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An ordered metastable phase in hydrated phosphatidylethanolamine: the Y-transition
B Tenchov1, R Koynova, M Rappolt
1Institute of Biophysics, Bulgarian Academy of Sciences, Acad. G. Bonchev str. 21, 1113, Sofia, Bulgaria. tenchov@obzor.bio21.bas.bg
Biochimica Et Biophysica Acta
|March 17, 1999
Summary
Researchers discovered a new metastable ordered phase, the LR1 phase, in dihexadecylphosphatidylethanolamine (DHPE) lipids. This phase forms rapidly at low temperatures and exhibits unique hydrocarbon chain arrangements, offering insights into lipid polymorphism.
Area of Science:
- Lipid polymorphism and phase behavior
- Materials science of phospholipids
- Supramolecular chemistry
Background:
- Dihexadecylphosphatidylethanolamine (DHPE) is a phospholipid with complex phase behavior.
- Understanding lipid phase transitions is crucial for biological membranes and material applications.
- Low-temperature phases in lipids can exhibit unique structural arrangements.
Purpose of the Study:
- To investigate the low-temperature phase behavior of fully hydrated dihexadecylphosphatidylethanolamine (DHPE).
- To characterize a newly observed metastable ordered phase in DHPE.
- To elucidate the formation pathway and properties of this novel lipid phase.
Main Methods:
- Time-resolved X-ray diffraction to analyze structural changes.
- Differential scanning calorimetry to detect thermal transitions.
- Scanning densitometry to measure volume changes during phase transitions.
Main Results:
- Rapid formation of a metastable LR1 phase in DHPE at approximately 12°C upon cooling.
- The LR1 phase exhibits an orthorhombic hydrocarbon chain arrangement, distinct from the Lβ phase.
- The LR1 phase is readily reversible with minimal hysteresis and is a precursor to the Lc phase.
Conclusions:
- The LR1 phase represents a novel low-temperature ordered state in DHPE lipids.
- The formation of the equilibrium Lc phase primarily occurs from the LR1 phase.
- DHPE's low-temperature polymorphism shares similarities with long-chain normal alkanes.