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      Engineering of supramolecular photoactive protein architectures: the defined co-assembly of photosystem I and cytochrome c using a nanoscaled DNA-matrix.

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          Abstract

          The engineering of renewable and sustainable protein-based light-to-energy converting systems is an emerging field of research. Here, we report on the development of supramolecular light-harvesting electrodes, consisting of the redox protein cytochrome c working as a molecular scaffold as well as a conductive wiring network and photosystem I as a photo-functional matrix element. Both proteins form complexes in solution, which in turn can be adsorbed on thiol-modified gold electrodes through a self-assembly mechanism. To overcome the limited stability of self-grown assemblies, DNA, a natural polyelectrolyte, is used as a further building block for the construction of a photo-active 3D architecture. DNA acts as a structural matrix element holding larger protein amounts and thus remarkably improving the maximum photocurrent and electrode stability. On investigating the photophysical properties, this system demonstrates that effective electron pathways have been created.

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          Author and article information

          Journal
          Nanoscale
          Nanoscale
          Royal Society of Chemistry (RSC)
          2040-3372
          2040-3364
          May 19 2016
          : 8
          : 20
          Affiliations
          [1 ] Technical University of Applied Sciences Wildau, Institute of Applied Life Sciences, Biosystems Technology, Hochschulring 1, 15745 Wildau, Germany. flisdat@th-wildau.de.
          [2 ] Humboldt-University of Berlin, Institute of Biology, Biochemistry and Structural Biology, Unter den Linden 6, 10099 Berlin, Germany.
          [3 ] University of Glasgow, Glasgow Biomedical Research Centre, Institute for Molecular, Cell & Systems Biology, 120 University Place, Glasgow, G12 8TA, Scotland, UK.
          Article
          10.1039/c6nr00097e
          27150202
          37757ce3-aff1-4111-84c8-1b83257b0ef9
          History

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