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At least 325 records · Page 18Linked to original sources
PubMed2002

Salt effect on volume phase transition of a gel.

The salt effect on the phase transition of N-isopropylacrylamide (NIPA) gel was studied for alkali-metal chlorides (NaCl, KCl, and CsCl). Low-frequency Raman scattering experiment was conducted to know the dynamic state of water molecule under the presence of salt and its correlation to macroscopic phase behavior of the gel was investigated together with the thermodynamic activities of water molecule of aqueous alkali-metal chloride solutions. The series of swelling experiment reveal that the change in the gel volume phase transition strongly depends on the salt concentration and is related to the dehydration with respect to hydrophobic hydration. From the analysis of the reduced low-frequency Raman spectra in water and aqueous alkali-metal chlorides solutions by the use of the relaxation mode that takes into account the inertia and the non-white effects, the characteristic values of aqueous salt solutions (i.e., relaxation time and modulation speed) indicate that the addition of alkali-metal chloride to gel fluid affects the disruption of water molecules in the hydration shell around the NIPA gel and the formation of the hydrogen-bonded network structure of water around themselves, as a result of which the gel collapses. The chemical potential and the dynamic nature of water molecule at the transition points are well correlated: the chemical potentials at the transition points are almost constant whereas the structure of bulk water is changed by addition of alkali-metal chlorides or change in temperature. These results strongly suggest that the swelling ratio of N-isopropylacrylamide gel is a function of hydration degree, which is regulated by the chemical potential of water.

Journal Article↗
PubMed2005

Surface-induced phase transitions in ultrathin films of block copolymers.

We study theoretically the lamellar-disorder-lamellar phase transitions of AB diblock and tetrablock copolymers confined in symmetric slitlike pores where the planar surface discriminatingly adsorbs A segments but repels B segments, mimicking the hydrophobic/hydrophilic effects that have been recently utilized for the fabrication of environmentally responsive "smart" materials. The effects of film thickness, polymer volume fraction, and backbone structure on the surface morphology have been investigated using a polymer density-functional theory. The surface-induced phase transition is manifested itself in a discontinuous switch of microdomains or a jump in the surface density dictated by the competition of surface adsorption and self-aggregation of the block copolymers. The surface-induced first-order phase transition is starkly different from the thickness-induced symmetric-asymmetric or horizontal-vertical transitions in thin films of copolymer melts reported earlier.

Journal Article↗
PubMed2002

Transbilayer movement of phospholipids at the main phase transition of lipid membranes: implications for rapid flip-flop in biological membranes.

The transbilayer movement of fluorescent phospholipid analogs in liposomes was studied at the lipid phase transition of phospholipid membranes. Two NBD-labeled analogs were used, one bearing the fluorescent moiety at a short fatty acid chain in the sn-2 position (C(6)-NBD-PC) and one headgroup-labeled analog having two long fatty acyl chains (N-NBD-PE). The transbilayer redistribution of the analogs was assessed by a dithionite-based assay. We observed a drastic increase of the transbilayer movement of both analogs at the lipid phase transition of DPPC (T(c) = 41 degrees C) and DMPC (T(c) = 23 degrees C). The flip-flop of analogs was fast at the T(c) of DPPC with a half-time (t(1/2)) of ~6-10 min and even faster at the T(c) of DMPC with t(1/2) on the order of <2 min, as shown for C(6)-NBD-PC. Suppressing the phase transition by the addition of cholesterol, the rapid transbilayer movement was abolished. Molecular packing defects at the phase transition are assumed to be responsible for the rapid transbilayer movement. The relevance of those defects for understanding of the activity of flippases is discussed.

1,2-Dipalmitoylphosphatidylcholine↗
PubMedDate not supplied

Does membrane lipid profile explain chilling sensitivity and membrane lipid phase transition of spermatozoa and oocytes?

Ram, fowl and bee spermatozoa, and oocytes of cows and zebrafish were used to study lipid membrane profiles, chilling sensitivity and lipid-phase transitions. The integrity of the membranes was determined by carboxyfluorescein diacetate (CFDA) staining following exposure for 15 minutes to low temperatures. Ram and fowl spermatozoa showed different degrees of loss of membrane integrity. Surprisingly, bee spermatozoa did not show any sensitivity to chilling, and their membranes remained intact down to 0 degree C. In bovine oocytes (at the GV stage) chilling injury was very severe at 16 degree C (membrane integrity decreased by 50%). Lipid phase transition (LPT) and membrane fluidity, which were evaluated by Fourier transform infrared (FTIR) microscopy, and fluorescence polarisation, showed phase transitions at the same temperatures as caused damage (between 30 and 12 degree C). The membrane lipid profiles showed high concentrations of polyunsaturated fatty acids (PUFA) in cold-sensitive ram spermatozoa and zebrafish oocytes, but the ratio between PUFA and saturated fatty acids was highest in cold-resistant bee spermatozoa and lowest in cold-sensitive bovine oocytes. These results suggest a close relationship among cold susceptibility, lipid phase transition and lipids profile in animal gametes.

Journal Article↗
PubMed2001

Phase transitions and critical phenomena in the liquid bridge under lateral acceleration.

We study the shape of a liquid body under the influence of a lateral body force in a thin liquid bridge. The shape of the liquid body changes continuously or discontinuously depending on the volume of liquid body. We show that the transition from discontinuous to continuous change is described by the volume-induced phase transition driven by the lateral body force. The order parameter of the phase transition is the amount of shift of the center of mass of liquid body. Critical exponents of a mean-field model have been obtained by numerical calculation. We provide the validity of this critical behavior through the m(4) model of Landau theory of phase transition.

Journal Article↗
PubMed1986

Dynamic fluorescence measurements on the main phase transition of dipalmytoylphosphatidylcholine vesicles.

The kinetics of the main phase transition in dipalmytoylphosphatidylcholine (DPPC) vesicles have been investigated using our iodine laser-T-jump technique with fluorescence detection. A set of three fluorescent probes has been used to sense different parts of the bilayer hydrocarbon chain region. The well established membrane probes DPH and TMADPH as well as DPHPC, a labelled DPPC molecule. We report three relaxation signals in the microseconds and ms time range, which are detected with all three probes. This result supports our model of the main phase transition in DPPC vesicles.

1,2-Dipalmitoylphosphatidylcholine↗
PubMed2001

Kinetics and mechanism of the beta- to alpha-CuAlCl(4) phase transition: a time-resolved (63)Cu MAS NMR and powder X-ray diffraction study.

The beta and alpha phases of CuAlCl(4) have been characterized by solid-state (27)Al and (63)Cu magic angle spinning nuclear magnetic resonance. The very short spin--lattice relaxation times of the copper spins, and the sensitivity of the I = 3/2 (63)Cu nucleus to the small differences in the local structure of Cu in the two phases, allowed (63)Cu spectra to be acquired in very short time periods (1 min), in which the beta and alpha phases were clearly resolved. This time resolution was exploited to follow the phase transition from the pseudohexagonal close-packed beta-CuAlCl(4) into the pseudocubic close-packed alpha-CuAlCl(4), which occurs above 100 degrees C. In situ time-resolved (63)Cu MAS NMR and synchrotron X-ray diffraction experiments were used to measure the kinetics of this phase transition as a function of temperature. The transformation was shown to be a first-order phase transition involving no intermediate phases with an activation energy of 138 kJ/mol. The kinetic data obey a first-order Avrami--Erofe'ev rate law. A one-dimensional growth mechanism is proposed that involves a combination of Cu(+) ion self-diffusion and a translational reorganization of the close-packed anion layers imposed by the periodic rotations of [AlCl(4)](-) tetrahedra. This beta to alpha phase transformation can be induced at ambient temperatures by low partial pressures of ethylene.

Journal Article↗
PubMed1983

Effects of pressure and temperature on the M412 intermediate of the bacteriorhodopsin photocycle. Implications for the phase transition of the purple membrane.

The effects of pressure and temperature on the decay kinetics of the M412 (M) intermediate in the photocycle of bacteriorhodopsin were studied to provide information about the phase transitions of the purple membrane lipids. The activation volume (delta V++) for the decay of M is expected to be different below and above a phase transition. However, no abrupt change in delta V++ was found from 3.5 degrees to 60 degrees C. But a sharp break was observed in a plot of the logarithm of the rate of M decay vs. pressure. Extrapolation of this break point to standard atmospheric pressure gives a temperature of -42 degrees C, which probably corresponds to the phase transition of the purple membrane lipids. This conclusion is supported by studies of the effect of pressure on the M kinetics of bacteriorhodopsin incorporated into dimyristoylphosphatidylcholine vesicles, whose phase transition has previously been characterized.

Bacteriorhodopsins↗
PubMed1999

Coupling between a first-order gas-liquid phase transition and a second-order orientational transition in Langmuir monolayers.

The Ginzburg-Landau theory is developed to investigate coupling between a gas-liquid first-order phase transition (FOPT) and an orientational second-order phase transition (SOPT) in Langmuir monolayers. It is found that the coupled SOPT and FOPT takes place simultaneously if the uncoupled FOPT occurs prior to the SOPT with compression, and that in the opposite case, the coupling makes the FOPT take place at a lower pressure, but still behind the SOPT. Gas-liquid phase separation always leads to a decrease in the averaged order parameter of the orientational phase transition, which is qualitatively consistent with experimental data.

Journal Article↗
PubMed2000

Hamiltonian dynamics and geometry of phase transitions in classical XY models

The Hamiltonian dynamics associated with classical, planar, Heisenberg XY models is investigated for two- and three-dimensional lattices. In addition to the conventional signatures of phase transitions, here obtained through time averages of thermodynamical observables in place of ensemble averages, qualitatively different information is derived from the temperature dependence of Lyapunov exponents. A Riemannian geometrization of Newtonian dynamics suggests consideration of other observables of geometric meaning tightly related to the largest Lyapunov exponent. The numerical computation of these observables--unusual in the study of phase transitions--sheds light on the microscopic dynamical counterpart of thermodynamics, also pointing to the existence of some major change in the geometry of the mechanical manifolds at the thermodynamical transition. Through the microcanonical definition of the entropy, a relationship between thermodynamics and the extrinsic geometry of the constant energy surfaces sigma E of phase space can be naturally established. In this framework, an approximate formula is worked out determining a highly nontrivial relationship between temperature and topology of sigma E. From this it can be understood that the appearance of a phase transition must be tightly related to a suitable major topology change of sigma E. This contributes to the understanding of the origin of phase transitions in the microcanonical ensemble.

Journal Article↗
PubMed2003

Mri measurements of T1, T2 and D for gels undergoing volume phase transition.

Gels consist of crosslinked polymer network swollen in solvent. The network of flexible long-chain molecules traps the liquid medium they are immersed in. Some gels undergo abrupt volume change, a phase transition process, by swelling-shrinking in response to external stimuli changes in solvent composition, temperature, pH, electric field, etc. We report that during volume phase transition changes of NMR longitudinal relaxation time T(1), NMR transverse relaxation time T(2), and diffusion coefficient D of the PMMA gel, and D of the NIPA gel. We describe how the gels were synthesized and the reason of using the snapshot FLASH imaging sequence to measure T(1), T(2), and D. Since T(1), T(2) and D maps have identical field of view and data are extracted from identical areas from their respective maps, these values can be correlated quantitatively on a pixel-by-pixel basis. Thus a complete set of NMR parameters is measured in-situ: the gels are in their natural state, immersed in the liquid, during the phase transition. The results of spectroscopic method agree with that of snapshot FLASH imaging method. For the PMMA gel T(1), T(2) and D decrease when gels undergo volume phase transition between deuterated acetone concentration of 30% and 40%. At its contracted state, T(1) is reduced to a little less than one order of magnitude, T(2) over two orders of magnitude, and D over one order of magnitude, smaller from values of PMMA gel at the swollen state. At an elevated temperature of 54 degrees C the thermosensitive NIPA gel is at a contracted state, with its D reduced to almost one order of magnitude smaller from that of the swollen NIPA at room temperature.

Acrylamides↗
PubMed1989

[The action of membranotropic compounds with various structures on the parameters of the phase transition of dimyristoylphosphatidylcholine].

The effect of substances of different nature on the thermodynamic characteristics of dimyristoylphosphatidylcholine (DMPC) phase transition by the differential scanning microcalorimetry has been studied. The substances disposed in hydrophobic part of membrane--alpha-tocopherol, ubiquinone Q10, ionol and vitamin K3 cause the decrease of enthalpy and cooperativity of phase transition. The substances which have the side hydrocarbon chain (tocopherol and ubiquinone Q10) compared with ones without it (ionol and vitamin K3) and reduced quinones (Q10 and vitamin K3) compared with the oxidized ones have stronger influence on the enthalpy and cooperativity of transition. The inclusion of the local anesthetic dicaine disposed mainly in the zone of polar heads of phospholipids into DMPC membranes decreases the temperature of phase transition considerably and practically does not change the cooperativity. A possibility to use the method of differential scanning microcalorimetry to estimate the localization of membrane tropic substances within lipid bilayer is under discussion.

Butylated Hydroxytoluene↗
PubMed2004

Phase transitions in two planar lattice models and topological defects: a Monte Carlo study.

Monte Carlo simulation has been performed in the planar P2 and P4 models to investigate the effects of the suppression of topological defects on the phase transition exhibited by these models. Suppression of the 1/2 defects on the square plaquettes in the P2 model leads to complete elimination of the phase transition observed in this model. However, in the P4 model, on suppressing the single 1/2 defects on square plaquettes, the otherwise first order phase transition changes to a second order one which occurs at a higher temperature, and this is due to the presence of a large number of 1/2 pair defects which are left within the square plaquettes. When we suppressed these charges too, complete elimination of the phase transition was observed.

Journal Article↗
PubMed2002

Exact result on topology and phase transitions at any finite N.

We study analytically the topology of a family of submanifolds of the configuration space of the mean-field XY model, computing also a topological invariant (the Euler characteristic). We prove that a particular topological change of these submanifolds is connected to the phase transition of this system, and exists also at finite N. The present result is the first analytic proof that a phase transition has a topological origin and provides a key to a possible better understanding of the origin of phase transitions at their deepest level, as well as to a possible definition of phase transitions at finite N.

Journal Article↗
PubMed1999

Regulation of the G1/S transition phase in mesangial cells by E2F1.

It has been established that E2F transcription factors are essential for the regulation of the cell cycle. The E2Fs play an important role in G1/S transition phase, as they regulate the activation of several genes whose products are required for DNA synthesis. E2Fs bind to the retinoblastoma protein family and their transcriptional activities are suppressed in the G0 and early G1 phases. The E2F family consists of a group of five closely related proteins (E2F1 through E2F5). Proliferation of the mesangial cell is a common feature of many glomerular diseases, but the regulation of mesangial cell cycle has not been clarified, nor has the participation of the E2F family in mesangial cells. To elucidate the mechanisms of G1/S transition phase in mesangial cells, we investigated the roles of the E2F family in the mesangial cell cycle. In primary cultured mesangial cells, the protein expression of E2F1 through E2F3 was induced by fetal calf serum (FCS) stimulation. E2F1 especially was strongly induced by mitogenic stimulation. The E2F4 protein was abundantly expressed in the quiescent state and was slightly increased by FCS stimulation. We considered E2F1 to be representative of the E2F family, and used adenovirus-mediated gene transfer to investigate the function of E2F1 to show that overexpression of E2F1 promoted cell cycle progression as measured by a flow cytometer. Furthermore, we investigated the effect of E2F1 overexpression to cyclin D1 and cyclin E expression. Because we previously reported that the regulation of G1 cyclins is a key factor in the G1/S transition phase in mesangial cells, we showed that overexpression of E2F1 induced protein expression of cyclin D1 and cyclin E and increased promoter activity. Thus, we conclude that E2F1 plays an important role in the G1/S transition phase and acts on the mesangial cell cycle through two distinct pathways: (1) E2F1 directly transcribes an S-phase gene, and (2) E2F1 promotes cell cycle progression via the induction of cyclin D1 and cyclin E.

Animals↗
PubMed1990

Electric field increases the phase transition temperature in the bilayer membrane of phosphatidic acid.

The effect of the electric field on the phase transition temperature (Tc) of acidic 1,2-dipalmitoyl-sn-glycero-3-phosphate (DPPA) and 1,2-dipalmitoyl-sn-glycero-3-thionphosphate (thion-DPPA) and zwitterion, i.e. 1,2-dipalmitoyl-rac-3-phosphocholine and 1,2-distearoyl-rac-glycero-3-phosphocholine (DPPC and DSPC), lipids has been investigated. The phase transition was detected using the jump-like increase effect in the conductance of the planar bilayer membrane. A voltage increase to 150 mV has been shown to increase the phase transition temperature in a bilayer lipid membrane (BLM) of phosphatidic acids (DPPA and thion-DPPA) by 8-12 degrees C while the transition temperature in the bilayer of zwitterion lipids (DPPC and DSPC) increases insignificantly. The increasing of Tt in BLM of acidic lipids is attributed to the voltage-induced changes in the molecule packing density.

Chemical Phenomena↗
PubMedDate not supplied

Lipid-phase transition of phosphatidylglycerol in Acholeplasma laidlawii membranes studied with phospholipase A2.

Phospholipase A2 was applied to follow the lipid phase transition of phosphatidylglycerol in the membrane of Acholeplasma laidlawii. The conclusions were identical with those obtained with physicochemical techniques. In addition, it was shown that phosphatidylglycerol undergoes the lipid phase transition in the same temperature range as the bulk of the membrane lipid; phase segregation between various molecular species of phosphatidylglycerol occurs; exchange of this phospholipid between rigid and fluid domains is a slow, temperature-dependent process; and phosphatidylglycerol-protein interactions do occur at temperatures above that of the lipid phase transition.

Acholeplasma laidlawii↗
PubMed2001

Phase transitions and molecular motion in the cell.

The cytoplasm exhibits all of the signature characteristics of a gel. The thesis put forth here is that the cytoplasm's gel-like character is central to the generation of biological movement. In artificial gels, a common vehicle for generating movement is the polymer-gel phase-transition. By undergoing phase-transition, gels produce motion of both solvent and solutes. It is argued that cells do the same. Three examples are given: the secretory system, the muscle contraction system and the biological streaming system. In each case it is shown that the characteristic motions may be created as proteins and water undergo transition from an expanded, hydrated state to a contracted, dehydrated state--or the reverse. These changes shift solutes and solvent in a characteristic way that depends on the respective organelle's structure. Phase-transitions are simple, powerful mechanisms that may be responsible for many, if not all, biological motions.

Actins↗