mitochondrial Membranes: A Molecular Dynamics Simulation Study.

Mitochondria are known as the powerhouse of the cell because they produce energy in the form of adenosine triphosphate. They also have other crucial functions such as regulating apoptosis, calcium homeostasis, and reactive oxygen species production. To perform these diverse functions, mitochondria adopt specific structures and frequently undergo dynamic shape changes, indicating that their mechanical properties play an essential role in their functions. To gain a detailed understanding at the molecular level of the structure and mechanical properties of mitochondria, we carry out atomistic molecular dynamics simulations for three inner mitochondrial membranes and three outer mitochondrial membrane models. These models take into account variations in cardiolipin and cholesterol concentrations as well as the symmetry/asymmetry between the two leaflets. Our simulations allow us to calculate various structural quantities and the bending, twisting, and tilting elastic moduli of the membrane models. Our results indicate that the structures of the inner and outer mitochondrial membranes are quite similar and do not depend much on the variation in lipid compositions. However, the bending modulus of the membranes increases with increasing concentrations of cardiolipin or cholesterol but decreases with a membrane asymmetry. Notably, we found that the dipole potential of the membrane increases with an increasing cardiolipin concentration. Finally, possible roles of cardiolipin in regulating ion and proton currents and maintaining the cristate are discussed in some details.

Simulations and integral-equationtheories for dipolar density interacting disks.

Integral equationtheories (IETs) based on the Ornstein-Zernike (OZ) relation can be used as an analytical tool to predict structural and thermodynamic properties and phase behavior of fluids with low numerical cost. However, there are no studies of the IETs for the dipolar density interaction potential in two-dimensional systems, a relevant interdomain interaction in lipid monolayers with phase coexistence. This repulsive interaction arises due to the excess dipole density of the domains, which are aligned perpendicular to the interface. This work studies the performance of three closures of the OZ equationfor this novel system: Rogers-Young (RY), modified hypernetted chain (MHNC), and variational modified hypernetted chain (VMHNC). For the last two closures the bridge function of a reference system is required, with the hard disk being the most convenient reference system. Given that in two dimensions there is no analytical expressions for the hard disk correlation functions, two different approximations are proposed: one based on the Percus-Yevick (PY) approximation, and the other based on an extension of the hard spheres Verlet-Weis-Henderson-Grundke (LB) parametrization. The accuracy of the five approaches is evaluated by comparison of the pair correlation function and the structure factor with Monte Carlo simulation data. The results show that RY closure is satisfactory only for low-structured regimes. MHNC and VMHNC closures perform globally well, and there are no significant differences between them. However, the reference system in some cases affects their performance; when the pair correlation function serves as the measure, the LB-based closures quantitatively outperform the PY ones. From the point of view of its applicability, LB-based closures do not have a solution for all studied interaction strength parameters, and, in general, PY-based closures are numerically preferable.

Compensating three-dimensional field inhomogeneity in cold atom Efimov-state search by a time-averaged optical potential.

The Efimov effect and its universal property are of paramount importance in quantum few-body physics. Despite this, the predicted ground state Efimov resonance has not yet been observed in 39,40,41K-87Rb mixtures within the currently available observation window. Cooling atoms in the microgravity environment of outer space might overcome this limitation, whereas the residual curvature of the strong magnetic fields may result in significant atom leakage. In this work, we propose an optical method based on far-detuned time-averaged dipole potential to counteract the three-dimensional inhomogeneous field. The target intensity distribution can be conveniently obtained by modulating the central position of the quasi-1D print beam using acoustic optical modulators. Within a volume of 300 × 300 × 400µm3, the residual potential fluctuations can be reduced by two orders of magnitude to less than 100 pK. The proposed approach offers a realistic prospect of investigating the Efimov-type resonance in the 40K-87Rb Bose-Fermi mixture.

Novel customized age-dependent corneal membranes and interactions with biodegradable nanoparticles loaded with dexibuprofen

Ocular inflammation is one of the most prevalent diseases in ophthalmology and it is currently treated using eye drops of nonsteroidal antiinflammatory drugs such as dexibuprofen (DXI). However, their bioavailability is low and therefore, PLGA nanoparticles constitute a suitable approach to be administered as eyedrops. Therefore, DXI has been encapsulated into PLGA nanoparticles (DXI-NPs). Although the eye, and specifically the cornea, suffers from age-related changes in its composition, current medications are not focused on these variations. Therefore, to elucidate the interaction mechanism of DXI-NPs with the cornea in relation with age, two different corneal membrane models have been developed (corresponding to adult and elder population) using lipid monolayers, large and giant unilamellar vesicles. Interactions of both DXI and DXI-NPs were studied with these models by means of Langmuir balance technique, dipole potential, anisotropy and confocal microscopy. In addition, fluorescently labelled nanoparticles were administered to mice in order to corroborate these data obtained in vitro. It was observed that DXI-NPs interact with lipid membranes through an adhesion process, mainly in the rigid regions and afterwards DXI-NPs are internalized by a wrapping process. Furthermore, differences on the dipole potential caused by DXI-NPs in each corneal membrane have been obtained due to the increase of membrane rigidity on the ECMM. Additionally, it can be confirmed that DXI-NPs adhere to Lo phase and also inside the lipid membrane. Finally, in vitro and in vivo results corroborate that DXI-NPs are adhered to the more ordered phase. Finally, differences between interactions of DXI-NPs with the elder and adult corneal tissue were observed.

Structure and elasticity of healthy and Alzheimer's disease cell membranes revealed by molecular dynamics simulations.

Interactions of amyloid-β (Aβ) peptides with neuronal membrane are associated with the development of Alzheimer's disease (AD). Ganglioside monosialotetrahexosylganglioside (GM1) lipids have been shown to form clusters that induce the structural conversion of Aβ and promote the incorporation of Aβ into the membrane via the membrane surface electrical potential. Prior to the onset of AD symptoms, GM1 clusters may not have formed but the concentration of GM1 may have already changed, and our question is whether this early concentration modification affects the structure and mechanical properties of the membrane. Using one model for healthy cell membranes and three models for AD cell membranes, we carry out 2 µs all-atom molecular dynamics simulations for each model to compare the structure and elasticity of the two membrane types. The simulations show that at the physiological concentration, 1%-3%, GM1 does not form clusters. The reduction of the GM1 lipid does not significantly alter the area per lipid, the membrane thickness, and the lipid order parameters of the AD membranes. However, the dipole potential, the bending, and twist moduli are decreased for the AD membranes. We suggest that these changes in the AD membranes are factors that could trigger the interaction and incorporation of Aβ to the membranes. Finally, we show that changes in the sphingomyelin lipid concentrations do not affect the membrane structure and elasticity.

Optimizing Optical Potentials With Physics-Inspired Learning Algorithms

We present our experimental and theoretical framework, which combines a broadband superluminescent diode with fast learning algorithms to provide speed and accuracy improvements for the optimization of on-dimensional optical dipole potentials, here generated with a digital micromirror device. To characterize the setup and potential speckle patterns arising from coherence, we compare the superluminescent diode to a single-mode laser by investigating interference properties. We employ machine-learning tools to train a physics-inspired model acting as a digital twin of the optical system predicting the behavior of the optical apparatus including all its imperfections. Implementing an iterative algorithm based on iterative learning control we optimize optical potentials an order of magnitude faster than heuristic optimization methods. We compare iterative model-based ``offline'' optimization and experimental feedback-based ``online'' optimization. Our methods provide a route to fast optimization of optical potentials, which is relevant for the dynamical manipulation of ultracold gases.

Modulation of the Dipole Potential of Model Lipid Membranes with Phytochemicals: Molecular Mechanisms, Structure-Activity Relationships, and Implications in Reconstituted Ion Channels.

Phytochemicals, such as flavonoids, stilbenoids, alkaloids, terpenoids, and related compounds, have a wide range of useful pharmacological properties which cannot be ascribed to binding to a single peptide or protein target alone. Due to the relatively high lipophilicity of phytochemicals, the lipid membrane is thought to mediate their effects via changes in the properties of the lipid matrix, in particular, by modulating the transmembrane distribution of the electrical potential and, consequently, the formation and functioning of the ion channels reconstituted in the lipid bilayers. Therefore, biophysical studies on the interactions between plant metabolites and model lipid membranes are still of interest. This review represents an attempt to provide a critical analysis of a variety of studies on altering membranes and ion channels with phytochemicals via disturbing the potential drop at the membrane-aqueous solution interface. Critical structural motifs and functioning groups in the molecules of plant polyphenols (alkaloids and saponins are identified) and the possible mechanisms of dipole potential modulation with phytochemicals are discussed.