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Engineering Cell-permeable Protein
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Bioengineering a Single-Protein Junction.

Marta P Ruiz1,2,3, Albert C Aragonès1,2,3, Nuria Camarero2,3

  • 1Departament of Materials Science and Physical Chemistry & Institute of Theoretical and Computational Chemistry (IQTCUB), University of Barcelona , Martí i Franquès, 1, Barcelona 08028, Spain.

Journal of the American Chemical Society
|October 6, 2017
PubMed
Summary
This summary is machine-generated.

Researchers engineered charge transport in single proteins by altering a single mutation. This mutation shifted electron transfer from a two-step process to direct tunneling, demonstrating control over bioelectronic properties.

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Area of Science:

  • Bioelectronics
  • Nanotechnology
  • Protein Engineering

Background:

  • Designing nanoscale electronic platforms for in vivo determinations requires interfacing biomolecular sensing units with electronic platforms for signal transduction.
  • Understanding the electrical signatures of biomolecular circuits is crucial for tailoring their electrical properties.

Purpose of the Study:

  • To demonstrate bioengineered charge transport in a single-protein electrical contact.
  • To investigate the effect of a single point-site mutation on protein charge transport behavior.

Main Methods:

  • Fabrication of single-protein electrical contacts using Cu-azurin.
  • Introduction of a single point-site mutation at the docking hydrophobic patch.
  • Spectroscopic studies and molecular-dynamics simulations.
  • Density Functional Theory (DFT) computations of frontier orbitals.

Main Results:

  • A single mutation dramatically altered the charge transport regime from Cu-mediated two-step transport to direct coherent tunneling.
  • Minor structural distortion of the protein blue Cu site was observed.
  • Protein folding structures were preserved in the single-protein junction.
  • DFT analysis suggested Cu center participation in the observed charge transport differences.

Conclusions:

  • Demonstrated direct control over charge transport in a protein backbone via external mutagenesis.
  • Established a nanoscale platform for studying structure-related biological electron transfer.
  • Highlighted the potential of bioengineering for tailoring protein electrical properties in bioelectronic devices.