scholarly journals Interactions of tocopherols and ubiquinones with monolayers of phospholipids

1977 ◽  
Vol 161 (1) ◽  
pp. 111-121 ◽  
Author(s):  
B Maggio ◽  
A T Diplock ◽  
J A Lucy

1. The penetration of alpha-tocopherol and seven of its derivatives, and five compounds in the ubiquinone series, having differing chain lengths, into monolayers at the air/water interface of 11 different synthetic phospholipids and cholesterol was investigated; the properties of mixed monolayers of the tocopherols and of ubiquinones with phospholipids were also studied. 2. Penetration of alpha-tocopherol into diarachidonylglycerylphosphorycholine was approximately constant for molar ratios of tocopherol/phospholipid ranging from 0.4:1.0 to 2.0:1.0. 3. Tocopherols with shorter or longer side chains than alpha-tocopherol had a lesser ability to penetrate monolayers of phospholipid molecules with 16 or more carbon atoms in their acyl chains. 4. All the tocopherols penetrated more readily as unsaturation in the phospholipids was increased, and their penetration into mixed monolayers of phospholipids was greatly facilitated by the presence of relatively small quantities of unsaturated phospholipid molecules. 5. There was relatively little interaction between the tocopherols and cholesterol, or between the ubiquinones and phospholipids. 6. The possible significance of the observed interactions between alpha-tocopherol and polyunsaturated phospholipids is discussed in relation to the biochemical actions of alpha-tocopherol in vivo. 7. It is suggested that fluidity of the lipid bilayer in membranes containing polyunsaturated phospholipids may allow alpha-tocopherol to interact in a dynamic manner with a number of phospholipid molecules.

Langmuir ◽  
2000 ◽  
Vol 16 (17) ◽  
pp. 7051-7055 ◽  
Author(s):  
Jian Bang Peng ◽  
Gwen A. Lawrie ◽  
Geoffrey T. Barnes ◽  
Ian R. Gentle ◽  
Garry J. Foran ◽  
...  

Biochimie ◽  
2009 ◽  
Vol 91 (6) ◽  
pp. 765-773 ◽  
Author(s):  
Sabine Castano ◽  
Brigitte Delord ◽  
Annie Février ◽  
Jean-Marie Lehn ◽  
Pierre Lehn ◽  
...  

Langmuir ◽  
1999 ◽  
Vol 15 (2) ◽  
pp. 600-606 ◽  
Author(s):  
Keiji Tanaka ◽  
Patricia A. Manning ◽  
Victor K. Lau ◽  
Hyuk Yu

1995 ◽  
Vol 269 (4) ◽  
pp. L492-L497 ◽  
Author(s):  
T. M. McEachren ◽  
K. M. Keough

The influence of the acute inflammatory phase protein human C-reactive protein (CRP) on the adsorption of porcine pulmonary surfactant from a subphase into an air-water interface has been investigated. CRP was shown to detract from the ability of surfactant to rapidly adsorb to the air-water interface at a molar ratio of 0.03:1 (protein:phospholipid) (weight ratio, 0.5:1). On a weight basis, CRP was found to be more effective than fibrinogen at reducing the adsorption rate of surfactant. The effect of CRP required the presence of calcium and was reversed by the addition of phosphocholine in a concentration-dependent manner. The inhibition of surfactant adsorption by CRP was effectively eliminated by the addition of phosphocholine at a molar ratio of 300:1 (phosphocholine:CRP), but it was not diminished by the addition of identical molar ratios of o-phosphoethanolamine or DL-alpha-glycerophosphate at the same molar ratios. These data suggest that the potent inhibition of surfactant adsorption by CRP is primarily a result of a specific interaction between CRP and the phosphocholine headgroup of surfactant lipids in the subphase and that it can be reversed by the water-soluble CRP ligand, phosphocholine.


2002 ◽  
Vol 4 (11) ◽  
pp. 2329-2336 ◽  
Author(s):  
José M. Pedrosa ◽  
Marta Pérez ◽  
Inmaculada Prieto ◽  
María Teresa Martín-Romero ◽  
Dietmar Möbius ◽  
...  

2008 ◽  
Vol 327 (1) ◽  
pp. 162-168 ◽  
Author(s):  
Rong Li ◽  
Qibin Chen ◽  
Dazhi Zhang ◽  
Honglai Liu ◽  
Ying Hu

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