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R E Barnett

Publications and source records attributed to R E Barnett.

16 recordsLinked to original sources

Lack of transbilayer coupling in phase transitions of phosphatidylcholine vesicles.

Praseodymium and ytterbium chlorides were used as nuclear magnetic resonance shift reagents to resolve the inner and outer choline methyl resonances of single-walled dimyristoylphosphatidylcholine bilayer vesicles. The gel to liquid-crystalline phase transition of these vesicles was monitored by observing the proton and carbon-13 nuclear magnetic resonance line widths of the choline methyl group nuclei. In the absence of ions the transition occurred at 21.5 degrees C in both halves of the bilayer. With Pr3+ or Yb3+ added to the outside of the vesicles, the phase transition temperature of the outer half of the bilayer was raised several degrees, while the transition temperature of the inner half was unchanged. In vesicles containing 20 mol % cholesterol the phase transition of the outer monolayer was considerably broadened, while the inner half still melted sharply at 21.6 degrees C. By use of dipalmitoylphosphatidylcholine vesicles with UO2(2)+ added to the outside, phase transitions at 41.5 and 44 degrees C were detected by electron spin resonance with the spin-label 2,2,6,6-tetramethylpiperidinyl-l-oxy. These results imply that the two halves of the bilayer in phospholipid vesicles are so weakly coupled that they can undergo the gel to liquid-crystalline phase transition independently.

Dimyristoylphosphatidylcholine↗

Magnetic resonance study of the distribution of 2,2,6,6-tetramethylpiperidine-N-oxyl in phosphatidylcholine bilayers.

With the aid of paramagentic praseodymium ions the resonances at 60 MHz of the inward and outward facing choline methyl protons of sonicated egg yolk phosphatidylcholine vesicles were resolved. The subsequent addition of 2,2,6,6,-tetramethylpiperidine-N-oxyl (TEMPO) to the vesicle suspension broadened the inner and outer resonances equally. TEMPO easily penetrates the egg yolk phosphatidylcholine vesicles and has free access to the entire lipid volume above the gel to liquid crystalline transition temperature. The electron spin resonance (ESR) spectrum of TEMPO in the egg yolk phosphatidylcholine suspension exhibits features indicating that TEMPO dissolves principally in the hydrocarbon portion of the egg yolk phosphatidylcholine bilayer. The egg yolk phosphatidylcholine methylene chain proton resonances are also broadened by TEMPO notably to a greater extent than the choline methyl resonances. These data indicate that TEMPO should be more sensitive to the melting behavior of the fatty acyl chains of phospholipid suspensions than to the polar head groups.

Cyclic N-Oxides↗

Differences in membrane fluidity and structure in contact-inhibited and transformed cells.

Studies on contact-inhibited mouse embryo fibroblast 3T3 cells and 3T3 cells transformed by oncogenic RNA and DNA viruses and by a chemical carcinogen have demonstrated differences in plasma membrane architecture. Spin-label and freeze-fracture ultrastructural studies have shown that contact-inhibited cells have ordered membrane lipids and aggregated intramembranous particles, whereas transformed cells have fluid membrane lipids and randomly distributed intramembranous particles. These findings suggest a model for how changes in the cell membrane may account for some of the characteristic differences observed between contact-inhibited and transformed cells.

Animals↗