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Journal of Lipid Research, Vol 36, 1936-1944, Copyright © 1995 by Lipid Research, Inc.
J Shah, JM Atienza, RI Duclos Jr, AV Rawlings, Z Dong and GG Shipley
Differential scanning calorimetry (DSC) and X-ray diffraction techniques
have been used to investigate the structure and thermotropic properties of
synthetic, non-hydroxy fatty acid (16:0) ceramide (NFA(C16)CER) as a
function of hydration. Anhydrous NFA(C16)CER shows a single, broad
endothermic transition at 95.4 degrees C (delta H = 10.4 kcal/mol). On
hydration, a broad exothermic transition appears at approximately 50-70
degrees C while the main endothermic transition decreases to 90.0 degrees C
(delta H = 13.8 kcal/mol). The enthalpy of the exothermic transition
increases with hydration to a maximum value, delta H = 4.8 kcal/mol. This
polymorphic phase behavior depends on the low temperature incubation time
and prior cooling rate. X-ray diffraction of fully hydrated NFA(C16)CER at
26 degrees C, shows a well- ordered lamellar phase with a bilayer
periodicity d = 46.9 A. At 68 degrees C, above the first exothermic
transition, X-ray diffraction shows again a lamellar phase with reduced
bilayer periodicity d = 41.8 A and an increased number of both lamellar and
wide-angle reflections indicative of enhanced layer and chain packing
order, respectively. At 90.0 degrees C, above the main transition, the
diffraction pattern shows a broad, intense reflection at 29.9 A and a
diffuse reflection at 4.6 A, indicative of a melted chain phase. On
cooling, NFA(C16)CER exhibits polymorphic phase behavior involving the
conversion of the melted chain phase to a metastable bilayer phase. On
heating, this metastable phase undergoes an exothermic transition to a
stable bilayer phase; on further heating, NFA(C16)CER converts
endothermically to the melted-chain phase.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Structural and thermotropic properties of synthetic C16:0 (palmitoyl) ceramide: effect of hydration
Department of Biophysics, Boston University School of Medicine, MA 02118, USA.
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