Lipid Bilayer Surface Interaction
Mostrando 1-12 de 31 artigos, teses e dissertações.
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1. Development of membrane biosensors and characterization of the interactions between cytochrome c and hybrid bilayer membranes by Surface Plasmon Resonance / Desenvolvimento de biosensores de membranas e caracterização da interação entre citocromo c e bicamadas híbridas por ressonância plasmônica de superfície
The aim of this work was to develop membrane biosensors based on Surface Plasmon Resonance (SPR) and to apply them to study the interactions between cytochrome c (cyt c) and model membranes. SPR is an optical technique that provides high-sensitivity measurements of refractive index (n), allowing the characterization of the adsorption and desorption of molecu
Publicado em: 2008
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2. Estudos estruturais de histatina-5 e seu análogo, TOAC0-histatina-5: interação com metais e sistemas biomiméticos / Structural studies of Histatin-5 and its analogue, TOAC0-Histatin-5: interaction with metals and biomimetic systems
The mechanism of action of histatin-5 (Hst-5), an antifungal antimicrobial peptide from human saliva is not completely clarified. Circular dichroism (CD), fluorescence, and electron paramagnetic resonance (EPR) were used to examine the conformational behavior of Hst-5 and its analogue containing the paramagnetic amino acid TOAC at the N-terminus (TOAC0-Hst-5
Publicado em: 2008
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3. Propriedades de vesículas unilamelares gigantes / Properties of Giant Unillamelar Vesicles
The stability of giant unilamellar vesicles (GUVs) has been monitored by phase contrast and fluorescence microscopy, using sugar gradients, sodium 1,3,6,8 pirene tetrasulfonate (PTS) as fluorescent probe, 1,1-dimethyl-4,4-bipiridinium chloride (MV) as fluorescence quencher and 2-(12-(7-nitrobenz-2-oxa-1,3-diazol-4-il) amino) dodecanoyl-1-hexadecanoyl-sn-glic
Publicado em: 2006
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4. Interações entre bicamadas lipídicas e interfaces hidrofóbicas / Interactions between lipid bilayers and hydrophobic interfaces
Determinations of surface tension (γ) at the air--water interface, contact angles (Θ), and in and ex-situ ellipsometric mean thickness (d) were used to study the interaction between dioctadecyldimethylammonium bromide (DODAB) small vesicles and spin-coated polystyrene sulfate (PSS) films on silicon wafers. Upon the adition of NaCl (50 mM final conc
Publicado em: 2003
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5. Octyl-beta-D-glucopyranoside partitioning into lipid bilayers: thermodynamics of binding and structural changes of the bilayer.
The interaction of the nonionic detergent octyl-beta-D-glucopyranoside (OG) with lipid bilayers was studied with high-sensitivity isothermal titration calorimetry (ITC) and solid-state 2H-NMR spectroscopy. The transfer of OG from the aqueous phase to lipid bilayers composed of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) can be investigated by emp
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6. Molecular reorganization of lipid bilayers by complement: a possible mechanism for membranolysis.
The interaction between the membrane attack complex (MAC) of complement and flat lipid bilayers was investigated. Using spin-labeled derivatives of phospholipids and cholesterol and electron paramagnetic resonance spectroscopy, we measured the penetration of the MAC into bilayers and its influence on the order of bilayers. The MAC precursor components C5b--6
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7. Interaction of dystrophin fragments with model membranes.
The interaction with membrane lipids of recombinant fragments of human dystrophin, corresponding to a single structural repeating unit of the rod domain, was examined. Surface plasmon resonance, constant-pressure isotherms in a Langmuir surface film balance, and interfacial rheology were used to observe binding of the polypeptides and its effects on the prop
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8. Surface plasmon resonance studies of complex formation between cytochrome c and bovine cytochrome c oxidase incorporated into a supported planar lipid bilayer. I. Binding of cytochrome c to cardiolipin/phosphatidylcholine membranes in the absence of oxidase.
The mechanism of interaction between cytochrome c and a solid-supported planar phosphatidylcholine membrane containing varying amounts of cardiolipin (0-20 mol%) has been studied over a wide range of protein concentrations (0-450 microM) and ionic strength conditions (10-150 mM), by direct measurement of protein binding using surface plasmon resonance (SPR)
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9. Phospholipid bilayer surface configuration probed quantitatively by 31P field-cycling NMR
31P relaxation of the diester phosphate of phospholipids in unilamellar vesicles has been studied from 0.004 to 11.7 T. Relaxation at very low fields, below 0.1 T, shows a rate increase that reflects a residual dipolar interaction with neighboring protons, probably dominated by the glycerol C3 protons. This interaction is not fully averaged by faster motion
National Academy of Sciences.
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10. Membrane binding of β2-glycoprotein I can be described by a two-state reaction model: an atomic force microscopy and surface plasmon resonance study
Complexes formed between β2GPI (β2-glycoprotein I), a human plasma protein, and biological membranes are considered to be targets of macrophages and antiphospholipid autoantibodies involved in autoimmune diseases, such as antiphospholipid syndrome or systemic lupus erythematosus. The positively charged lysine-rich fifth domain of β2GPI facilitates its int
Portland Press Ltd..
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11. Membrane binding of the colicin E1 channel: activity requires an electrostatic interaction of intermediate magnitude.
In vitro channel activity of the C-terminal colicin E1 channel polypeptide under conditions of variable electrostatic interaction with synthetic lipid membranes showed distinct maxima with respect to pH and membrane surface potential. The membrane binding energy was determined from fluorescence quenching of the intrinsic tryptophans of the channel polypeptid
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12. A molecular model for lipid-protein interaction in membranes: the role of hydrophobic mismatch.
The interaction free energy between a hydrophobic, transmembrane, protein and the surrounding lipid environment is calculated based on a microscopic model for lipid organization. The protein is treated as a rigid hydrophobic solute of thickness dP, embedded in a lipid bilayer of unperturbed thickness doL. The lipid chains in the immediate vicinity of the pro