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  • 1
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 4 (1976), S. 449-465 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The use of conjugated polyene fatty acids as probes of membrane structure is examined. α- and β-parinaric acid (cis, trans, trans, cis- and all trans-9,11,13,15-octadecatetraenoic acid) and synthetic lecithins containing an α-parinaric acid chai in position 2 have been prepared, and their absorption and fluorescence properties have been determined. Their absorption spectra are at sufficiently long wavelength to be unobscured by cellular chromophores such as nucleotides and aromatic amin acids. Parinaric acid absorption does, however, overlap tryptophan emission which allows fluorescence energy transfer.Potential uses of these fluorescent probes are presented with studies on mode systems with known physical properties. Dipalmitoyl phosphatidylcholine exhibits a sharp phase transition 1° wide at 42° C, as monitored by the fluorescence intensit, of parinaric acid. The magnitude of the transition is independent of probe concentration, but the width of the transition and hysteresis are dependent upon such factors as the probe concentration and whether or not sonication is used in sample preparation. Using both fluorescence and absorption properties of the probe, we show that the addition of cholesterol to the dispersion broadens and decreases the magnitude of the transition. These results are interpreted in terms of a change in the polarizability of the acyl chains of a lipid bilayer as the bilayer undergoes a thermal transition.Lipid-protein interactions are studied by the binding of α-parinaric acid to bovine serum albumin. Fluorescence enhancement, absorption spectral shifts, and quenching of tryptophan fluorescence are observed when α-parinaric acid binds to bovine serum albumin. Calculations based on these measurements are consistent with two binding sites of KB ∼ 108 (M-1) and three to four binding sites of KB ∼ 106 - 107 (M-1), similar to known values for the binding of other long-chain fatty acids.Biosynthetic incorporation of β-parinaric acid into the E. coli fatty acid auxotroph 30E βox- has been accomplished and phase transitions in cells and isolated phospholipids are shown.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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