Quantitative investigation by atomic force microscopy of supported phospholipid layers and nanostructures on cholesterol-functionalized glass surfaces

Understanding the interaction mechanisms of phospholipids with surfaces is crucial for the exploitation of lipid bilayers as models of the cell membrane as well as templates for biosensors. Moreover, controlling and manipulating lipid nanoparticles for the investigation of their properties by means...

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Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 24(2008), 15 vom: 05. Aug., Seite 7830-41
1. Verfasser: Indrieri, Marco (VerfasserIn)
Weitere Verfasser: Suardi, Marco, Podestà, Alessandro, Ranucci, Elisabetta, Ferruti, Paolo, Milani, Paolo
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Ethylenediamines Phospholipids Polyethylene Glycols 3WJQ0SDW1A ethylenediamine 60V9STC53F Cholesterol 97C5T2UQ7J
Beschreibung
Zusammenfassung:Understanding the interaction mechanisms of phospholipids with surfaces is crucial for the exploitation of lipid bilayers as models of the cell membrane as well as templates for biosensors. Moreover, controlling and manipulating lipid nanoparticles for the investigation of their properties by means of single-particle sensitive surface techniques require the ability to tailor the chemical properties of surfaces to achieve a stable and sparse binding of lipid particles, while keeping them from aggregating, or denaturing. Here we present a quantitative morphological and structural investigation by atomic force microscopy of supported phospholipid layers and nanostructures on cholesterol-functionalized glass surfaces, in comparison with other surfaces with different interfacial properties. We show that the functionalization of glass coverslips with cholesterol groups is a viable route for the production of optically transparent, scanning probe microscopy-compatible clean substrates for the effective immobilization of both extended single lipid bilayers and lipid nanoparticles
Beschreibung:Date Completed 08.09.2008
Date Revised 01.12.2018
published: Print-Electronic
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/la703725b