0000000000685398

AUTHOR

Stephanie Künneke

showing 4 related works from this author

Scrutiny of the Failure of Lipid Membranes As A Function of Headgroups, Chain Length, and Lamellarity Measured by Scanning Force Microscopy

2004

AbstractA fast, quantitative, and unambiguous screening of material properties of biomembranes using scanning force microscopy in pulsed force mode on lipid membranes is presented. The spatially resolved study of breakthrough force, breakthrough distance, adhesion, stiffness, and topography of lipid membranes as determined simultaneously by digitalized pulsed force mode provides new insight into the structure-function relationship of model membranes, which are systematically analyzed by varying chain length, lipid headgroup, and lamellarity. For this purpose, a novel unbiased analysis method is presented. A strong correlation between adhesion and breakthrough events is found on lipid bilaye…

Macromolecular SubstancesMembrane FluidityLipid BilayersBiophysicsAnalytical chemistryMolecular ConformationMicroscopy Atomic ForceMicromanipulationMotionStructure-Activity RelationshipMicroscopyMaterials TestingmedicineMembrane fluidityLipid bilayerLiposomeMembranesChemistrytechnology industry and agricultureStiffnessMembranes ArtificialElasticityMembraneStructural stabilityLiposomesBiophysicslipids (amino acids peptides and proteins)Stress Mechanicalmedicine.symptomMaterial properties
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Rasterkraftmikroskopische In-situ-Detektion von molekularen Erkennungsreaktionen an mikrostrukturierten Lipidmembransegmenten

2002

ChemistryGeneral MedicineAngewandte Chemie
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Visualization of Molecular Recognition Events on Microstructured Lipid-Membrane Compartments by In Situ Scanning Force Microscopy This work was suppo…

2002

In situScanning probe microscopyMolecular recognitionChemistryScanning confocal electron microscopyScanning ion-conductance microscopyNanotechnologyGeneral ChemistryLipid bilayerBiosensorCatalysisSoft lithographyAngewandte Chemie International Edition
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Lateral organization of G M1 in phase-separated monolayers visualized by scanning force microscopy

2002

Phase separation of glycolipids in lipid mono- and bilayers is of great interest for the understanding of membrane function. The distribution of the ganglioside GM1 in sphingomyelin (SM)/1-palmitoyl-2-oleoyl- sn-glycero-3-phosphocholine (POPC), SM/1,2-dipalmitoyl- sn-glycero-3-phosphocholine (DOPC) and SM/cholesterol/POPC Langmuir-Blodgett (LB) monolayers transferred at 36 mN/m has been studied by scanning force microscopy. Besides lateral organization of the glycolipid in LB monolayers as deduced from topography, material properties have been investigated by phase imaging, pulsed force mode and force modulation microscopy. It was shown that GM1 preferentially clusters in an ordered lipid m…

Aqueous solutionChemistryLipid BilayersBiophysicsAnalytical chemistryBrainMembranes ArtificialG(M1) GangliosideGeneral MedicineMicroscopy Atomic ForceLipidsMicelleSphingomyelinschemistry.chemical_compoundCrystallographyCholesterolGlycolipidPhase (matter)MicroscopyMonolayerPhosphatidylcholinesSphingomyelinPOPCEuropean Biophysics Journal
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