FuSyMEM: Functional Synthetic Membranes for GPCR based Sensing

Duration: 36 months

Coordinator: MPI for Polymer Research (Germany)

Websitefusymem.epfl.ch

Contact Person:

Dr. Eva-Kathrin Sinner
MPI for Polymer Research
Ackermannweg 10
55128 Mainz, Germany
e-mail: sinner[at]mpip-mainz.mpg.de
tel: +49 6131 37 91 61
fax: +49 6131 37 93 26


Partners
:

  • Chalmers University of Technology (Sweden)
  • Ecole Polytechnique Fédérale de Lausanne (Switzerland)
  • Universität Basel (Switzerland)

 

Project Description:

Odorant receptors, members of the GPCR family, are an excellent example of natural superiority in binding specificity of small and hydrophobic molecules. But difficulties in expression, isolation and solubilisation of GPCRs hampered the assay development and further applications in sensor devices far. We propose modular engineering, including an in vitro strategy for protein expression in combination with synthetic amphiphiles mimicking a cell membrane, thus preserving the structural functional integrity of the GPCRs. By addition of the mere genetic information of the protein of interest, de novo protein synthesis and insertion in a supported membrane has been observed, recently. With the challenging example of odorant receptors as GPCR species, we would like to expand these findings towards a robust sensor platform taking advantage of the odorant receptors’ superior recognition potential of small hydrophobic molecules. Synthetic materials, with suitable amphiphilic properties as structural analogues to phospholipids, provide untapped design potential mimicking native membrane architectures. Use of these synthetic amphiphiles broadens the spectrum of sensor application towards air-borne sensors. The assembly of a synthetic membrane layer on the sensor surface by fusion of block copolymer vesicles and the functional incorporation of GPCReceptors will be monitored by a quartz crystal microbalance (QCM-D), sensitive to detect the membrane formation as well as the protein insertion even in the presence of optically opaque cell extracts. Surface enhanced fluorescence spectroscopy will be employed to verify the oriented, functional incorporation of the odorant receptors into the polymer membrane matrix. Structural and mobility properties of the membrane embedded proteins will be analyzed at the single-molecule level based on image correlation microscopy. Ultimately, ligand-receptor interactions will be assessed on a new sensor concept via optical and mechanical means.

(source: Cordis Nest Pathfinder projects 2003-2006)