Deuterated methylene groups have been introduced synthetically in selected positions of the sn-2 palmitoyl chain of 1,2-dipalmitoylom-glycero-3-phosphocholine (DPPC) and deuterated methyl groups in the sn-1 and sn-2 palmitoyl chains as well as in the m-3 phosphocholine group. The vibrational spectr
Structural properties of a monobrominated analog of 1,2-dipalmitoyl-sn-glycero-3-phosphorylcholine
✍ Scribed by R.K. Lytz; J.C. Reinert; S.E. Church; H.H. Wickman
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 697 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0009-3084
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✦ Synopsis
Hydrated multibilayers of 1-palmitoyl-2-monobromopalmitoyl-sn-glyeero-3-phosphorylcholine (BrDPPC), where the 2-chain is brominated at either the C-9 or C-10 position, have been studied by low and wide angle X-ray diffraction methods. Oriented and unoriented samples were investigated. The long spacing was observed over the temperature interval -15°C to 80°C. A monotonic increase from approx. 50 A to approx. 62 A (28 wt. % H20) occurred with decreasing temperature. The BrDPPC showed no evidence of a sharp gel-toqiquid crystal phase transition. Wide angle scattering showed a diffuse peak corresponding to (4.5 A) -t. Differential scanning calorimetry measurements for hydrated liposomes (50 wt. % H~O) also showed no evidence for a phase transition (-40 < T < 60°C). These results suggest a low temperature amorphous (glass) state for the acyl side chains of BrDPPC. Monolayer film properties of monobrominated stearic acid also reflect a chain disordering effect occurring upon midchain substitution.
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