Cell Membranes Suspended Across Nanoaperture Arrays

Christophe Danelon, Jean-Baptiste Perez, Christian Santschi,§ Jürgen Brugger,§ and Horst Vogel*
Laboratory of Physical Chemistry of Polymers and Membranes, and Microsystems Laboratory, Ecole Polytechnique Fdrale de Lausanne (EPFL), 1015 Lausanne, Switzerland
Langmuir, 2006, 22 (1), pp 22–25
DOI: 10.1021/la052387v
Publication Date (Web): December 1, 2005
Copyright © 2006 American Chemical Society

 Laboratory of Physical Chemistry of Polymers and Membranes.

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 Microsystems Laboratory.

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 To whom correspondence should be addressed. E-mail:  horst.vogel@epfl.ch.

Abstract

Abstract Image

We present a method for spreading large (>100 μm2) 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.

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History

  • Published In Issue January 03, 2006
  • Received September 1, 2005
    Revised October 28, 2005

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