Gossypol (1,1 ',6,6 ',7,7'-hexahydroxy-5,5 ' -diisopropyl-3,3 '-dimethyl[2,2'-binaphthalene]-8,8' dicarboxaldehyde) previously used as a male oral contraceptive is an amphiphilic compound. At low concentrations, it is expected that gossypol would intercalate into the phospholipid bilayers. To demons
The effects of phosphatidylethanolamine and phosphatidylglycerol headgroups on bilayer dynamics: a slow-motion ESR study
โ Scribed by Leo J. Korstanje; Klass A. Eikelenboom; Christoph S. van der Reijden; G. van Ginkel; Yehudi K. Levine
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 671 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0009-3084
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โฆ Synopsis
A study of the effect of phosphatidylethanolamine and phosphatidylglycerol headgroups on the behaviour of cholestane spinlabel (CSL) molecules in three fipid bilayer configurations: planar muitibilayers, multilamellar liposomes and small unilamellar vesicles (SUV) is presented. The results are compared with those obtained from the corresponding configurations of phosphatidylcholines with identical acyl chain composition.
A comparison of the parameters describing the orientationai order and dynamics of CSL in palmitoyloleoylphosphatidylethanolamine (POPE) and paimitoyloleoylphosphatidylcholine (POPC) bilayer configurations indicates that the hydration of the lipid headgroups is the most important factor determining the rates of rotational motion.
The orientational order of CSL is found to be lower in fully hydrated muitilamellar liposomes and SUVs of negatively charged dioleoylphosphatidylglycerol (DOPG), than in the same configurations of the zwitterionic dioleoylphosphatidylcholine (DOPC). However, the rotational diffusion is not affected by the difference in the lipid headgroup. Apparently, the electrostatic repulsion in DOPG multilamellar liposomes and SUVs causes the orientational order to decrease, but without affecting the rates of rotational diffusion.
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