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Biophys J, April 2000, p. 1921-1931, Vol. 78, No. 4
The Hormel Institute, University of Minnesota, Austin, Minnesota 55912 USA
Sphingomyelins (SMs) containing homogeneous acyl chains
with 12, 14, 16, 18, 24, or 26 carbons were synthesized and
characterized using an automated Langmuir-type film balance. Surface
pressure was monitored as a function of lipid molecular area at
constant temperatures between 10°C and 30°C. SM containing lauroyl
(12:0) acyl chains displayed only liquid-expanded behavior. Increasing the length of the saturated acyl chain (e.g., 14:0, 16:0, or 18:0) resulted in liquid-expanded to condensed two-dimensional phase transitions at many temperatures in the 10-30°C range. Similar behavior was observed for SMs with lignoceroyl (24:0) or (cerotoyl) 26:0 acyl chains, but isotherms showed only condensed behavior at 10 and 15°C. Insights into the physico-mechanical in-plane interactions
occurring within the different SM phases and accompanying changes in SM
phase state were provided by analyzing the interfacial area
compressibility moduli. At similar surface pressures, SM fluid phases
were less compressible than those of phosphatidylcholines with similar
chain structures. The area per molecule and compressibility of SM
condensed phases depended upon the length of the saturated acyl chain
and upon spreading temperature. Spreading of SMs with very long
saturated acyl chains at temperatures 30-35° below
Tm resulted in condensed films with lower
in-plane compressibilities, but consistently larger cross-sectional
molecular areas than the condensed phases achieved by spreading at
temperatures only 10-20° below Tm. This
behavior is discussed in terms of the enhancement of SM lateral
aggregation by temperature reduction, a common approach used during
domain isolation from biomembranes.
Biophys J, April 2000, p. 1921-1931, Vol. 78, No. 4
© 2000 by the Biophysical Society 0006-3495/00/04/1921/11 $2.00
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