Cholesterol modifies the properties of surface films of dipalmitoylphosphatidylcholine plus pulmonary surfactant-associated protein B or C spread or adsorbed at the air-water interface
- PMID: 9020791
- DOI: 10.1021/bi9623542
Cholesterol modifies the properties of surface films of dipalmitoylphosphatidylcholine plus pulmonary surfactant-associated protein B or C spread or adsorbed at the air-water interface
Abstract
Cholesterol is a substantial component of pulmonary surfactant (approximately 8 wt % or approximately 14 mol % of surfactant lipids). This study investigated the effect of cholesterol on the way in which hydrophobic SP-B and SP-C modulated the adsorption of lipid into the air-water interface and their respreading from collapsed phase produced on overcompression of the surface film. The properties of binary spread monolayers of SP-B or SP-C plus cholesterol (CH) were consistent with miscibility between the hydrophobic proteins and the sterol. Results from surface pressure versus area measurements at 23 degrees C on spread monolayers of dipalmitoylphosphatidylcholine (DPPC) plus SP-B in the presence of 8 wt % cholesterol implied that CH did not significantly affect the properties of the films of SP-B/(DPPC/CH) compared to those of binary SP-B/DPPC monolayers. In contrast, CH appeared to enhance the mixing of SP-C with DPPC/CH in ternary SP-C/(DPPC/CH) films compared to the miscibility of SP-C with DPPC in the SP-C/DPPC films. It is estimated that about 10 wt % SP-C might remain in the SP-C/(DPPC/CH) monolayers compressed to high surface pressures of about 72 mN/m, whereas SP-C at concentrations of > or = 5 wt % was squeezed out at pi approximately 50 mN/m from SP-C/DPPC films without cholesterol. Cholesterol reduced the stability of the films of SP-B/(DPPC/CH) and SP-C/(DPPC/CH) when they had been compressed to pi approximately 72 mN/m, in contrast to films of SP-B/DPPC and SP-C/DPPC which exhibited a relatively slow relaxation from the collapse pressure of 72 mN/m. Dynamic cyclic compression beyond collapse of SP-B/(DPPC/CH) and SP-C/(DPPC/CH) monolayers showed that cholesterol diminished their postcollapse respreading compared to the respreading of the protein/DPPC films without cholesterol. Cholesterol, at 8 wt %, inhibited the rate of adsorption to the air-water interface at 35 degrees C of aqueous dispersions of DPPC containing 2.5 or 5 wt % SP-B or SP-C. The results suggest that cholesterol has an apparent negative influence on the surfactant surface properties, which are generally considered to be important in surfactant function, although increasing protein concentrations can counteract some of the negative influences.
Similar articles
-
Pulmonary surfactant proteins SP-B and SP-C in spread monolayers at the air-water interface: III. Proteins SP-B plus SP-C with phospholipids in spread monolayers.Biophys J. 1994 Apr;66(4):1158-66. doi: 10.1016/S0006-3495(94)80897-5. Biophys J. 1994. PMID: 8038387 Free PMC article.
-
Pulmonary surfactant protein SP-A with phospholipids in spread monolayers at the air-water interface.Biochemistry. 1995 Aug 15;34(32):10279-89. doi: 10.1021/bi00032a023. Biochemistry. 1995. PMID: 7640284
-
Hysteresis behavior of amphiphilic model peptide in lung lipid monolayers at the air-water interface by an IRRAS measurement.Colloids Surf B Biointerfaces. 2009 Jan 1;68(1):61-7. doi: 10.1016/j.colsurfb.2008.09.013. Epub 2008 Sep 21. Colloids Surf B Biointerfaces. 2009. PMID: 18977123
-
New insights into lung surfactant monolayers using vibrational sum frequency generation spectroscopy.Photochem Photobiol. 2006 Nov-Dec;82(6):1517-29. doi: 10.1562/2006-06-30-IR-958. Photochem Photobiol. 2006. PMID: 16930094 Review.
-
Interfacial properties of pulmonary surfactant layers.Adv Colloid Interface Sci. 2005 Dec 14;117(1-3):33-58. doi: 10.1016/j.cis.2005.05.001. Epub 2005 Aug 24. Adv Colloid Interface Sci. 2005. PMID: 16120435 Review.
Cited by
-
Physical properties of phospholipids and integral proteins and their biofunctional roles in pulmonary surfactant from molecular dynamics simulation.RSC Adv. 2020 Feb 27;10(14):8568-8579. doi: 10.1039/d0ra00077a. eCollection 2020 Feb 24. RSC Adv. 2020. PMID: 35497816 Free PMC article.
-
Combined effect of synthetic protein, Mini-B, and cholesterol on a model lung surfactant mixture at the air-water interface.Biochim Biophys Acta. 2016 Apr;1858(4):904-12. doi: 10.1016/j.bbamem.2016.01.008. Epub 2016 Jan 15. Biochim Biophys Acta. 2016. PMID: 26775740 Free PMC article.
-
The role of surfactant proteins in DPPC enrichment of surface films.Biophys J. 2000 Dec;79(6):3164-71. doi: 10.1016/S0006-3495(00)76550-7. Biophys J. 2000. PMID: 11106621 Free PMC article.
-
Palmitoylation of pulmonary surfactant protein SP-C is critical for its functional cooperation with SP-B to sustain compression/expansion dynamics in cholesterol-containing surfactant films.Biophys J. 2010 Nov 17;99(10):3234-43. doi: 10.1016/j.bpj.2010.08.070. Biophys J. 2010. PMID: 21081071 Free PMC article.
-
Multilayer structures in lipid monolayer films containing surfactant protein C: effects of cholesterol and POPE.Biophys J. 2005 Apr;88(4):2638-49. doi: 10.1529/biophysj.104.050823. Epub 2005 Jan 14. Biophys J. 2005. PMID: 15653721 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous