ArticleBiophysical journal2000
Domain growth, shapes, and topology in cationic lipid bilayers on mica by fluorescence and atomic force microscopy.
Article in Biophysical journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Interface-mediation of lipid bilayer organization and dynamics.Physical chemistry chemical physics : PCCP · 2016Article
- Toward atomic force microscopy and mass spectrometry to visualize and identify lipid rafts in plasmodesmata.Frontiers in plant science · 2014Article
- Enhancing protein stability by adsorption onto raftlike lipid domains.Journal of the American Chemical Society · 2009Article
- Effect of ions on the organization of phosphatidylcholine/phosphatidic acid bilayers.Biophysical journal · 2007Article
- Effect of surface treatment on diffusion and domain formation in supported lipid bilayers.Biophysical journal · 2007Article
- In situ scanning probe microscopy studies of tetanus toxin-membrane interactions.Biophysical journal · 2006Article
- Correlated fluorescence-atomic force microscopy of membrane domains: structure of fluorescence probes determines lipid localization.Biophysical journal · 2006Article
- Lipid asymmetry in DLPC/DSPC-supported lipid bilayers: a combined AFM and fluorescence microscopy study.Biophysical journal · 2006Article
- Correlation of AFM and SFA measurements concerning the stability of supported lipid bilayers.Biophysical journal · 2004Article
- Obstructed diffusion in phase-separated supported lipid bilayers: a combined atomic force microscopy and fluorescence recovery after photobleaching approach.Biophysical journal · 2002Article
- Spontaneous insertion and partitioning of alkaline phosphatase into model lipid rafts.EMBO reports · 2002Article
- The size of lipid rafts: an atomic force microscopy study of ganglioside GM1 domains in sphingomyelin/DOPC/cholesterol membranes.Biophysical journal · 2002Article
- Atomic force microscopy studies of ganglioside GM1 domains in phosphatidylcholine and phosphatidylcholine/cholesterol bilayers.Biophysical journal · 2001Article
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3 authors.
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Abstract
Domain formation in mica-supported cationic bilayers of dipalmitoyltrimethylammoniumpropane (DPTAP) and dimyristoyltrimethylammoniumpropane (DMTAP), fluorescently doped with an NBD (((7-nitro-2-1, 3-benzoxadiazol-4-yl)amino)caproyl) phospholipid, was investigated with fluorescence microscopy and atomic force microscopy. Heating above the acyl chain melting temperature and cooling to room temperature resulted in nucleation and growth of domains with distinguishable patterns. Fractal patterns were found for DPTAP, whereas DMTAP domains were elongated and triangular with feathery edges. Reducing the cooling rate or probe concentration for DPTAP bilayers resulted in larger, filled-in domains with more rounded edges. However, for DMTAP, cooling rates mainly affected size and only slightly modified domain morphology. In a saline environment, the domains were dark, and the surrounding continuous region was bright and thus contained the fluorescent probe. However, as the salt concentration was decreased, the dark regions percolated (connected), resulting in bright domains. Atomic force microscopy scans along domain edges revealed that the dark regions in fluorescence images were approximately 1.4 nm thicker than the light regions. Additionally, the dark regions were of bilayer thickness, approximately 4 nm. Comparison of these results in bilayers to well-documented behavior in Langmuir monolayers has revealed many similarities (and some differences) and is therefore useful for understanding our observations and identifying possible growth mechanisms that may occur in domain formation in cell membranes or supported membrane systems.
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