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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 1070 (1991), S. 259-264 
    ISSN: 0005-2736
    Keywords: (E, coli) ; Fluorescence ; Lipid membrane ; Permeability ; Tachyplesin I
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 267 (1989), S. 520-524 
    ISSN: 1435-1536
    Keywords: Mixedsurfactant ; liposome ; lysis ; solubilization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Interactions of the mixed surfactant solution of dodecylamido propyl dimethyl aminoacetate and sodium dodecyl sulfate with the liposomal membrane were studied. Lytic activities of the surfactants were measured as a function of the concentrations of surfactant and phospholipid and the composition of mixed surfactants. The solubilization limits of phospholipid by surfactants were determined from the change of their aggregation behavior in suspensions at equilibrium by means of quasi-elastic light scattering. The mixed surfactant solutions showed lower lytic activity than single component surfactant solution in spite of the strong adsorption onto the liposome surface. This was attributed to low solubilization power of binary mixture for phospholipid.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 267 (1989), S. 201-208 
    ISSN: 1435-1536
    Keywords: Polyoxyethylene cholesteryl ethers ; liposome ; membrane-lysis ; membrane fluidity ; activation energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In order to deduce the mechanisms of hemolysis induced with the nonionic surfactants, polyoxyethylene cholesteryl ethers, C27H45(OCH2CH2) n OH (n=8, 25, 30, 50) and polyoxyethylene dihydrocholesteryl ethers, C27H47(OCH2CH2) n OH (n=15, 30, 50), the interaction of these surfactants with the liposomal membrane as a simple model membrane was investigated in terms of a leakage of the entrapped marker, and a change of the membrane fluidity. The time-courses of the marker leakage were characterized with two kinetic parameters, the initial induction period and the apparent first-order rate constant. The polyoxyethylene chain length was an important factor in the membrane-lytic activities, and the maximal rate as well as the maximal amount of the marker leakage was observed with n=25–30 in these surfactants series. However, the apparent activation energies derived from the two kinetic parameters increased almost linearly with the hydrophilic chain length. The used surfactants tended to fluidize the liposomal membrane in the concentration ranges of surfactants where the marker leakage is not at all or only slightly induced — but with the higher concentration of the cholesteryl derivatives, the apparent fluidity was significantly reduced. From these observations, the mechanisms of the membrane-lysis are discussed.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1435-1536
    Keywords: Tachyplesin I ; lipid membrane ; permeability ; aggregation ; fusion ; micellization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Tachyplesin I, a broad-spectrum antimicrobial peptide fromTachypleus tridentatus has a basic (+7), amphiphilic, and cyclic β-sheet structure. We reported (Matsuzaki K. et al. (1991) Biochim. Biophys. Acta 1070:259–264) that 1) the action mechanism of tachyplesin I may be the permeabilization of bacterial membranes, 2) the peptide specifically permeabilizes acidic phospholipid bilayers, and 3) its Trp2 residue is located in the hydrophobic region near the surface of the bilayers. In this paper, we found that tachyplesin I dose-dependently induces not only the permeabilization but also aggregation/fusion and micellization of the phosphatidylglycerol large unilamellar vesicles (100 nm in diameter) either in the gel (L-α-dipalmitoylphosphatidyl-DL-glycerol (DPPG)) or liquid-crystalline (egg yolk L-α-phosphatidyl-DL-glycerol (egg PG)) phase, as revealed by light scattering and electron micrograph techniques. The solid DPPG vesicles were more susceptible to the peptide. At peptide to lipid molar ratios (P/L) of 1/500 to 1/200, interpeptide interactions formed a pore through which calcein, a fluorescent dye, can leak out of the vesicles. The pore lifetime was longer in the DPPG vesicles. Further addition of the peptide caused aggregation and/or fusion of the vesicles. At a charge-neutralizingP/L ratio of 1/7, the enlarged vesicles disintegrated into small spherical particles (10–20 nm in diameter). The mechanism for these morphological changes will be discussed.
    Type of Medium: Electronic Resource
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