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Perturbation of phospholipid bilayers by DDT
Biochimica Et Biophysica Acta
|January 26, 1987
Summary
The addition of DDT to lipid bilayers fluidizes membranes, with increased microviscosity starting from the center and moving outward in DPPC bilayers. DDT also slightly lowers the phase transition temperature of DPPC bilayers.
Area of Science:
- Biochemistry
- Membrane Biophysics
- Lipid Bilayer Dynamics
Background:
- Understanding how environmental factors affect cell membrane properties is crucial.
- Phosphatidylcholines like DPPC and egg PC are key components of biological membranes.
- DDT (dichlorodiphenyltrichloroethane) is a known environmental contaminant with potential membrane interactions.
Purpose of the Study:
- To investigate the localization of DDT's effects on acyl chain dynamics in phosphatidylcholine bilayers.
- To determine how DDT concentration influences membrane fluidity and structure.
- To examine DDT's impact on the phase transition temperature of lipid bilayers.
Main Methods:
- Steady-state fluorescence polarization using n-(9-anthroyloxy) fatty acid probes at various depths.
- Investigated unilamellar vesicles of DPPC and egg PC with varying DDT concentrations (5-50 mol%).
- Measured changes in microviscosity and fluorescence lifetime.
Main Results:
- DDT acts as a fluidizer for both DPPC and egg PC bilayers.
- Increased microviscosity in DPPC bilayers at 23°C initiated at the bilayer center and progressed outward with increasing DDT.
- DDT (33 mol%) reduced the phase transition temperature of DPPC bilayers by ~2°C; no significant effect on fluorescence lifetime observed.
Conclusions:
- DDT's fluidizing effect is localized and concentration-dependent within lipid bilayers.
- The impact of DDT on membrane microviscosity differs between gel and fluid phases.
- DDT does not significantly alter the excited-state fluorescence lifetime of probe molecules in these lipid systems.

