THE INFLUENCE OF HYDROPHOBIC MISMATCH ON ANDROSTEROL PHOSPHATIDYLCHOLINE INTERACTIONS IN MODEL MEMBRANES/

Citation
H. Ohvorekila et al., THE INFLUENCE OF HYDROPHOBIC MISMATCH ON ANDROSTEROL PHOSPHATIDYLCHOLINE INTERACTIONS IN MODEL MEMBRANES/, Biochimica et biophysica acta. Biomembranes, 1372(2), 1998, pp. 331-338
Citations number
36
Categorie Soggetti
Biology,Biophysics
ISSN journal
00052736
Volume
1372
Issue
2
Year of publication
1998
Pages
331 - 338
Database
ISI
SICI code
0005-2736(1998)1372:2<331:TIOHMO>2.0.ZU;2-Z
Abstract
We have examined the association of 5-androsten-3 beta-ol (androsterol ) with saturated phosphatidylcholines (PCs), having symmetric acyl cha ins from 10 to 16 carbons in length, in both mono- and bilayer membran es. The emphasis of the study was to measure how hydrophobic mismatch (i.e. the difference in hydrophobic length of the interacting molecule s) affected androsterol/PC interactions in model membranes. With monol ayer membranes (33 mol% sterol, 20 mN/m, 25 degrees C), androsterol wa s found to be macroscopically miscible with all the tested PCs. Andros terol was observed to condense the lateral packing of di14 and di15 PC s (by 6 and 4.5 A(2) per molecule, respectively), but failed to conden se shorter (di10, di11, di12 and di13 PCs) or the longer chain di16PC. The rate of androsterol desorption from mixed monolayers to P-cyclode xtrin accepters in the subphase was a clear function of the host PC ac yl chain length. The slowest rate of androsterol desorption (i.e. best androsterol/PC interaction) was seen from a di14PC monolayer, whereas the desorption rate increased when the host PC had shorter or longer chains. When the cholesterol oxidase susceptibility of androsterol was determined in small unilamellar vesicles (SW) containing PCs of diffe rent chain lengths (33 mol% androsterol), the slowest rate of oxidatio n was seen in di14PC vesicles, whereas higher rates were measured for shorter or longer chain PC vesicles, again suggesting that androsterol interacted more favorably with di14PC than with the other PCs. In con clusion, the hydrophobic mismatch between androsterol and different PC s appeared to greatly affect the intermolecular interactions, as deter mined from the condensation effect, from sterol desorption rates, and the oxidation susceptibility of androsterol. Although androsterol is n ot a physiological membrane component, the present model system clearl y shows that hydrophobic mismatch has a great influence on how sterols and phosphatidylcholines interact in membranes. (C) 1998 Elsevier Sci ence B.V. All rights reserved.