Adhesion ability of angiotensin II with model membranes.

The octa-peptide angiotensin II (Ang II, (HNAspArgValTyrIleHisProPheCOOH)) is one of the key player on blood pressure regulation in mammals. Predominantly binding to the Angiotensin type 1 and 2 receptors, the hormone is one of several peptide ligands binding to G protein coupled receptors (GPCR). The active hormone derives from a high molecular weight precursor sequentially cleaved by the proteases renin and the angiotensin converting enzyme (ACE).

On the Interaction between Digitonin and Cholesterol in Langmuir Monolayers.

In this article, we describe the effect of a highly hemolytic saponin, digitonin, on model lipids cholesterol and dipalmitoylphosphatidylcholine (DPPC) using a combination of tensiometric (surface pressure and dilatational surface elasticity), spectroscopic (infrared reflection absorption spectroscopy, IRRAS), microscopic (fluorescence microscopy), and scattering techniques (neutron reflectivity, NR, and grazing incidence X-ray diffraction, GIXD). The monolayers of individual lipids and their 10:9 (mol/mol) mixture were exposed to an aqueous solution of digitonin (10(-4) M) by subphase exchange using a setup developed recently in our laboratory. The results confirm that digitonin can adsorb onto both bare and lipid-covered water-air interfaces.

Complexation of phospholipids and cholesterol by triterpenic saponins in bulk and in monolayers.

The interactions between three triterpene saponins: α-hederin, hederacoside C and ammonium glycyrrhizate with model lipids: cholesterol and dipalmitoylphosphatidylcholine (DPPC) are described. The oleanolic acid-type saponins (α-hederin and hederacoside C) were shown to form 1:1 complexes with lipids in bulk, characterized by stability constants in the range (4.0±0.

Reverse hydrotropy by complex formation.

Self-aggregation of three di-N-alkylated diaza-18-crown-6 ethers (ACEs) was studied in non-polar solvents. The three ACEs differed by the length of the alkyl chain: n-decyl (ACE-10), n-hexadecyl (ACE-16) and n-tetracosane (ACE-24). From the previously reported interfacial tension isotherms, the formation of reverse micelles was expected above ACE concentrations of ∼10(-3) M.

Unusual penetration of phospholipid mono- and bilayers by Quillaja bark saponin biosurfactant.

The interactions between a model phospholipid 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and a biosurfactant Quillaja Bark Saponin (QBS) obtained from the bark of Quillaja saponaria Molina were studied using simple models of biological membranes. QBS is known to interact strongly with the latter, exerting a number of haemolytic, cytotoxic and anti-microbial actions. The interaction of QBS dissolved in the subphase with DPPC monolayers and silicon-supported bilayers was studied above the cmc (10(-3)M).

Effect of hydration of sugar groups on adsorption of Quillaja bark saponin at air/water and Si/water interfaces.

Adsorption of a natural glycoside surfactant Quillaja bark saponin ("QBS", Sigma Aldrich 84510) was studied at the air/water and Si/water interfaces using a combination of surface pressure (SP), surface dilatational rheology, neutron reflectivity (NR), Infra-Red Attenuated Total Reflection Spectroscopy (IR ATR) and Quartz Crystal Microbalance (QCM). The adsorbed layers formed at the air/water interface are predominantly elastic, with the dilatational surface storage modulus reaching the maximum value of E'=184 mN/m. The NR results point to a strong hydration of the adsorbed layers (about 65% hydration, corresponding to about 60 molecules of water per one QBS molecule), most likely related to the presence of multiple sugar groups constituting the glycone part of the QBS molecules.

High hydrostatic pressure effects investigated by neutron scattering on lipid multilamellar vesicles.

The effects of high hydrostatic pressure on the structure and dynamics of model membrane systems were investigated using neutron scattering. Diffraction experiments show shifts of the pre- and main-phase transitions of multilamellar vesicles of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) to higher temperatures with increased pressure which are close to results observed previously by other techniques, namely (10.4 ± 1.

Surfactant mixtures at the oil-water interface.

We report the structural study of mixed monolayers of partially deuterated N,N'-di-hexadecyl-(d33)-4,13-diaza-18-crown-6 ether (d-ACE16) and palmitic acid (PA) at the oil-water interface, in order to understand the mechanism of metal ion transport through Permeation Liquid Membrane (PLM) devices. The composition of the mixed monolayers remains constant with increasing spread amount and the saturation of the interface is achieved at a relatively low spread amount. The excess PA material is accommodated in the oil phase, playing an important role in equilibrating the interfacial concentration of ACE-16.

Use of small angle neutron scattering to study the interaction of angiotensin II with model membranes.

Understanding biological processes assumes a detailed understanding of the interaction of all involved molecules. Here the effect of the peptide hormone angiotensin II (Ang II), an agonist of the angiotensin receptors, on the structure of unilamellar and multilamellar dimyristoyl phosphatidylcholine vesicles was studied by small angle neutron scattering, dynamic light scattering and differential scanning calorimetry. The calorimetry data indicate a weak interaction of Ang II with the surface of the membrane bilayer, as the pretransition persists during all experiments, and the main transition is only slightly shifted towards higher temperatures.

Hydration dependent studies of highly aligned multilayer lipid membranes by neutron scattering.

We investigated molecular motions on a picosecond timescale of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) model membranes as a function of hydration by using elastic and quasielastic neutron scattering. Two different hydrations corresponding to approximately nine and twelve water molecules per lipid were studied, the latter being the fully hydrated state. In our study, we focused on head group motions by using chain deuterated lipids.

Absorption of light and heavy water vapours in polyelectrolyte multilayer films.

We studied the swelling and the uptake of water (H(2)O or D(2)O) vapours in polyelectrolyte (PE) multilayer (PEM) samples deposited on solid support (Si wafers) as a function of the isotope nature of the vapour and the charge of the last polymer layer. The samples were prepared with deuterated poly(sodium 4-styrenesulfonate) (dPSS) and poly(allylamine hydrochloride) (PAH). Two types of samples were studied.

Ordering of Fe(3)O(4) nanoparticles in polyelectrolyte multilayer films.

In our work we have focused on the incorporation of magnetite nanoparticles (NPs) into poly(allylamine hydrochloride)/poly(sodium 4-styrenesulfonate) polyelectrolyte multilayers (PEMs). The main goal of presented studies was to control the two-dimentional ordering of NPs within polyelectrolyte films. The ordering of NPs depended on the treatment of the underlying polyelectrolyte films.

Interaction of the MARCKS peptide with PIP2 in phospholipid monolayers.

In this present work we have studied the effect of MARCKS (151-175) peptide on a mixed DPPC/PIP2 monolayer. By means of film balance, fluorescence microscopy, x-ray reflection/diffraction and neutron reflection measurements we detected changes in the lateral organization of the monolayer and changes in the perpendicular orientation of the PIP2 molecules depending on the presence of MARCKS (151-175) peptide in the subphase. In the mixed monolayer, the PIP2 molecules are distributed uniformly in the disordered phase of the monolayer, whereas the PI(4,5) groups elongate up to 10 A below the phosphodiester groups.

Layer-by-layer deposition of polyelectrolytes. Dipping versus spraying.

We studied the properties of polyelectrolyte multilayer films prepared using the technique of polyelectrolyte deposition from solution (dipping) or supplying the solutions to the surface by spraying. The quality of films obtained by those two techniques was compared to find out whether the well-established dipping procedure can be replaced with the spraying technique. Neutron and X-ray reflectometric studies were performed on the samples of interest.

Thermal stability, mechanical properties and content of bacterial protein layers recrystallized on polyelectrolyte multilayers.

The influence of the temperature on the surface topology, layer thickness and density of recrystallized bacterial S-layers from Bacillus sphaericus CCM2177 on polyelectrolyte multilayers in contact with liquid water was investigated. A quartz crystal microbalance with dissipation (QCM-D) was used to monitor the build-up of the polyelectrolyte multilayer and the adsorption of S-layer protein (1600 ng cm-2). The critical temperature (55 °C) at which the S-layer loses its 2-D structure was obtained from atomic force microscopy (AFM) and confirmed by neutron reflectometry (NR) experiments.

Control of protein interfacial affinity by nonionic cosolvents.

In a biological cell, proteins perform their functions in a highly complex environment comprising crowding and confinement effects as well as interactions with interfaces, cosolvents, and other biomolecules. Cosolvents can stabilize or destabilize the native folded structure of proteins in solution. In this study, we show that nonionic cosolvents also affect the interfacial affinity of proteins.

Structure and protein binding capacity of a planar PAA brush.

We performed neutron reflectometry (NR) and total internal reflection fluorescence (TIRF) spectroscopy to characterize the structure and the protein binding capacity of a planar poly(acrylic acid) (PAA) brush at different temperatures. A PAA brush was prepared by spin-coating planar quartz or silicon wafers with a thin film of poly(styrene). Then, the diblock copolymer poly(styrene)-poly(acrylic acid) was deposited on these modified wafers using the Langmuir-Schäfer or Langmuir-Blodgett technique.

Neutron reflectometry and spectroscopic ellipsometry studies of cross-linked poly(dimethylsiloxane) after irradiation at 172 nm.

Poly(dimethylsiloxane) (PDMS) was irradiated under ambient conditions in air with a Xe2-excimer lamp. The formation of atomic oxygen and ozone during irradiation in air by V-UV photons results in the transformation of PDMS to silicon oxide. The irradiated surfaces were studied by spectroscopic ellipsometry and neutron reflectometry.

Formation of polyelectrolyte multilayer architectures with embedded DMPC studied in situ by neutron reflectometry.

The coupling of lipid molecules to polymer components in a planar biomimetic model membrane made of a lipid bilayer (dimyristoylphosphatidylcholine) supported by polyelectrolyte multilayers is studied. The polyelectrolyte support was prepared by layer-by-layer deposition of positively charged poly(allylamine hydrochloride) (PAH) and negatively charged poly(sodium 4-styrenesulfonate) (PSS). Two polymer sample terminations were considered: positively charged (PAH-terminated) and negatively charged (PSS-terminated).

Structural, volumetric, and thermodynamic characterization of a micellar sphere-to-rod transition.

The thermotropic sphere-to-rod transition of nonionic surfactants was characterized in terms of a large set of parameters: the transition temperature and width, the partial volume, coefficient of thermal volume expansion, enthalpy, isobaric heat capacity, and structural parameters, such as radius of gyration and hydrodynamic radius. Data were recorded as a function of concentration of surfactants in H2O and in D2O. To this end, pressure perturbation calorimetry (PPC), small angle neutron scattering (SANS), dynamic light scattering (DLS), differential scanning calorimetry (DSC), and isothermal titration calorimetry (ITC) were applied in a study of aqueous solutions containing myristyl, tridecyl, and lauryl maltoside and heptaethyleneglycoltetradecyl ether (C14EO7).

Membrane insertion of a lipidated ras peptide studied by FTIR, solid-state NMR, and neutron diffraction spectroscopy.

Membrane binding of a doubly lipid modified heptapeptide from the C-terminus of the human N-ras protein was studied by Fourier transform infrared, solid-state NMR, and neutron diffraction spectroscopy. The 16:0 peptide chains insert well into the 1,2-dimyristoyl-sn-glycero-3-phosphocholine phospholipid matrix. This is indicated by a common main phase transition temperature of 21.