A modified squeeze-out mechanism for generating high surface pressures with pulmonary surfactant

Pulmonary surfactant stabilizes the alveoli by lining the air-fluid interface with films that reduce surface tension to near 0 mN/m (γmin). Surfactant protein B (SP-B) enhances the surface activity of surfactant phospholipids. A captive bubble tensiometer (CBT) was used to study the properties of adsorbed films of dipalmitoylphosphatidylcholine (DPPC) with acidic 1-palmitoyl-2-oleoyl- sn-glycero-3-[phospho- rac-(1-glycerol)] (POPG) or neutral 1-palmitoyl-2-oleoyl- sn-glycerol-3-phosphocholine with (7:3) and without 1% dimeric SP-B. SP-B enhanced the adsorption rate of DPPC-containing neutral or acidic lipid suspensions (1 mg/ml) to a similar extent. Quasi-static cycling of these films revealed that SP-B significantly decreased the film area reduction required to reach γmin for the acidic but not for the neutral system. The results obtained with DPPC-phosphatidylglycerol (PG)-SP-B were consistent with selective DPPC adsorption into the surface monolayer during film formation. Film area reduction required to reach γmin with this system (with and without calcium) approached that of pure DPPC, suggesting selective DPPC insertion and PG squeeze-out. Dynamic cycling of such films showed that larger film area reductions were required to reach γmin for the neutral than for acidic system, even after 20 cycles. Fluorescence microscopy of solvent-spread DPPC-POPG-SP-B planar films revealed highly condensed structures at ∼25 mN/m, although no specific PG phase-segregated structures could be identified. The study suggests that specific interactions of SP-B with acidic phospholipids of surfactant may be involved in the generation and maintenance of DPPC-rich films in the alveoli.

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Effect of pulmonary surfactant protein B (SP-B) and calcium on phospholipid adsorption and squeeze-out of phosphatidylglycerol from binary phospholipid monolayers containing dipalmitoylphosphatidylcholine

Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism ◽

10.1016/0005-2760(92)90212-e ◽

1992 ◽

Vol 1126 (1) ◽

pp. 26-34 ◽

Cited By ~ 50

Author(s):

Shou-Hwa Yu ◽

Fred Possmayer

Keyword(s):

Pulmonary Surfactant ◽

Surfactant Protein ◽

Phospholipid Monolayers ◽

Surfactant Protein B ◽

Squeeze Out ◽

Pulmonary Surfactant Protein B ◽

Pulmonary Surfactant Protein ◽

Protein B

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Pulmonary Surfactant Reduces Surface Tension to Low Values near Zero through a Modified Squeeze-Out Mechanism

Biophysical Journal ◽

10.1016/j.bpj.2011.11.2263 ◽

2012 ◽

Vol 102 (3) ◽

pp. 414a

Author(s):

Fred Possmayer ◽

Nora Keating ◽

Yi Y. Zuo ◽

Nils O. Petersen ◽

Ruud A. Veldhuizen

Keyword(s):

Surface Tension ◽

Pulmonary Surfactant ◽

Squeeze Out

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Localization of Adenosine Triphosphatase Activity in the Phleom of Nicotiana Tabacum

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100094401 ◽

1972 ◽

Vol 30 ◽

pp. 230-231

Author(s):

James Cronshaw ◽

Jamison E. Gilder

Keyword(s):

Plasma Membrane ◽

Atpase Activity ◽

Adenosine Triphosphatase ◽

Higher Plants ◽

High Surface ◽

Root Tip ◽

Animal Cells ◽

Physiological Processes ◽

Tip Cells ◽

Atpase Localization

Adenosine triphosphatase (ATPase) activity has been shown to be associated with numerous physiological processes in both plants and animal cells. Biochemical studies have shown that in higher plants ATPase activity is high in cell wall preparations and is associated with the plasma membrane, nuclei, mitochondria, chloroplasts and lysosomes. However, there have been only a few ATPase localization studies of higher plants at the electron microscope level. Poux (1967) demonstrated ATPase activity associated with most cellular organelles in the protoderm cells of Cucumis roots. Hall (1971) has demonstrated ATPase activity in root tip cells of Zea mays. There was high surface activity largely associated with the plasma membrane and plasmodesmata. ATPase activity was also demonstrated in mitochondria, dictyosomes, endoplasmic reticulum and plastids.

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In Situ microscopy of the anodic etching of silicon

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100137537 ◽

1995 ◽

Vol 53 ◽

pp. 232-233

Author(s):

Frances M. Ross ◽

Peter C. Searson

Keyword(s):

Composite Structures ◽

High Surface ◽

High Surface Area ◽

Chemical Properties ◽

Selective Etching ◽

Silicon On Insulator ◽

Second Phase ◽

Porous Layers ◽

New Class ◽

Porous Semiconductors

Porous semiconductors represent a relatively new class of materials formed by the selective etching of a single or polycrystalline substrate. Although porous silicon has received considerable attention due to its novel optical properties1, porous layers can be formed in other semiconductors such as GaAs and GaP. These materials are characterised by very high surface area and by electrical, optical and chemical properties that may differ considerably from bulk. The properties depend on the pore morphology, which can be controlled by adjusting the processing conditions and the dopant concentration. A number of novel structures can be fabricated using selective etching. For example, self-supporting membranes can be made by growing pores through a wafer, films with modulated pore structure can be fabricated by varying the applied potential during growth, composite structures can be prepared by depositing a second phase into the pores and silicon-on-insulator structures can be formed by oxidising a buried porous layer. In all these applications the ability to grow nanostructures controllably is critical.

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Diffraction from arrays of antiphase boundaries in ordered III-V alloys

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100126378 ◽

1987 ◽

Vol 45 ◽

pp. 312-313

Author(s):

T. S. Kuan

Keyword(s):

High Surface ◽

Growth Conditions ◽

Ternary Alloys ◽

Local Growth ◽

Antiphase Boundaries ◽

Surface Mobility ◽

Ordered Phases ◽

Diffraction Patterns ◽

Atomically Flat ◽

Degree Of Order

Recent electron diffraction studies have found ordered phases in AlxGa1-xAs, GaAsxSb1-x, and InxGa1-xAs alloy systems, and these ordered phases are likely to be found in many other III-V ternary alloys as well. The presence of ordered phases in these alloys was detected in the diffraction patterns through the appearance of superstructure reflections between the Bragg peaks (Fig. 1). The ordered phase observed in the AlxGa1-xAs and InxGa1-xAs systems is of the CuAu-I type, whereas in GaAsxSb1-x this phase and a chalcopyrite type ordered phase can be present simultaneously. The degree of order in these alloys is strongly dependent on the growth conditions, and during the growth of these alloys, high surface mobility of the depositing species is essential for the onset of ordering. Thus, the growth on atomically flat (110) surfaces usually produces much stronger ordering than the growth on (100) surfaces. The degree of order is also affected by the presence of antiphase boundaries (APBs) in the ordered phase. As shown in Fig. 2(a), a perfectly ordered In0.5Ga0.5As structure grown along the <110> direction consists of alternating InAs and GaAs monolayers, but due to local growth fluctuations, two types of APBs can occur: one involves two consecutive InAs monolayers and the other involves two consecutive GaAs monolayers.

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Electron holography of catalysts

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100138452 ◽

1995 ◽

Vol 53 ◽

pp. 416-417

Author(s):

A. K. Datye ◽

D. S. Kalakkad ◽

L. F. Allard ◽

E. Völkl

Keyword(s):

Heterogeneous Catalysts ◽

High Surface ◽

High Surface Area ◽

Atomic Scale ◽

Nano Particles ◽

Phase Image ◽

Electron Holography ◽

Specimen Thickness ◽

Phase Information ◽

Particle Structure

The active phase in heterogeneous catalysts consists of nanometer-sized metal or oxide particles dispersed within the tortuous pore structure of a high surface area matrix. Such catalysts are extensively used for controlling emissions from automobile exhausts or in industrial processes such as the refining of crude oil to produce gasoline. The morphology of these nano-particles is of great interest to catalytic chemists since it affects the activity and selectivity for a class of reactions known as structure-sensitive reactions. In this paper, we describe some of the challenges in the study of heterogeneous catalysts, and provide examples of how electron holography can help in extracting details of particle structure and morphology on an atomic scale.Conventional high-resolution TEM imaging methods permit the image intensity to be recorded, but the phase information in the complex image wave is lost. However, it is the phase information which is sensitive at the atomic scale to changes in specimen thickness and composition, and thus analysis of the phase image can yield important information on morphological details at the nanometer level.

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Structure and composition of metal particles in Pt-Sn/Al2O3 bimetallic catalysts

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100174527 ◽

1990 ◽

Vol 48 (4) ◽

pp. 278-279

Author(s):

A. Sachdev ◽

J. Schwank

Keyword(s):

Bimetallic Catalysts ◽

Bimetallic Catalyst ◽

Size Structure ◽

High Surface ◽

High Surface Area ◽

Metal Particles ◽

Alloy Formation ◽

Particle Size Range ◽

Oxide Supports ◽

Petroleum Fractions

Platinum - tin bimetallic catalysts have been primarily utilized in the chemical industry in the catalytic reforming of petroleum fractions. In this process the naphtha feedstock is converted to hydrocarbons with higher octane numbers and high anti-knock qualities. Most of these catalysts contain small metal particles or crystallites supported on high surface area insulating oxide supports. The determination of the structure and composition of these particles is crucial to the understanding of the catalytic behavior. In a bimetallic catalyst it is important to know how the two metals are distributed within the particle size range and in what way the addition of a second metal affects the size, structure and composition of the metal particles. An added complication in the Pt-Sn system is the possibility of alloy formation between the two elements for all atomic ratios.

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