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Literature DB >> 1911829

Epifluorescence microscopic observation of monolayers of dipalmitoylphosphatidylcholine: dependence of domain size on compression rates.

Abstract

A fluorescence microscopic technique was used to observe phase transitions in monolayers of DPPC. The sizes of the domain structures observed were found to be dependent on the rate of compression of the monolayer. The distribution of domain sizes for different rates of compression were unimodal, but the scatter in the sizes was greater during slow compressions.

Entities: Chemical

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Year: 1991 PMID： 1911829 DOI： 10.1016/0005-2736(91)90204-l

Source DB: PubMed Journal: Biochim Biophys Acta ISSN： 0006-3002

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Cited

22 in total

1. Differential effects of surfactant protein A on regional organization of phospholipid monolayers containing surfactant protein B or C.

Authors: S G Taneva; K M Keough
Journal: Biophys J Date: 2000-10 Impact factor: 4.033

2. Effect of pulmonary surfactant protein SP-B on the micro- and nanostructure of phospholipid films.

Authors: Antonio Cruz; Luis Vázquez; Marisela Vélez; Jesús Pérez-Gil
Journal: Biophys J Date: 2004-01 Impact factor: 4.033

3. Fluorescence, polarized fluorescence, and Brewster angle microscopy of palmitic acid and lung surfactant protein B monolayers.

Authors: M M Lipp; K Y Lee; A Waring; J A Zasadzinski
Journal: Biophys J Date: 1997-06 Impact factor: 4.033

9. Determination of fluid and gel domain sizes in two-component, two-phase lipid bilayers. An electron spin resonance spin label study.

Authors: M B Sankaram; D Marsh; T E Thompson
Journal: Biophys J Date: 1992-08 Impact factor: 4.033

10. Aggregation of puroindoline in phospholipid monolayers spread at the air-liquid interface.

Authors: L Dubreil; V Vié; S Beaufils; D Marion; A Renault
Journal: Biophys J Date: 2003-10 Impact factor: 4.033

Epifluorescence microscopic observation of monolayers of dipalmitoylphosphatidylcholine: dependence of domain size on compression rates.

1. Differential effects of surfactant protein A on regional organization of phospholipid monolayers containing surfactant protein B or C.

2. Effect of pulmonary surfactant protein SP-B on the micro- and nanostructure of phospholipid films.

3. Fluorescence, polarized fluorescence, and Brewster angle microscopy of palmitic acid and lung surfactant protein B monolayers.

4. Spontaneous formation of interfacial lipid-protein monolayers during adsorption from vesicles.

5. Estimation of hemosiderosis in seabirds and fish exposed to petroleum.

6. IR spectroscopic determination of gel state miscibility in long-chain phosphatidylcholine mixtures.

7. Pulmonary surfactant protein A interacts with gel-like regions in monolayers of pulmonary surfactant lipid extract.

8. Comparison of Line Tension Measurement Methods for Lipid Monolayers at Liquid-Liquid Coexistence.

9. Determination of fluid and gel domain sizes in two-component, two-phase lipid bilayers. An electron spin resonance spin label study.

10. Aggregation of puroindoline in phospholipid monolayers spread at the air-liquid interface.