Literature DB >> 7893682

Evidence for transbilayer, tail-to-tail cholesterol dimers in dipalmitoylglycerophosphocholine liposomes.

J S Harris1, D E Epps, S R Davio, F J Kézdy.   

Abstract

The behavior of multilamellar liposomes of 2,3-dipalmitoyl-sn-glycero-1-phosphocholine (DPPC) was studied by differential scanning calorimetry (DSC) in the presence of < or = 5 mol % of the amphiphilic solutes methyl oleate, cholesterol, pregnenolone, and dehydroandrosterone. The DSC thermograms indicate that the solutes are miscible only with the liquid-disordered (Id) phase, and not with the solid-ordered (so) phase. The slopes of the Tm vs solute concentration curves confirm this conclusion: It appears that the so-1d phase transition of DPPC, which corresponds to the melting of the phospholipid chains, can be treated as a simple melting process and, thus, could be used as a cryoscopic system. In that case, its melting point depression constant, Kf, can be calculated a priori from the experimentally measured heat of fusion per gram of DPPC, lf, and the temperature of the phase transition of pure DPPC, T(o), by the equation Kf = RTo2/(1000lf) = 12.3 +/- 0.9 K g M-1 cm3. With methyl oleate as the solute, the Tm vs methyl oleate concentration plot is linear, and from the slope we calculate Kf = 12.9 +/- 0.8 K g M-1 cm3. Thus, methyl oleate appears to form an ideal cryoscopic system with dipalmitoyllecithin liposomes: It is fully miscible with the 1d phase but is apparently insoluble in the s(o) phase. Pregnenolone and dehydroandrosterone also form ideal cryoscopic systems with dipalmitoyllecithin liposomes: The Tm vs solute concentration plots are linear and yield the correct MWs for these solutes.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7893682     DOI: 10.1021/bi00011a043

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  23 in total

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Authors:  Susana A Sánchez; M Alejandra Tricerri; Giulia Ossato; Enrico Gratton
Journal:  Biochim Biophys Acta       Date:  2010-03-27

2.  Control of lipid membrane stability by cholesterol content.

Authors:  S Raffy; J Teissié
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

3.  Cholesterol organization in membranes at low concentrations: effects of curvature stress and membrane thickness.

Authors:  R Rukmini; S S Rawat; S C Biswas; A Chattopadhyay
Journal:  Biophys J       Date:  2001-10       Impact factor: 4.033

4.  Exploring the structure and stability of cholesterol dimer formation in multicomponent lipid bilayers.

Authors:  Asanga Bandara; Afra Panahi; George A Pantelopulos; John E Straub
Journal:  J Comput Chem       Date:  2016-10-20       Impact factor: 3.376

5.  Methyl-β-cyclodextrins preferentially remove cholesterol from the liquid disordered phase in giant unilamellar vesicles.

Authors:  Susana A Sanchez; German Gunther; Maria A Tricerri; Enrico Gratton
Journal:  J Membr Biol       Date:  2011-04-06       Impact factor: 1.843

6.  Rapid transbilayer movement of the fluorescent sterol dehydroergosterol in lipid membranes.

Authors:  Karin John; Janek Kubelt; Peter Müller; Daniel Wüstner; Andreas Herrmann
Journal:  Biophys J       Date:  2002-09       Impact factor: 4.033

7.  Membrane fluidity and lipid order in ternary giant unilamellar vesicles using a new bodipy-cholesterol derivative.

Authors:  Florly S Ariola; Zaiguo Li; Christine Cornejo; Robert Bittman; Ahmed A Heikal
Journal:  Biophys J       Date:  2009-04-08       Impact factor: 4.033

8.  Cholesterol distribution in living cells: fluorescence imaging using dehydroergosterol as a fluorescent cholesterol analog.

Authors:  S Mukherjee; X Zha; I Tabas; F R Maxfield
Journal:  Biophys J       Date:  1998-10       Impact factor: 4.033

9.  Cholesterol-induced interfacial area condensations of galactosylceramides and sphingomyelins with identical acyl chains.

Authors:  J M Smaby; M Momsen; V S Kulkarni; R E Brown
Journal:  Biochemistry       Date:  1996-05-07       Impact factor: 3.162

10.  The insertion and transport of anandamide in synthetic lipid membranes are both cholesterol-dependent.

Authors:  Eric Di Pasquale; Henri Chahinian; Patrick Sanchez; Jacques Fantini
Journal:  PLoS One       Date:  2009-03-30       Impact factor: 3.240

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