Pyrenedodecanoic Acid Research Articles

Par j 1 and Par j 2, the two major allergens in Parietaria judaica, bind preferentially to monoacylated negative lipids

Par j 1 and Par j 2 proteins are the two major allergens in Parietaria judaica pollen, one of the main causes of allergic diseases in the Mediterranean area. Each of them contains eight cysteine residues organized in a pattern identical to that found in plant nonspecific lipid transfer proteins. The 139- and 102-residue recombinant allergens, corresponding respectively to Par j 1 and Par j 2, refold properly to fully functional forms, whose immunological properties resemble those of the molecules purified from the natural source. Molecular modeling shows that, despite the lack of extensive primary structure homology with nonspecific lipid transfer proteins, both allergens contain a hydrophobic cavity suited to accommodate a lipid ligand. In the present study, we present novel evidence for the formation of complexes of these natural and recombinant proteins from Parietaria pollen with lipidic molecules. The dissociation constant of oleyl-lyso-phosphatidylcholine is 9.1 +/- 1.2 microm for recombinant Par j 1, whereas pyrenedodecanoic acid shows a much higher affinity, with a dissociation constant of approximately 1 microm for both recombinant proteins, as well as for the natural mixture. Lipid binding does not alter the secondary structure content of the protein but is very efficient in protecting disulfide bonds from reduction by dithiothreitol. We show that Par j 1 and Par j 2 not only bind lipids from micellar dispersions, but also are able to extract and transfer negative phospholipids from bilayers.

P2-064: Long-term cognitive and behavioral response, and liquid crystalline states of brain mitochondrial membrane in estrogen-treated mice exposed to low-dose radiation in utero

Estrogen has been recently shown to play a neuroprotective role apart from popular view of its functions in human reproduction. In our research, we focused on the long–term membrane effects of estrogen on brain mitochondria and correlated these findings with its beneficial effects on cognitive and behavioral skills. Using an in utero radiation model of mice, the liquid crystalline (LC) organization of mitochondrial membrane from 60–day old mice was investigated by analyzing the self–organized LC textures, thermotropic transitions, and measured its lateral mobility. Various behavioral and cognitive tests were done. The organization of brain mitochondrial membranes of adult mice irradiated in utero at 17 dpc exhibited a decrease in unit texture size from 11.2–16.68 μm in control mouse to 5.58–11.12 μm in 1.0 and 1.5 Gy–irradiated mice. The ability of lyotropic LC domains to undergo intermediary phase changes and aggregate into more complex structures, e.g. coarse mosaic and pseudoisotropic textures, was ablated in the fetally–irradiated mice and this was not reversed even with post–natal treatment of 25 μg estradiol s.c. on day 5. Interestingly, estradiol treatment increased mitochondrial membrane fluidity in irradiated mice based on the calculated lateral diffusion coefficients from the quantum ratio, I' (excimer intensity)/I (monomer intensity) with 1–pyrene dodecanoic acid as probe. The effects of estradiol on lateral diffusion are not dependent on the radiation dose used and the sex. The biophysical data is consistent with the cognitive skills and behavioral patterns of the mice. Our results provide new insights on the molecular mechanisms of how estrogen acts in dampening neurodegeneration from a concurrent biophysical and behavioral perspective.

Effect of gramicidin addition upon the physicochemical properties of dipalmitoyl phosphatidyl choline large unilamellar vesicles

In this work, we report the results bearing on the effect of gramicidin incorporation upon the dynamic and structural properties of dipalmitoyl phosphatidyl choline (DPPC) large unilamellar vesicle (LUVs). Results were obtained at different depths in the bilayer, both in the bulk of the bilayer and the vicinity of the added pentadecapeptide. This analysis was performed employing a series of extrinsic fluorescent probes (1,6-diphenyl-1,3,5-hexatriene (DPH), 1-(4-trimethylammonium phenyl)-6-phenyl-1,3,5-hexatriene (TMA-DPH), 6-dodecanoyl-2-dimethyl aminenaphthalene (Laurdan), pyrenedodecanoic acid, pyrene butyric acid, 1-hexadecanoyl-2-(1-pyrenedecanoyl)-sn-glycero-3-phosphocholine (Py–C 10–PC) and 1,2-bis-(1-pyrenedecanoyl)-sn-glycero-3-phosphocholine (bis-Py–C 10–PC)). Fluorescence measurements were carried out after direct excitation of the probe or after its excitation by resonant energy transfer (RET) from the intrinsic tryptophan groups of the polypeptide. The last procedure allows an evaluation of the lipidic annulus properties in the vicinity of the incorporated polypeptide. In the gel state, gramicidin incorporation increases the order near the vesicle interface, as sensed by TMA-DPH. This increase is observed, above the phase transition temperature, over all the bilayer. This effect is probably related to a decrease in the lateral diffusion of the lipids, as evidenced by the reduced formation of intermolecular excimers following Py–C 10–PC excitation. Gramicidin incorporation also increases the penetration and/or mobility of water molecules located near the bilayer interface. In the gel phase, these changes are more relevant in the central part of the bilayer. When the LUVs are in the liquid crystalline state, the effect is observed through all the bilayer. In this state, the polypeptide incorporation also increases the diffusion/concentration of oxygen, irrespective of the probe localization. Resonance energy transfer between Trp residues and Laurdan, Py–C 10–PC or bis-Py–C 10–PC dyes was employed to evaluate the properties of the lipidic annulus surrounding the polypeptide. In the gel phase, gramicidin incorporation produces an increase in the penetration and/or dynamics of water molecules, while in the liquid crystalline state it leads to a decrease of the acyl chain mobility in the deepest parts of the bilayer.

Aggregation behaviour of hydrophobically modified poly(allylammonium) chloride

The behaviour of hydrophobically modified poly(allylammonium) chloride having octyl, decyl, dodecyl and hexadecyl side chains has been studied in aqueous solution using fluorescence emission techniques. Micropolarity studies using the I 1/I 3 ratio of the vibronic bands of pyrene show that the formation of hydrophobic microdomains depends on both the length of the side chain and the polymer concentration. The I 1/I 3 ratio of the polymers with low hydrophobe content (less than 5% mol) changes substantially when reaching a certain concentration. These changes are assigned to aggregation originating from interchain interactions. This behaviour is also confirmed by the behaviour of the monomer/excimer emission intensities of pyrenedodecanoic acid used as a probe. For polymers having dodecyl side chains and hydrophobe contents higher than 10%, aggregates are formed independently of the polymer concentration. Anisotropy measurements show that microdomains resulting from the inter- and/or intramolecular interactions are similar to those observed for cationic surfactants. Viscosity measurements show that the coil dimensions are substantially decreased for the polymers having high hydrophobe contents, indicating intramolecular associations.

High-affinity binding of very-long-chain fatty acyl-CoA esters to the peroxisomal non-specific lipid-transfer protein (sterol carrier protein-2)

Binding of fluorescent fatty acids to bovine liver non-specific lipid-transfer protein (nsL-TP) was assessed by measuring fluorescence resonance energy transfer (FRET) between the single tryptophan residue of nsL-TP and the fluorophore. Upon addition of pyrene dodecanoic acid (Pyr-C12) and cis-parinaric acid to nsL-TP, FRET was observed indicating that these fatty acids were accommodated in the lipid binding site closely positioned to the tryptophan residue. Substantial binding was observed only when these fatty acids were presented in the monomeric form complexed to β-cyclodextrin. As shown by time-resolved fluorescence measurements, translocation of Pyr-C12 from the Pyr-C12–β-cyclodextrin complex to nsL-TP changed dramatically the direct molecular environment of the pyrene moiety: i.e. the fluorescence lifetime of the directly excited pyrene increased at least by 25% and a distinct rotational correlation time of 7 ns was observed. In order to evaluate the affinity of nsL-TP for intermediates of the β-oxidation pathway, a binding assay was developed based on the ability of fatty acyl derivatives to displace Pyr-C12 from the lipid binding site as reflected by the reduction of FRET. Hexadecanoyl-CoA and 2-hexadecenoyl-CoA were found to bind readily to nsL-TP, whereas 3-hydroxyhexadecanoyl-CoA and 3-ketohexadecanoyl-CoA bound poorly. The highest affinities were observed for the very-long-chain fatty acyl-CoA esters (24:0-CoA, 26:0-CoA) and their enoyl derivatives (24:1-CoA, 26:1-CoA). Binding of non-esterified hexadecanoic acid and tetracosanoic acid (24:0) was negligible.

High-affinity binding of very-long-chain fatty acyl-CoA esters to the peroxisomal non-specific lipid-transfer protein (sterol carrier protein-2)

Binding of fluorescent fatty acids to bovine liver non-specific lipid-transfer protein (nsL-TP) was assessed by measuring fluorescence resonance energy transfer (FRET) between the single tryptophan residue of nsL-TP and the fluorophore. Upon addition of pyrene dodecanoic acid (Pyr-C12) and cis-parinaric acid to nsL-TP, FRET was observed indicating that these fatty acids were accommodated in the lipid binding site closely positioned to the tryptophan residue. Substantial binding was observed only when these fatty acids were presented in the monomeric form complexed to beta-cyclodextrin. As shown by time-resolved fluorescence measurements, translocation of Pyr-C12 from the Pyr-C12-beta-cyclodextrin complex to nsL-TP changed dramatically the direct molecular environment of the pyrene moiety: i.e. the fluorescence lifetime of the directly excited pyrene increased at least by 25% and a distinct rotational correlation time of 7 ns was observed. In order to evaluate the affinity of nsL-TP for intermediates of the beta-oxidation pathway, a binding assay was developed based on the ability of fatty acyl derivatives to displace Pyr-C12 from the lipid binding site as reflected by the reduction of FRET. Hexadecanoyl-CoA and 2-hexadecenoyl-CoA were found to bind readily to nsL-TP, whereas 3-hydroxyhexadecanoyl-CoA and 3-ketohexadecanoyl-CoA bound poorly. The highest affinities were observed for the very-long-chain fatty acyl-CoA esters (24:0-CoA, 26:0-CoA) and their enoyl derivatives (24:1-CoA, 26:1-CoA). Binding of non-esterified hexadecanoic acid and tetracosanoic acid (24:0) was negligible.

Interlayer energy transfer between pyrene-dodecanoic acid and NBD-dodecanoic acid in Langmuir-Blodgett films

The interlayer excitation energy transfer between 12-(1-pyrenyl)dodecanoic acid (PDA), 12-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-y1)-N-methylamino] dodecanoic acid (NBDDA) in LB films has been examined with picosecond time-resolved fluorescence decay measurements. Four fluorescing species are present in PDA LB films: monomer (M), dimer (D) and two types of excimers (E 1 and E 2). The fluorescence of PDA monomers and excimers E 2 is quenched by energy transfer to NBDDA. The critical transfer distances of 40.5 and 40.3 Å for monomers and excimers respectively were calculated.

Membrane Fluidity and Oxygen Diffusion in Cholesterol-Enriched Erythrocyte Membrane

This work studied the effect of cholesteryl hemisuccinate incorporation on membrane fluidity and on the kinetics of oxygen diffusion at different depths in the erythrocyte membrane. Cholesterol concentration in the membrane was expressed as the cholesterol–protein ratio (C/Pt). The membrane fluidity, as assessed by a fluorescence polarization method with diphenylhexatriene and 1-(4-trimethylamino)-6-phenylhexa-1,3,5-triene, decreased as the C/Pt ratio increased. Time-resolved fluorescence spectroscopy of pyrene dodecanoic acid (PDA) under an increasing C/Pt ratio in the erythrocyte membrane revealed enhanced oxygen diffusion in the middle of the membrane bilayer (in which PDA was incorporated), which was not the case with pyrene butyric acid (PBA) incorporated in the internal part of the membrane surface. It has generally been accepted that increased membrane fluidity reduces the physical barrier to oxygen permeation. Such conflicting observations on oxygen permeation in the rigidified erythrocyte membrane could be due to variations in oxygen solubility (preferential partitioning) in different polarity microdomains (cholesterol and phospholipid partitions).

Effect of polyunsaturated fatty acid deficiency on dipole relaxation in the membrane interface of rat liver microsomes

The influence of a fat-free diet on the lipid dynamics of rat liver microsomes and liposomes of microsomal lipids was studied by using different fluorescence methods. Lifetime distribution and rotational diffusion of probes with different localization in the lipid bilayer were measured using multifrequency fluorometry. Lateral mobility was studied by measuring excimer formation of pyrenedodecanoic acid. Dipolar relaxation in the interfacial region was studied using 2-dimethylamino-6-lauroylnaphthalene (Laurdan). In spite of large changes in the fatty acid composition of microsomal lipids, polyunsaturated fatty acid deficiency showed no effect on the lifetime distribution and rotational mobility of 1,6-diphenyl-1,3,5-hexatriene (DPH), 1-(4-(trimethylamino)phenyl)-6-phenyl-1,3,5-hexatriene (TMA-DPH), 2-, 7- and 12-(9-anthroiloxy)stearic acids. The treatment did not change the lateral diffusion of pyrenedodecanoic acid, either. However, generalized polarization of Laurdan fluorescence was higher in polyunsaturated fatty acid deficient microsomes as compared to the polyunsaturated fatty acid sufficient ones. This effect was also observed in liposomes of the total microsomal lipids, indicating that the changes in fatty acid composition resulting from polyunsaturated fatty acid deficiency produced a small but significant decrease in the rate of dipolar relaxation in the region of the lipid polar groups of the bilayer. The absence of lipid gel phase domains in rat liver microsomes was also indicated by Laurdan fluorescence features.

Gramicidin effects on the transverse and lateral distribution of pyrene and pyrene derived probes in lipid bilayers

The excimer to monomer fluorescence intensity ratios obtained by direct excitation and by energy transfer from protein intrinsic tryptophan to pyrene and the enhancement of the 0-0 vibration transition in the monomer fluorescence spectra of pyrene, pyrene methanol (PM) and pyrene dodecanoic acid (PD) have been measured as a function of temperature and gramicidin concentration to investigate the localizations and dynamics of these probes in bilayers of small unilamellar vesicles consisting of egg yolk phosphatidylcholine (EPC) and gramicidin containing EPC liposomes (proteoliposomes). Our measurements reveal that gramicidin does not influence the lateral distribution of PD but reduces the PD excimer formation in the protein environment. On the contrary, PM enriches in the vicinity of gramicidin probably as a result of a fluidity gradient from the phospholipid headgroup region to the protein environment. Pyrene molecules preferentially reside in the neighbourhood of gramicidin for the same reason as given for PM, but are kept away from gramicidin at temperatures below 25°C owing to the rigidity of the outer regions of the membrane.

Effect of a linear (1-octanol) and a branched (2,6-dimethyl-4-heptanol) alkanol upon the properties of dipalmitoylphosphatidylcholine large unilamellar vesicles

We have investigated the effect of the incorporation of a linear (1-octanol) and a branched (2,6-dimethyl-4-heptanol) alkanol into large unilamellar vesicles of dipalmitoylphosphatidylcholine in the gel state upon several properties of the bilayer. The effect was evaluated by measurements of the rate of water outflow following a hypertonic osmotic shock, generalized polarization of 6-dodecanoyl-2-dimethyl)aminonaphthalene (Laurdan), absorption spectra of merocyanine 540 (MC), fluorescence anisotropies of 2-anthroyloxystearic acid (2-AS), 12-anthroyloxystearic acid (12-AS) and diphenylhexatriene (DPH), the lifetimes of pyrene (Py) and pyrenedodecanoic acid (PyD), and the pseudo-first order rate constant of the fluorescence quenching of Py and PyD by oxygen, k ox, as a function of the intravesicular alkanol concentration. The data obtained indicate that the degree of incorporation, and the effect of a given intravesicular concentration of the additive, are extremely dependent on the molecular shape of the alkanol. In particular, the branched alkanol is less soluble and causes greater disorganization of the central parts of the bilayer than the linear one. The incorporation of both additives at low alkanol/lipid ratios produces a notable increase in the rate of water outflow following a hypertonic shock, the effect being more noticeable at low concentrations of the branched alcohol. Both alkanols produce, at least at low concentrations, an increase in the value of 2-AS fluorescence anisotropy, suggesting a more compact organization of the interface. In this region, MC is expelled from the vesicle. At higher 1-octanol concentrations, the fluorescence anisotropy of 2-AS decreases and MC incorporation increases, indicating a biphasic behaviour for the linear alcohol. Significant differences between both alkanols are also observed with respect to their effect upon the values of k ox for PyD, a probe that can be considered to be localized in the inner parts of the bilayer.

Pyrene excitation via resonance energy transfer from protein tryptophan reveals a fluidity gradient in liver microsomes

Membrane fluidity measurements based on excimer formation of pyrene and pyrene derivatives as a measure of lateral diffusion yield a decreased fluidity in the presence of proteins [1,2]. It was the aim of our study to investigate whether the reduced excimer formation is due to a rigidifying effect of proteins on the whole membrane or if the fluorophore mobility is hindered mainly in the immediate protein environment. Resonance energy transfer in microsomal membranes between intrinsic tryptophan residues and pyrene was used to study the excimer formation rate in the vicinity of proteins. The excimer-to-monomer fluorescence ratio after excitation via resonance energy transfer decreased compared to that observed for the direct excitation. The results suggest that, because of the reduced fluidity in the neighborhood of proteins, pyrene and pyrenedodecanoic acid do not diffuse homogeneously in the membrane plane.

Photosensitization of human bladder carcinoma cells by pyrene-dodecanoic acid: quantitative analysis of the cytotoxicity.

The effects of photochemotherapy with the fluorescent fatty acid pyrenedodecanoic acid (P12) and long-wavelength ultraviolet (UVA) light on cells derived from human bladder carcinoma were studied. Exposure of these anchorage-dependent cells to P12 either in monolayers of adherent cells or in suspension resulted in a time-related uptake of P12 and its incorporation into the cells' neutral and phospholipids. The uptake and localization of P12 was visualized with fluorescence microscopy and the distribution of the cell population with respect to P12 uptake was analyzed by flow cytometry. Irradiation of P12-containing monolayers of bladder carcinoma cells with UVA light resulted in cell killing. But, on microscopic examination no apparent cell lysis was detected, and since digestion with trypsin did not result in the dispersion of the monolayers it was impossible to assess toxicity by cell count. Alternative procedures were therefore used, and the following cell parameters were determined: (a) cellular uptake or release of chromate; (b) ability of cells to re-adhere to the substratum; and (c) the long-range proliferation potential. The combined inhibitory effect of photoirradiation on cell adherence and on their proliferative potential was utilized for determining reductions of up to 7 log in cell viability. The results obtained with five independently established in vitro bladder carcinoma cell lines indicated that these cells are susceptible to P12-induced photosensitization, suggesting that bladder malignancies might be potential candidates for pyrene-induced photochemotherapy.

Uptake and degradation of several pyrenesphingomyelins by skin fibroblasts from control subjects and patients with Niemann-Pick disease. Effect of the structure of the fluorescent fatty acyl residue

Three fluorescent analogues of sphingomyelin (SPM), each containing pyrene in the fatty acyl residue, were synthesized and employed for the study of their mode of uptake by, and degradation within, intact cultured human skin fibroblasts. These were prepared by condensing sphingosylphosphocholine and the following fatty acids: pyrenedodecanoic acid (P12), pyrenesulphonylaminoundecanoic acid (PSA11) and pyrenepropenoic acid (P3:1). The cell association and catabolism of these SPM analogues by normal, Niemann-Pick-disease-Type-A and low-density-lipoprotein (LDL)-receptor-negative familial hypercholesterolaemia fibroblasts were investigated and compared with the metabolism of [cholinemethyl-14C]sphingomyelin. The catabolism of the fluorescent derivatives was monitored by measuring the appearance of the corresponding fluorescent ceramides. Two modes of uptake and degradation patterns were observed. Thus P12-SPM and radiolabelled SPM were taken up by LDL-receptor-mediated endocytosis when incubated with serum-containing medium, this conclusion being supported by the very low uptake by familial-hypercholesterolaemia fibroblasts, which lack the apolipoprotein-B/E receptor. After uptake, these compounds were metabolically degraded solely by the lysosomal sphingomyelinase, as evidenced by the fact that more than 98% of the SPM remained undegraded in Niemann-Pick-disease cells. By contrast, PSA11- and P3:1-SPMs were taken up by a receptor-independent endocytic pathway, as indicated by the similar rates of uptake in control and familial-hypercholesterolaemia cells in the absence or presence of fetal-calf serum in the culture medium. The degradation of PSA11-SPM and P3:1-SPM was brought about, in the main, by the lysosomal sphingomyelinase, but also by a yet uncharacterized process. The latter catabolic pathway, active in Niemann-Pick-disease-Type-A fibroblasts, seems to differ from the neutral Mg2(+)-dependent sphingomyelinase whose activity was undetectable in homogenates of skin fibroblasts. The present study emphasizes the influence of the structure of the fatty acyl moiety of SPM on its association with lipoproteins and/or cell membranes and on its intracellular routing and metabolic degradation.

Inactivation of vesicular stomatitis virus by photosensitization following incubation with a pyrene-fatty acid

Vesicular stomatitis virus (VSV) was incubated with pyrene dodecanoic acid (P12), a fluorescent derivative of a medium-chain length fatty acid, and subjected to irradiation with a long wavelength ultra-violet light source at 366 nm (UVA). This inactivated the virus, resulting in a drastic decrease of its infectivity. The virus inactivation was proportional to the concentration of the pyrene-fatty acid, the length of exposure of the virus to P12 and the irradiation dose.

Pyrene-labeled lipids: versatile probes of membrane dynamics in vitro and in living cells

Pyrene-labeled analogs of fatty acids have been studied as probes of lipid metabolism in vitro and in cultured cells. Procedures for the synthesis of complex pyrenyl lipids and the analytical methods for their separation and quantification are described. Pyrenyl-lipids have been used to quantify the relationship between lipid structure and the rates of spontaneous lipid transfer. Modifications of these methods have also been used to monitor protein-mediated lipid transfer, lipolysis and lipid translocation across bilayer membranes. According to several criteria, pyrene dodecanoic acid has been identified as a good analog of some naturally occurring fatty acids. Digital imaging microscopy has been used to monitor the rate of accumulation of pyrenyl lipids in living cells.

Correlation of the dispersion state of pyrene cerebroside sulfate and its uptake and degradation by cultured cells

This study aimed at increasing the efficiency and shortening the time required for administering cerebroside sulfate to cultured cells. For this purpose several modes of dispersion of a fluorescent derivative of cerebroside sulfate (sulfatide), in which the natural fatty acid has been replaced by pyrenedodecanoic acid (P12), were incubated with the cells. This fluorescent derivative of cerebroside sulfate (P12-CS) was introduced into the growth medium of the cells using the three following modes of dispersion: (1) P12-CS was dissolved in dimethylsulfoxide and added to the medium, (2) it was precomplexed with serum albumin or (3) incorporated into small, unilamellar vesicles (SUV) of phosphatidylcholine. With each of these respective modes of dispersion, the P12-CS was incubated for periods up to 48 h with cultured lymphoblasts or fibroblasts. Uptake by the cells could be determined by recording directly the cell-associated fluorescence, using a suspension of washed intact cells. The cell lipids were subsequently extracted with mixtures of chloroform/methanol and their fluorescence recorded. When related to the incubation time, uptake of P12-CS by the cells increased continuously using each of the above dispersions. The appearence of fluorescence at 475 nm (‘excimer’) and the ratio of this to the monomolecular fluorescence at 378 nm (‘ E/ M’) could be used as a measure for the presence of the internalized P12-CS in aggregated or fully dispersed states. These values (i.e., E/ M), recorded on the suspensions of intact cells were rather high using the aqueous dispersions, intermediate values were observed using the SUV and rather low E/ M values (0.5 or less) were observed using the preformed albumin-(P12-CS) complexes. Increasing the mole ratio of albumin to P12-CS (i.e., from 1:2 to 2:1 m/m), decreased the quantity of sulfatide which was taken up by the cells but also further decreased the E/ M ratio, suggesting a fully dispersed state of the pyrene lipid within the cell. This indicated that, using an optimal albumin to P12-CS ratio of 1–2 (or its equivalent values in fetal calf serum) permitted an influx of single molecules of P12-CS into the cells. After 48 h, about 50% of the fluorescence of skin fibroblasts was found in metabolic degradation products of P12-CS. The parallel value for fibroblasts derived from a patient with metachromatic leukodystrophy was only about 5%. Appearance of the excimeric emission of a dispersion of P12-CS in water permitted estimation of its critical micellar concentration as being 7.5 · 10 −7M.

Spectrofluorometric measurements of the dispersion state of pyrenedodecanoic acid and its uptake by cultured cells and liposomes

Pyrene dodecanoic acid (P12), a medium-chain fatty acid to which the fluorescent probe pyrene is covalently linked, showed a considerable increase in fluorescence when the probe was introduced into a hydrophobic environment. Also, when closely packed in an aggregate, an energy transfer between two adjacent molecules of pyrene occurred, resulting in a shift of the peak of the emission spectrum from 378 nm (‘monomeric’) to 475 nm (‘excimeric’). These two respective properties were utilized for the following: (a) A spectrofluorometric measurement of the critical micellar concentration (CMC) of the pyrene fatty acid, defined as the concentration at which the 475 nm emission peak appeared as a consequence of the aggregation of P12 molecules in aqueous solution to form micelles; the CMC of P12 was found to be in the range of 1 to 2 μM. (b) The penetration of P12, from an aqueous solution or dispersion, into unilamellar phospholipid vesicles was determined by monitoring the increase of the fluorescence at 378 nm. The fluorescence increase was time-dependent and proportional to the respective concentrations of P12 or phospholipid vesicles. Substituting the neutral phosphatidylcholine with the negatively-charged phosphatidylserine vesicles resulted in a slower rate as well as lesser total uptake of P12. (c) The uptake of P12 by cells was accompanied by an increase in the monomeric fluorescence emission intensity. Using cells in suspension, this could be followed continuously in a spectrofluorometer equipped with a recorder. The uptake was found to be time-dependent and proportional to P12 concentration.

The lateral fluidity of erythrocyte membranes. Temperature and pressure dependence.

The pressure and temperature dependence of the lateral and rotational fluidity of erythrocyte membranes was investigated by inserting the excimeric membrane probe 1'-pyrenedodecanoic acid (PDA) into the membranes of intact cells and measuring the probe excimer formation rate and the steady-state polarization of the monomer at pressures up to 2000 atm (2 kbar). At that pressure the lateral diffusivity of PDA was found to decrease by a factor of 10 and its emission anisotropy by a factor of 5 at 22 degrees C. At atmospheric pressure, the local lateral diffusion coefficient of PDA at 2 and 33 degrees C is 1.5 and 4.3 x 10(-8) cm2 s-1, respectively. The activation energy for probe translation was found to decrease from 6 to 3 kcal M-1 in going from atmospheric pressure to 2 kbar, while the entropy decreased by approx. 15 cal M-1 K-1, indicating greater lipid order at the high pressure. The experimental data are consistent with a 'free-area' model for the membrane, analogous to the free-volume model for nonassociated liquids. The lateral diffusivity of PDA was found to be proportional to the free membrane area and linear extrapolation to zero diffusivity indicates that at atmospheric pressure, the fractional free area of the erythrocyte membrane is 6%.

Interactions of pyrene derivatives with lipid bilayers and with (Ca2+-Mg2+)-ATPase.

The intensities of fluorescence emission for pyrene and a number of its derivatives increase on binding to lipid bilayers and to the (Ca2+-Mg2+)-ATPase purified from rabbit muscle sarcoplasmic reticulum. The effect is particularly marked for the less water-soluble derivatives. Changes in intensity for monomer and excimer emission as a function of lipid concentration can be fitted to a simple model to obtain binding parameters. The number of binding sites per lipid is 0.2-0.4. For the ATPase system, at least two classes of sites are necessary to fit the data, one corresponding to the lipid component and one to sites on the ATPase. Excimer emission from the postulated sites on the ATPase is less marked than that from lipid. Pyrene-dodecanoic acid and pyreneundecyltrimethylammonium bromide, which bind to a large number of sites on the ATPase, cause marked inhibition of ATPase activity at high concentration. Pyrene and a number of water-soluble derivatives cause stimulation of the ATPase reconstituted with dimyristoleoylphosphatidylcholine and little inhibition and bind to a small number of sites on the ATPase. It is concluded that excimer emission from pyrene derivatives in systems containing proteins cannot be used to obtain reliable information about rates of diffusion in the lipid component of the membrane.