Effect of sugars and dimethyl sulfoxide on the structure and phase behavior of DPPC monolayers

Citation
N. Krasteva et al., Effect of sugars and dimethyl sulfoxide on the structure and phase behavior of DPPC monolayers, LANGMUIR, 17(4), 2001, pp. 1209-1214
Citations number
44
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
17
Issue
4
Year of publication
2001
Pages
1209 - 1214
Database
ISI
SICI code
0743-7463(20010220)17:4<1209:EOSADS>2.0.ZU;2-#
Abstract
Sugars accumulate in the tissues of some organisms, preventing cell damage during freezing and desiccation. Dimethyl sulfoxide (DMSO) is an artificial membrane cryoprotector, but in some cases it destabilizes the membranes an d promotes their fusion and leakage. Insoluble dipalmitoyl phosphatidylchol ine (DPPC) monolayers spread on sugar or DMSO-containing subphases are used to study the interactions of the soluble sugars and DMSO with the main mem brane phospholipid. The monolayer phase behavior was studied by means of pr essure-area isotherms and grazing incidence X ray diffraction. The addition of sugars in the subphase increases the mean molecular area of the DPPC mo lecules in the fluid phase. The expanding effect increases with the sugar c oncentration and is more pronounced if sucrose is used instead of fructose. The formation of the DPPC condensed phase occurs at slightly higher surfac e pressures on sugar solutions, but the structure of the condensed phase is not influenced by the sugars. At low surface pressures, the sugar molecule s penetrate into the polar headgroup region of the lipid monolayer. At high lateral pressure, they are squeezed out from the monolayer. In contrast, t he addition of DMSO causes condensation of the monolayer and decrease of th e transition pressure from the expanded to the condensed phase. At a certai n DMSO concentration, condensed phase formation is observed at zero surface pressure. The presence of DMSO in the subphase causes shrinkage of the alk yl chain lattice and a decrease in the tilt angle of the DPPC molecules. Th e observed effect is attributed to a reduced hydration of the DPPC molecule s, which causes a decrease in the headgroup repulsion and facilitates the a ttraction between the lipid alkyl chains.