Author
Listed:
- Michael Hirtz
(Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT))
- Antonios Oikonomou
(School of Computer Science and Centre for Mesoscience and Nanotechnology, The University of Manchester)
- Thanasis Georgiou
(School of Physics and Astronomy, The University of Manchester)
- Harald Fuchs
(Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT)
Physical Institute and Center for Nanotechnology (CeNTech), University of Münster)
- Aravind Vijayaraghavan
(School of Materials and Centre for Mesoscience and Nanotechnology, The University of Manchester)
Abstract
The application of graphene in sensor devices depends on the ability to appropriately functionalize the pristine graphene. Here we show the direct writing of tailored phospholipid membranes on graphene using dip-pen nanolithography. Phospholipids exhibit higher mobility on graphene compared with the commonly used silicon dioxide substrate, leading to well-spread uniform membranes. Dip-pen nanolithography allows for multiplexed assembly of phospholipid membranes of different functionalities in close proximity to each other. The membranes are stable in aqueous environments and we observe electronic doping of graphene by charged phospholipids. On the basis of these results, we propose phospholipid membranes as a route for non-covalent immobilization of various functional groups on graphene for applications in biosensing and biocatalysis. As a proof of principle, we demonstrate the specific binding of streptavidin to biotin-functionalized membranes. The combination of atomic force microscopy and binding experiments yields a consistent model for the layer organization within phospholipid stacks on graphene.
Suggested Citation
Michael Hirtz & Antonios Oikonomou & Thanasis Georgiou & Harald Fuchs & Aravind Vijayaraghavan, 2013.
"Multiplexed biomimetic lipid membranes on graphene by dip-pen nanolithography,"
Nature Communications, Nature, vol. 4(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3591
DOI: 10.1038/ncomms3591
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