Spin-labeled Phospholipids Research Articles

Measuring local pH at interfaces from molecular tumbling: A concept for designing EPR-active pH-sensitive labels and probes.

Molecular probes and indicators are broadly employed for pH measurements in bulk media and at interfaces. The underlying physical principle of pH measurements of most of these probes is based on a change in the electronic structure that, for example, results in a shift of the emission peak of the fluorescence probes, changes in NMR chemical shifts due to the affected electronic shielding, or magnetic parameters of pH-sensitive nitroxides as measured by EPR. Here we explore another concept for measuring local protonation state of molecular tags based on changes in rotational dynamics of electron spin-bearing moieties that are readily detected by conventional continuous wave X-band EPR. Such changes are especially pronounced at biological interfaces, such as lipid bilayer membranes, due to the probe interactions with adjacent charges and polarizable dipoles. The concept was demonstrated by synthesizing a series of pH-sensitive nitroxides and spin-labelled phospholipids. EPR spectra of these newly synthesized nitroxides exhibit relatively small - about 0.5 G - changes in isotropic nitrogen hyperfine coupling constant upon reversible protonation. However, spin-labelled phospholipids incorporated into lipid bilayers demonstrated almost 6-fold change in rotational correlation time upon protonation, readily allowing for pKa determination from large changes in EPR spectra. The demonstrated concept of EPR-based pH measurements leads to a broader range of potential nitroxide structures that can serve as molecular pH sensors at the desired pH range and, thus, facilitates further development of spin-labelling EPR methods to study electrostatic phenomena at chemical and biological interfaces.

Fluorescence Studies of Nicotinic Acetylcholine Receptor and Its Associated Lipid Milieu: The Influence of Erwin London's Methodological Approaches.

Erwin London dedicated considerable effort to understanding lipid interactions with membrane-resident proteins and how these interactions shaped the formation and maintenance of lipid phases and domains. In this endeavor, he developed ad hoc techniques that greatly contributed to advancements in the field. We have employed and/or modified/extended some of his methodological approaches and applied them to investigate lipid interaction with the nicotinic acetylcholine receptor (nAChR) protein, the paradigm member of the superfamily of rapid pentameric ligand-gated ion channels (pLGIC). Our experimental systems ranged from purified receptor protein reconstituted into synthetic lipid membranes having known effects on receptor function, to cellular systems subjected to modification of their lipid content, e.g., varying cholesterol levels. We have often employed fluorescence techniques, including fluorescence quenching of diphenylhexatriene (DPH) extrinsic fluorescence and of nAChR intrinsic fluorescence by nitroxide spin-labeled phospholipids, DPH anisotropy, excimer formation of pyrene-phosphatidylcholine, and Förster resonance energy transfer (FRET) from the protein moiety to the extrinsic probes Laurdan, DPH, or pyrene-phospholipid to characterize various biophysical properties of lipid-receptor interactions. Some of these strategies are revisited in this review. Special attention is devoted to the anionic phospholipid phosphatidic acid (PA), which stabilizes the functional resting form of the nAChR. The receptor protein was shown to organize its PA-containing immediate microenvironment into microdomains with high lateral packing density and rigidity. PA and cholesterol appear to compete for the same binding sites on the nAChR protein.

ESR Spectroscopy Determines the Affinity of Cholesterol for Lipids with Varying Degrees of Unsaturation

Membrane organization and the formation of lipid rafts have been studied extensively to provide a better understanding of cellular signaling and function. Previous studies have shown that cell and model membranes segregate into raft-like domains, regions rich in cholesterol and saturated lipids that play a role in membrane signaling, and cholesterol-poor regions, rich in unsaturated lipids. Cholesterol, an abundant lipid in mammalian cell membranes, orders lipid motion and has an aversion for the disordered acyl chains of polyunsaturated phospholipids, thus, cholesterol-lipid interactions are thought to play a key role in promoting lateral segregation in membranes. Here we present a new method for measuring the relative affinity of cholesterol between different lipids using electron spin resonance (ESR) spectroscopy and a phospholipid spin-label, 1-palmitoyl-2-stearoyl-(5-doxyl)-sn-glycero-3-phosphocholine (P(5DSA)PC). Using this technique, we measure the partitioning of cholesterol between large unilamellar vesicles (LUVs) of 1-palmitoyl-2-oleyol-phosphatidylcholine (POPC), our reference, and LUVs composed of lipids with varying degrees of unsaturation. These partitioning experiment results will be reported, as well as preliminary experiments showing the first, to our knowledge, partitioning experiments for vitamin E.

Ether-linked lipids: Spin-label EPR and spin echoes

Electron spin echo envelope modulation (ESEEM) and conventional electron paramagnetic resonance (EPR) of site-specifically spin-labelled phospholipids are used to investigate the effect of ether-linked chains on the water-penetration and polarity profiles, as well as the phase behaviour and chain flexibility profiles, of phospholipid membranes. D2O-ESEEM reveals that water exposure of the terminal methyl groups in the interdigitated phase of dihexadecyl phosphatidylcholine (DHPC) is comparable to that of the methylene groups at the polar head-group end of the chains. Similarly, an uniform transmembrane polarity profile is obtained from the dependence of the outer 14N-hyperfine splitting on the spin-label position along the chain in frozen interdigitated DHPC dispersions. Two-component conventional EPR spectra of spin labels at the terminal methyl end of the chain reveal that the intermediate gel phase above the pretransition of DHPC contains components in which the lipid chains are interdigitated. The polarity and chain-flexibility profiles in the fluid Lα-phase of DHPC with ether-linked chains are shifted outwards, towards the polar-apolar interface, as compared with that of dihexadecanoyl phosphatidylcholine (DPPC) with ester-linked chains. Also, the polarity profile of DHPC is shifted upwards, to higher polarities. These differences reflect those in hydrocarbon thickness and area/lipid molecule reported by x-ray diffraction for the Lα-phases of the two lipids.

EPR and fluorescence study of molecular dynamics of lipids in bilayers adsorbed on porous silica gel

Lipid bilayers immobilized on highly porous silica gel monoliths (SLBs) have been proposed as templates for chemosensors. Procedures for preparation and characterization of SLBs have been developed and applied. Rotational dynamics and orientational ordering at different depths in a SLB membrane and, for comparison, in bilayer liposomes have been studied for the first time using n-PC phospholipid spin labels.

Ionizable Nitroxides for Studying Local Electrostatic Properties of Lipid Bilayers and Protein Systems by EPR.

Electrostatic interactions are known to play a major role in the myriad of biochemical and biophysical processes. Here, we describe biophysical methods to probe local electrostatic potentials of proteins and lipid bilayer systems that are based on an observation of reversible protonation of nitroxides by electron paramagnetic resonance (EPR). Two types of probes are described: (1) methanethiosulfonate derivatives of protonatable nitroxides for highly specific covalent modification of the cysteine's sulfhydryl groups and (2) spin-labeled phospholipids with a protonatable nitroxide tethered to the polar head group. The probes of both types report on their ionization state through changes in magnetic parameters and degree of rotational averaging, thus, allowing the electrostatic contribution to the interfacial pKa of the nitroxide, and, therefore, the local electrostatic potential to be determined. Due to their small molecular volume, these probes cause a minimal perturbation to the protein or lipid system. Covalent attachment secures the position of the reporter nitroxides. Experimental procedures to characterize and calibrate these probes by EPR, and also the methods to analyze the EPR spectra by simulations are outlined. The ionizable nitroxide labels and the nitroxide-labeled phospholipids described so far cover an exceptionally wide range of ca. 2.5-7.0 pH units, making them suitable to study a broad range of biophysical phenomena, especially at the negatively charged lipid bilayer surfaces. The rationale for selecting proper electrostatically neutral interface for probe calibration, and examples of lipid bilayer surface potential studies, are also described.

Omega-3 Fatty Acids Regulate the Interaction of the Alzheimer’s Aβ(25–35) Peptide with Lipid Membranes

Polyunsaturated omega-3 fatty acids are increasingly proposed as dietary supplements able to reduce the risk of development or progression of the Alzheimer's disease (AD). To date, the molecular mechanism through which these lipids act has not been yet univocally identified. In this work, we investigate whether omega-3 fatty acids could interfere with the fate of the Alzheimer-related amyloid peptide by tuning the microstructural and dynamical properties of the neuronal membrane. To this aim, the influence of the omega-3 lipid, 1,2-didocosahexaenoyl-sn-glycero-3-phosphocholine [22:6(cis)PC] on the biophysical properties of lipid bilayers, and on their interaction with the amyloid peptide fragment Aβ(25-35) has been investigated by Electron Spin Resonance (ESR), using spin-labeled phospholipids. The results show that the peptide selectively interacts with bilayers enriched in cholesterol (Chol) and sphingomyelin (SM). [22:6(cis)PC] enhances the Aβ(25-35)/membrane interaction, favoring a deeper internalization of the peptide among the lipid acyl chains and, consequently, hindering its pathogenic self-aggregation.

Molecular Dynamics Simulations of Depth Distribution of Spin-Labeled Phospholipids within Lipid Bilayer

Spin-labeled lipids are commonly used as fluorescence quenchers in studies of membrane penetration of dye-labeled proteins and peptides using depth-dependent quenching. Accurate calculations of depth of the fluorophore rely on the use of several spin labels placed in the membrane at various positions. The depth of the quenchers (spin probes) has to be determined independently; however, experimental determination of transverse distributions of spin probe depths is difficult. In this Article, we use molecular dynamics (MD) simulations to study the membrane behavior and depth distributions of spin-labeled phospholipids in a 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) bilayer. To probe different depths within the bilayer, a series containing five Doxyl-labeled lipids (n-Doxyl PC) has been studied, in which a spin moiety was covalently attached to nth carbon atoms (where n = 5, 7, 10, 12, and 14) of the sn-2 stearoyl chain of the host phospholipid. Our results demonstrate that the chain-attached spin labels are broadly distributed across the model membrane and their environment is characterized by a high degree of mobility and structural heterogeneity. Despite the high thermal disorder, the depth distributions of the Doxyl labels were found to correlate well with their attachment positions, indicating that the distribution of the spin label within the model membrane is dictated by the depth of the nth lipid carbon atom and not by intrinsic properties of the label. In contrast, a much broader and heterogeneous distribution was observed for a headgroup-attached Tempo spin label of Tempo-PC lipids. MD simulations reveal that, due to the hydrophobic nature, a Tempo moiety favors partitioning from the headgroup region deeper into the membrane. Depending on the concentration of Tempo-PC lipids, the probable depth of the Tempo moiety could span a range from 14.4 to 18.2 Å from the membrane center. Comparison of the MD-estimated immersion depths of Tempo and n-Doxyl labels with their suggested experimental depth positions allows us to review critically the possible sources of error in depth-dependent fluorescence quenching studies.

Effects of Lipid Structure on the State of Aggregation of Potassium Channel KcsA

The state of aggregation of potassium channel KcsA was determined as a function of lipid:protein molar ratio in bilayer membranes of the zwitterionic lipid phosphatidylcholine (PC) and of the anionic lipid phosphatidylglycerol (PG). EPR (electron paramagnetic resonance) with spin-labeled phospholipids was used to determine the number of motionally restricted lipids per KcsA tetramer. Unexpectedly, this number decreased with a decreasing lipid:KcsA tetramer molar ratio in the range of 88:1 to 30:1, consistent with sharing of annular lipid shells and KcsA-KcsA contact at high mole fractions of protein. Fluorescence quenching experiments with brominated phospholipids showed a decrease in fluorescence quenching at low lipid:KcsA tetramer mole ratios, also consistent with KcsA-KcsA contact at high mole fractions of protein. The effects of low mole ratios of lipid seen in EPR and fluorescence quenching experiments were more marked in bilayers of PC than in bilayers of PG, suggesting stronger association of PG than PC with KcsA. This was confirmed by direct measurement of lipid association constants using spin-labeled phospholipids, showing higher association constants for all anionic lipids than for PC. The results show that the probability of contacts between KcsA tetramers will be very low at lipid:protein molar ratios that are typical of native biological membranes.

Phase Diagram of Ternary Cholesterol/Palmitoylsphingomyelin/Palmitoyloleoyl-Phosphatidylcholine Mixtures: Spin-Label EPR Study of Lipid-Raft Formation

For canonical lipid raft mixtures of cholesterol (chol), N-palmitoylsphingomyelin (PSM), and 1-palmitoyl-2-oleoylphosphatidylcholine (POPC), electron paramagnetic resonance (EPR) of spin-labeled phospholipids—which is insensitive to domain size—is used to determine the ternary phase diagram at 23°C. No phase boundaries are found for binary POPC/chol mixtures, nor for ternary mixtures with PSM content <24 mol %. EPR lineshapes indicate that conversion from the liquid-disordered (Lα) to liquid-ordered (Lo) phase occurs continuously in this region. Two-component EPR spectra and several tie lines attributable to coexistence of gel (Lβ) and fluid phases are found for ternary mixtures with low cholesterol or low POPC content. For PSM/POPC alone, coexistence of Lα and Lβ phases occurs over the range 50−95.5 mol % PSM. A further tie line is found at 3 mol % chol with endpoints at 50 and ≥77 mol % PSM. For PSM/chol, Lβ−Lo coexistence occurs over the range 10−38 mol % chol and further tie lines are found at 4.5 and 7 mol % POPC. Two-component EPR spectra indicative of fluid-fluid (Lα−Lo) phase separation are found for lipid compositions: 25%<PSM<65%, 5%<chol<30–35%, 65%>POPC>10%, and confirmed by nonlinear EPR. Tie lines are identified in the Lα−Lo coexistence region, indicating that the fluid domains are of sufficient size to obey the phase rule. The three-phase triangle is bounded approximately by the compositions 40 and 75 mol % PSM with 10 mol % chol, and 60 mol % PSM with 25 mol % chol. These studies define the compositions of raft-like Lo phases for a minimal realistic biological lipid mixture.

Organization and Dynamics of Hippocampal Membranes in a Depth-Dependent Manner: An Electron Spin Resonance Study

Organization and dynamics of neuronal membranes represent crucial determinants for the function of neuronal receptors and signal transduction. Previous work from our laboratory has established hippocampal membranes as a convenient natural source for studying neuronal receptors. In this work, we have monitored the organization and dynamics of hippocampal membranes and their modulation by cholesterol and protein content utilizing location (depth)-specific spin-labeled phospholipids by ESR spectroscopy. The choice of ESR spectroscopy is appropriate due to slow diffusion encountered in crowded environments of neuronal membranes. Analysis of ESR spectra shows that cholesterol increases hippocampal membrane order while membrane proteins increase lipid dynamics resulting in disordered membranes. These results are relevant in understanding the complex organization and dynamics of hippocampal membranes. Our results are significant in the overall context of membrane organization under low cholesterol conditions and could have implications in neuronal diseases characterized by low cholesterol conditions due to defective cholesterol metabolism.

Phase Boundaries in Phosphatidylcholine Membranes Saturated and Oversaturated with Cholesterol

Conventional and saturation-recovery EPR along with differential scanning calorimetry (DSC) were used to determine the cholesterol/phosphatidylcholine (Chol/PC) mixing ratio at which cholesterol bilayer domains (CBDs) and cholesterol crystals (CR) start to form in dimyristoyl-PC (DMPC) and 1-palmitoyl-2-oleoy-PC (POPC) membranes. The Chol/PC mixing ratio was changed from 0 to 3. Lipid multilamellar dispersions investigated in this work were prepared using the rapid solvent exchange method to preserve compositional homogeneity throughout the suspension. EPR spin-labeling methods were used with spin-labeled cholesterol analogues (cholestane spin label [CSL] and androstane spin label [ASL]) as well as with a spin-labeled phospholipid (1-palmitoyl-2-(5-doxylstearoyl)phosphatidylcholine (5-PC)) to locate the phase boundary for CBD formation. DSC was used to locate the phase boundary for the formation of CRs. Results showed that in both DMPC and POPC membranes the CBD is already formed at a Chol/PC mixing ratio of 1, while CRs are formed only when the Chol/PC mixing ratio exceeds the value of 2. Previous results and data presented here indicate that when the Chol/PC mixing ratio increases, the PC bilayer becomes saturated with cholesterol first. This phospholipid bilayer, saturated with cholesterol, possesses unique physical properties. Increase in cholesterol content beyond the Chol/PC mixing ratio of 1 causes formation of the CBD, and further increase, beyond the Chol/PC mixing ratio of 2, causes formation of CRs (presumably outside of the membrane). Thus, the phase boundary at a Chol/PC mixing ratio of 1 separates the region with a single liquid-ordered phase and the region with a coexisting liquid-ordered phase and CBD. The cholesterol solubility threshold at a Chol/PC mixing ratio of 2 separates the region with a coexisting liquid-ordered phase and CBD from the region in which CRs are formed.

Membrane Fluidity Profiles as Deduced by Saturation-Recovery EPR Measurements of Spin-Lattice Relaxation Times of Spin Labels: Multifrequency Approach

New capabilities using saturation-recovery (SR) EPR at X-band (9.4 GHz) and W-band (94 GHz) to obtain profiles of the membrane fluidity have been demonstrated for dimyristoylphosphatidylcholine (DMPC) membranes with and without 50 mol% cholesterol. Phosphatidylcholine (n-PC) spin labels were used. Results were compared with profiles of the rotational diffusion coefficient, Rperp, obtained from simulation of EPR spectra using Freed's model. The spin-lattice relaxation rate (T1−1) obtained from SR EPR measurements of phospholipid spin labels in deoxygenated samples depends primarily on the rotational correlation time of the nitroxide moiety within the lipid bilayer. Thus, T1−1 can be used as a convenient quantitative measure of membrane fluidity that reflects membrane dynamics at a certain depth in the membrane. The order parameter, which is often used as a measure of membrane fluidity, describes the amplitude of wobbling motion of alkyl chains relative to the membrane normal and does not explicitly contain time or velocity. Thus, the order parameter can be considered as “nondynamic”. It is shown that T1−1 and Rperp profiles reveal changes in membrane fluidity that depend on the motional properties of the lipid alkyl chain. We find that cholesterol has a rigidifying effect only to the depth occupied by the rigid steroid ring structure and a fluidizing effect at deeper locations. These effects cannot be differentiated by profiles of the order parameter. Results demonstrate that SR EPR at W-band has the potential to be a powerful tool for studying samples of small volume, ∼30 nL, compared with a sample volume of ∼3 μL typically required at X-band.

Two Conserved Residues Are Important for Inducing Highly Ordered Membrane Domains by the Transmembrane Domain of Influenza Hemagglutinin

The interaction with lipids of a synthetic peptide corresponding to the transmembrane domain of influenza hemagglutinin was investigated by means of electron spin resonance. A detailed analysis of the electron spin resonance spectra from spin-labeled phospholipids revealed that the major effect of the peptide on the dynamic membrane structure is to induce highly ordered membrane domains that are associated with electrostatic interactions between the peptide and negatively charged lipids. Two highly conserved residues in the peptide were identified as being important for the membrane ordering effect. Aggregation of large unilamellar vesicles induced by the peptide was also found to be correlated with the membrane ordering effect of the peptide, indicating that an increase in membrane ordering, i.e., membrane dehydration, is important for vesicle aggregation. The possibility that hydrophobic interaction between the highly ordered membrane domains plays a role in vesicle aggregation and viral fusion is discussed.

Self-organization and phase structure of ternary lipid membranes: A spin label EPR study

The phase structure of membranes formed by ternary lipid mixtures, palmitoyl sphingomyelin (PSM)/palmitoyl oleoyl phosphatidylcholine (POPC)/Cholesterol (Chol), the composition of which simulates that of cell membranes, was studied by EPR using spin-labeled phospholipids. It is shown that, in the two-component POPC/Chol membranes and ternary membranes with a low (less than 24%) fraction of PSM, no phase boundaries are observed and the transition from the liquid disordered (ld) phase to the liquid ordered (lo) phase occurs continuously. In contrast, two-component EPR spectra and tie lines are detected in the other two-component systems, PSM/POPC and PSM/Chol, as well as in the ternary systems with a low content of Chol or POPC, respectively. These features are indicative of the coexistence of the gel phase (Lβ) and two liquid phases, ld or lo, respectively. The tie lines are approximately parallel to the Gibbs triangle sides Chol = 0 and POPC = 0, respectively. In the central part of the Gibbs triangle, where a sufficiently fast rotational diffusion of the spin labels indicates the membrane liquid state, we also observed two-component EPR spectra with quite different magnetic anisotropy and tie lines, indicating the coexistence of ld and lo phases. The boundaries are found for all the two-phase coexistence regions. The localization of the three-phase (Lβ, ld, and lo) coexistence region between the two-phase regions (Lβ-ld, Lβ-lo, and ld-lo) was proposed on the basis of an EPR-line shape analysis.

A Flippase-Independent Function of Atp8b1, the Protein Affected in Familial Intrahepatic Cholestasis Type 1, Is Required for Apical Protein Expression and Microvillus Formation in Polarized Epithelial Cells

Mutations in ATP8B1 cause familial intrahepatic cholestasis type 1, a spectrum of disorders characterized by intrahepatic cholestasis, reduced growth, deafness, and diarrhea. ATP8B1 belongs to the P(4) P-type adenosine triphosphatase (ATPase) family of putative aminophospholipid translocases, and loss of aminophospholipid asymmetry in the canalicular membranes of ATP8B1-deficient liver cells has been proposed as the primary cause of impaired bile salt excretion. To explore the origin of the hepatic and extrahepatic symptoms associated with ATP8B1 deficiency, we investigated the impact of ATP8B1 depletion on the domain-specific aminophospholipid translocase activities and polarized organization of polarized epithelial Caco-2 cells. Caco-2 cells were stably transfected with short hairpin RNA constructs to block ATP8B1 expression. Aminophospholipid translocase activity was assessed using spin-labeled phospholipids. The polarized organization of these cells was determined by pulse-chase analysis, cell-fractionation, immunocytochemistry, and transmission electron microscopy. ATP8B1 was abundantly expressed in the apical membrane of Caco-2 cells, and its expression was markedly induced during differentiation and polarization. Blocking ATP8B1 expression by RNA interference (RNAi) affected neither aminophospholipid transport nor the asymmetrical distribution of aminophospholipids across the apical bilayer. Nonetheless, ATP8B1-depleted Caco-2 cells displayed profound perturbations in apical membrane organization, including a disorganized apical actin cytoskeleton, a loss in microvilli, and a posttranscriptional defect in apical protein expression. Our findings point to a critical role of ATP8B1 in apical membrane organization that is unrelated to its presumed aminophospholipid translocase activity, yet potentially relevant for the development of cholestasis and the manifestation of extrahepatic features associated with ATP8B1 deficiency.

Surface Electrostatics and Lipid-Substrate Interactions of Nanopore-Confined Lipid Bilayers

Substrate-supported lipid bilayers serve many purposes: from acting as versatile models of cellular membranes to biotechnological applications including substrate functionalization and stabilizing membrane proteins in functional conformations. While adsorption and subsequent reorganization of phospholipid vesicles on solid substrates were studied in the past, the exact nature of physicochemical interactions between the lipids and substrate surfaces remain largely unknown. Here we employed recently synthesized pH-sensitive spin-labeled phospholipids - derivatives of 1,2-dipalmitoyl-sn-glycero-3-phosphothioethanol (PTE) with pH-reporting nitroxides that are covalently attached to the lipid's headgroup - to investigate surface electrostatics of nanotubular lipid bilayers confined in cylindrical nanopores. The lipid nanotubes were formed by self-assembling phospholipids inside ordered nanochannels of anodic aluminum oxide with pore diameters from 60 to 170 nm and diameter-to-pore length ratio of up to 1:1000. 31P NMR confirmed formation of macroscopically aligned lipid nanotubes with just 1-2° mosaic spread from zwitterionic DMPC, anionic DMPG, and their mixtures. Interfacial potentials were measured by carrying out titration experiments and observing the protonation state of the nitroxide tag by EPR. For nanopore-confined DMPC:DMPG (1:1) bilayers the protonation equilibrium was shifted to more acidic values: when the single lipid bilayer was deposited per nanopore the pKa of the nitroxide probe was shifted by (−0.91±0.05) pH units but only by (−0.34±0.05) when three bilayers per nanopore were present. Notably, the nitrogen hyperfine coupling constant for non-protonated nitroxides remained the same in all the samples indicating essentially the same interfacial dielectric environment. Thus, these shifts in pKa must come from changes in the lipid bialyer surface potential that was estimated to increase by 52±3 mV. EPR data on the lipid-substrate interface were combined with differential scanning calorimetry to elucidate effects of pore curvature, surface modification, and binding of antibacterial peptides on lipid-substrate interactions. Supported by DE-FG02-02ER15354.

Segregated Phases in Pulmonary Surfactant Membranes Do Not Show Coexistence of Lipid Populations with Differentiated Dynamic Properties

The composition of pulmonary surfactant membranes and films has evolved to support a complex lateral structure, including segregation of ordered/disordered phases maintained up to physiological temperatures. In this study, we have analyzed the temperature-dependent dynamic properties of native surfactant membranes and membranes reconstituted from two surfactant hydrophobic fractions (i.e., all the lipids plus the hydrophobic proteins SP-B and SP-C, or only the total lipid fraction). These preparations show micrometer-sized fluid ordered/disordered phase coexistence, associated with a broad endothermic transition ending close to 37°C. However, both types of membrane exhibit uniform lipid mobility when analyzed by electron paramagnetic resonance with different spin-labeled phospholipids. A similar feature is observed with pulse-field gradient NMR experiments on oriented membranes reconstituted from the two types of surfactant hydrophobic extract. These latter results suggest that lipid dynamics are similar in the coexisting fluid phases observed by fluorescence microscopy. Additionally, it is found that surfactant proteins significantly reduce the average intramolecular lipid mobility and translational diffusion of phospholipids in the membranes, and that removal of cholesterol has a profound impact on both the lateral structure and dynamics of surfactant lipid membranes. We believe that the particular lipid composition of surfactant imposes a highly dynamic framework on the membrane structure, as well as maintains a lateral organization that is poised at the edge of critical transitions occurring under physiological conditions.

Structural properties of lipid reconstructs and lipid composition of normotensive and hypertensive rat vascular smooth muscle cell membranes

Multiple cell membrane alterations have been reported to be the cause of various forms of hypertension. The present study focuses on the lipid portion of the membranes, characterizing the microviscosity of membranes reconstituted with lipids extracted from the aorta and mesenteric arteries of spontaneously hypertensive (SHR) and normotensive control rat strains (WKY and NWR). Membrane-incorporated phospholipid spin labels were used to monitor the bilayer structure at different depths. The packing of lipids extracted from both aorta and mesenteric arteries of normotensive and hypertensive rats was similar. Lipid extract analysis showed similar phospholipid composition for all membranes. However, cholesterol content was lower in SHR arteries than in normotensive animal arteries. These findings contrast with the fact that the SHR aorta is hyporeactive while the SHR mesenteric artery is hyperreactive to vasopressor agents when compared to the vessels of normotensive animal strains. Hence, factors other than microviscosity of bulk lipids contribute to the vascular smooth muscle reactivity and hypertension of SHR. The excess cholesterol in the arteries of normotensive animal strains apparently is not dissolved in bulk lipids and is not directly related to vascular reactivity since it is present in both the aorta and mesenteric arteries. The lower cholesterol concentrations in SHR arteries may in fact result from metabolic differences due to the hypertensive state or to genes that co-segregate with those that determine hypertension during the process of strain selection.

The interaction of neuropeptide Y with negatively charged and zwitterionic phospholipid membranes

The interaction of the 36 amino acid neuropeptide Y (NPY) with liposomes was studied using the intrinsic tyrosine fluorescence of NPY and an NPY fragment comprising amino acids 18-36. The vesicular membranes were composed of phosphatidylcholine and phosphatidylserine at varying mixing ratios. From the experimentally measured binding curves, the standard Gibbs free energy for the peptide transfer from aqueous solution to the lipid membrane was calculated to be around -30 kJ/mol for membrane mixtures containing physiological amounts of acidic lipids at pH 5. The effective charge of the peptide depends on the pH of the buffer and is about half of its theoretical net charge. The results were confirmed using the fluorescence of the NPY analogue [Trp(32)]-NPY. Further, the position of NPY's alpha-helix in the membrane was estimated from the intrinsic tyrosine fluorescence of NPY, from quenching experiments with spin-labelled phospholipids using [Trp(32)]-NPY, and from (1)H magic-angle spinning NMR relaxation measurements using spin-labelled [Ala(31), TOAC(32)]-NPY. The results suggest that the immersion depth of NPY into the membrane is triggered by the membrane composition. The alpha-helix of NPY is located in the upper chain region of zwitterionic membranes but its position is shifted to the glycerol region in negatively charged membranes. For membranes composed of phosphatidylcholine and phosphatidylserine, an intermediate position of the alpha-helix is observed.