| Literature DB >> 16378393 |
Christophe Danelon1, Jean-Baptiste Perez, Christian Santschi, Jürgen Brugger, Horst Vogel.
Abstract
We present a method for spreading large (>100 microm(2)) cell membrane fragments across nanoapertures in planar supports. Electron-beam and focused-ion-beam lithography were used to fabricate arrays of 50-600 nm diameter holes in free-standing silicon nitride (SiN) solid films 100-500 nm thick. By pressing adhering live cells onto the nanostructured SiN surface and then removing them, planar cell membrane sheets (CMSs) were transferred in a well-defined orientation onto the SiN support. We demonstrate the accessibility to both extracellular and intracellular surfaces of CMSs by targeting membrane constituents side-specifically with fluorescent markers. Our approach is of interest for studying ligand-receptor interactions using optical, electrical, and scanning probe techniques at the single-molecule level.Entities:
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Year: 2006 PMID: 16378393 DOI: 10.1021/la052387v
Source DB: PubMed Journal: Langmuir ISSN: 0743-7463 Impact factor: 3.882