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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 34 (1995), S. 4684-4688 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 25 (1996), S. 55-59 
    ISSN: 1432-1017
    Keywords: Key words Melittin ; Phosphatidylcholine ; Phosphatidic acid ; Cholesterol ; Membrane defects ; 31P-NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Since many studies on peptide-membrane interactions are carried out only with fluid phase lipid bilayers (L α -phase, absence of cholesterol) we have investigated whether this phase is really a suitable model for biological membranes. For this purpose the action of melittin on zwitterionic and negatively charged phospholipid bilayers, in the absence and presence of 30 mol% cholesterol, was investigated by solid state 31P-NMR. From the NMR point of view, it appears that systems composed of a single phospholipid best mimic the sterol-containing system a few degrees below the gel-to-fluid phase transition, i. e., in the rippled phase (P β' ). It is then proposed that a relatively rigid membrane containing local defects, rather than a L α -bilayer, is required as an appropriate model for natural membranes when probing the action of melittin. Such requirements might be crucial when studying peptide-lipid interactions.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1017
    Keywords: 2H-NMR ; filipin ; DMPC ; circular dichroism ; model membranes ; carboxyfluorescein release
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Interaction of the pentene antibiotic filipin with dimyristoylphosphatidylcholine (DMPC) membranes has been monitored by 2H-NMR, circular dichroism (CD), electronic absorption and fluorescence in the temperature range 10° to 60°C. Interaction appears to depend on whether filipin is added before or after membrane formation and also upon the temperature of the system. When filipin is added to preformed DMPC large unilamellar vesicles (LUV), the association constants, as determined by electronic absorption are 39×103 M -1, 15×103 M -1 and 0.6×103 M -1 at 15°, 30° and 50°C, respectively. Under identical conditions, CD spectra of bound filipin exhibit features characteristic of an aggregation over the whole temperature range. When filipin is incorporated in membranes during their preparation, the 2H-NMR spectra of deuterated DMPC indicate that the drug has a slight disordering effect on the lipid matrix below the temperature, T c ,of the gel-to-fluid phase transition and above T c +11°C. Between these two temperature boundaries the system consists of two lipid regions of very different dynamic properties. One of the regions, which is attributed to a filipin-lipid complex, has the properties of gel-like lipids whereas the other has those of fluid-like lipids. The latter domain is however more ordered than the pure lipid at corresponding temperatures. CD spectra under the same conditions are found to be identical to spectra when the drug is added to preformed membranes, only in the region T c to T c +11°C. Filipin induced carboxyfluorescein release from DMPC-LUV is found to be complete when the filipin-to-lipid ratio is near 1, for temperatures below T c +11°C. Results are compared to previous data on amphotericin B and provide evidence that the gel-like structure of phospholipid and membrane permeation may be induced by filipin even in the absence of cholesterol.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-2932
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Phosphatidylethanolamine (PE), phosphatidylserine (PS) and phosphatidylcholine (PC) in micellar phase in water have been studied by high resolution phosphorus-31 nuclear magnetic resonance (31P-NMR), in order to follow inorganic mercury Hg(II) binding to the lipid headgroups. Decrease of the NMR peak area is observed upon HgCl2 addition, with greater effect on PE and PS compared to PC. This is interpreted by Hg(II) binding to several phospholipid headgroups, linking different micelles together and forming by extension a large “insoluble” phospholipid-mercury network that is undetectable by high-resolution31P-NMR. The extent of phospholipid aggregation depends on the mercury-to-lipid molar ratio, and apparent Hg(II) affinities to phospholipid headgroups are in the order PE〉PS〉〉PC. When HgCl2 is added to mixed micelles prepared with two lipids (PE/PC or PS/PC), co-precipitation is observed for both components in similar proportions.
    Type of Medium: Electronic Resource
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