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1.
Langmuir ; 30(12): 3285-9, 2014 Apr 01.
Article in English | MEDLINE | ID: mdl-24621400

ABSTRACT

A quantitative assessment has been made of the interaction between exchangeable mimics of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and cholesterol in the liquid-ordered (l0) and the liquid-disordered (ld) states using the nearest-neighbor recognition (NNR) method. This assessment has established that these lipids mix ideally in the l0 phase (i.e., they show no net attraction or repulsion toward each other) but exhibit repulsive interactions in the ld phase. The implications of these findings for the interactions between unsaturated phospholipids and cholesterol in eukaryotic cell membranes are briefly discussed.


Subject(s)
Cholesterol/chemistry , Membrane Microdomains/chemistry , Phosphatidylcholines/chemistry , Cell Membrane/chemistry , Eukaryotic Cells/chemistry , Molecular Structure
2.
J Am Chem Soc ; 134(41): 17245-52, 2012 Oct 17.
Article in English | MEDLINE | ID: mdl-22998217

ABSTRACT

Nearest-neighbor recognition (NNR) measurements have been made for two lipidated forms of GlyCys, interacting with analogues of cholesterol and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in the liquid-ordered (l(o)) and liquid-disordered (l(d)) phases. Interaction free energies that have been determined from these measurements have been used in Monte Carlo simulations to quantify the distribution of the peptides between liquid-ordered and liquid-disordered regions. These simulations have shown that significant differences in the lipid chains have a very weak influence on the partitioning of the peptide between these two phases. They have also revealed an insensitivity of the peptide partition coefficient, K(p), to the size of the l(o) and l(d) domains that are present. In a broader context, these findings strongly suggest that the sorting of peripheral proteins in cellular membranes via differential lipidation may be more subtle than previously thought.


Subject(s)
Lipid Bilayers/chemistry , Lipids/chemistry , Peptides/chemistry , Calorimetry, Differential Scanning , Lipids/chemical synthesis , Monte Carlo Method , Peptides/chemical synthesis
3.
Bioconjug Chem ; 23(3): 336-9, 2012 Mar 21.
Article in English | MEDLINE | ID: mdl-22372891

ABSTRACT

PEGylated phospholipids are commonly used to increase the blood-circulation time of liposomes by providing a steric barrier around them. This paper documents a fundamentally new property of these lipids-an ability to stimulate the release of cholesterol from phospholipid membranes. Evidence for such stimulation has been obtained by measuring the transport of dehydroergosterol (DHE), a fluorescent simulant of cholesterol, from donor liposomes made from 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000 (DSPE-PEG(2000)), and DHE to acceptor liposomes made from POPC, 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoglycerol (POPG), and cholesterol. The potential of PEGylated lipids to serve as novel cholesterol-lowering agents is briefly discussed.


Subject(s)
Cholesterol/chemistry , Liposomes , Membranes, Artificial , Phospholipids/chemistry , Polyethylene Glycols/chemistry
4.
Langmuir ; 27(6): 2159-61, 2011 Mar 15.
Article in English | MEDLINE | ID: mdl-21319766

ABSTRACT

The condensing effect of cholesterol on fluid bilayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine has been compared with that of dihydrocholesterol and coprostanol by means of nearest-neighbor recognition measurements. Whereas dihydrocholesterol exhibits a condensing power that is equivalent to that of cholesterol, the action of coprostanol is significantly weaker. These results provide strong support for a template mechanism of condensation and argue against an umbrella mechanism.


Subject(s)
Cholesterol/chemistry , 1,2-Dipalmitoylphosphatidylcholine/chemistry , Cholestanol/chemistry , Cholesterol/analogs & derivatives , Molecular Structure
5.
Org Lett ; 10(21): 4911-4, 2008 Nov 06.
Article in English | MEDLINE | ID: mdl-18821764

ABSTRACT

A versatile synthesis leading to either C-linked alpha- or beta-glucopyranosyl serines is presented from a common, advanced synthetic intermediate. Cyclization of the penultimate carbinol onto the alkene and methanolysis of the lactone yields selectively the alpha-linkage. A transposition of these last steps leads to the beta-linked isomer selectively.


Subject(s)
Glucose/chemistry , Serine/analogs & derivatives , Serine/chemical synthesis , Cyclization , Esterification , Molecular Structure , Serine/chemistry , Stereoisomerism
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