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In vitro determination of the solubility limit of cholesterol in phospholipid bilayers
被引:9
|作者:
Epand, Richard M.
[1
]
Bach, Diana
[2
]
Wachtel, Ellen
[3
]
机构:
[1] McMaster Univ, Dept Biochem, Hamilton, ON L8S 4K1, Canada
[2] Weizmann Inst Sci, Dept Biomol Sci, Rehovot, Israel
[3] Weizmann Inst Sci, Fac Chem, Rehovot, Israel
关键词:
Cholesterol;
Cholesterol crystals;
THERMOTROPIC PHASE-BEHAVIOR;
MODEL ORGANIC-COMPOUNDS;
RAPID SOLVENT EXCHANGE;
SPINNING NMR-SPECTRA;
CRYSTAL-STRUCTURE;
CROSS-POLARIZATION;
MEMBRANES;
MIXTURES;
PHOSPHATIDYLSERINE;
PHOSPHATIDYLCHOLINE;
D O I:
10.1016/j.chemphyslip.2016.06.006
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Cholesterol has limited solubility in phospholipid bilayers. The solubility limit is strongly dependent on the nature of the lipid with which the cholesterol is mixed while properties of the crystals formed can be modified by phospholipid-cholesterol interactions. In this review we summarize the various methods that have been developed to prepare hydrated mixtures of cholesterol and phospholipid. We point out some of the factors that determine the form adopted when cholesterol crystallizes in such mixtures, i.e. two- or three-dimensional, monohydrate or anhydrous. These differences can greatly affect the ability to experimentally detect the presence of these crystals in a membrane. Several methods for detecting cholesterol crystals are discussed and compared including DSC, X-ray and GIXRD diffraction methods, NMR and EPR spectroscopy. The importance of the history of the sample in determining the amount and nature of the cholesterol crystals formed is emphasized. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
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页码:3 / 10
页数:8
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