Abstract

The functional fusion of “living” biomaterial (such as cells) with synthetic systems has developed into a principal ambition for various scientific disciplines. In particular, emerging fields such as bionics and nanomedicine integrate advanced nanomaterials with biomolecules, cells and organisms in order to develop novel strategies for applications, including energy production or real-time diagnostics utilizing biomolecular machineries “perfected” during billion years of evolution. To date, hardware–wetware interfaces that sample or modulate bioelectric potentials, such as neuroprostheses or implantable energy harvesters, are mostly based on microelectrodes brought into the closest possible contact with the targeted cells. Recently, the possibility of using electrochemical gradients of the inner ear for technical applications was demonstrated using implanted electrodes, where 1.12 nW of electrical power was harvested from the guinea pig endocochlear potential for up to 5 h (Mercier, P.; Lysaght, A.; Bandyopadhyay, S.; Chandrakasan, A.; Stankovic, K. Nat. Biotech. 2012, 30, 1240–1243). More recent approaches employ nanowires (NWs) able to penetrate the cellular membrane and to record extra- and intracellular electrical signals, in some cases with subcellular resolution (Spira, M.; Hai, A. Nat. Nano. 2013, 8, 83–94). Such techniques include nanoelectric scaffolds containing free-standing silicon NWs (Robinson, J. T.; Jorgolli, M.; Shalek, A. K.; Yoon, M. H.; Gertner, R. S.; Park, H. Nat Nanotechnol. 2012, 10, 180–184) or NW field-effect transistors (Qing, Q.; Jiang, Z.; Xu, L.; Gao, R.; Mai, L.; Lieber, C. Nat. Nano. 2013, 9, 142–147), vertically aligned gallium phosphide NWs (Hällström, W.; Mårtensson, T.; Prinz, C.; Gustavsson, P.; Montelius, L.; Samuelson, L.; Kanje, M. Nano Lett. 2007, 7, 2960–2965) or individually contacted, electrically active carbon nanofibers. The latter of these approaches is capable of recording electrical responses from oxidative events occurring in intercellular regions of neuronal cultures (Zhang, D.; Rand, E.; Marsh, M.; Andrews, R.; Lee, K.; Meyyappan, M.; Koehne, J. Mol. Neurobiol. 2013, 48, 380–385). Employing monocrystalline gold, nanoelectrode interfaces, we have now achieved stable, functional access to the electrochemical machinery of individual Physarum polycephalum slime mold cells. We demonstrate the “symbionic” union, allowing for electrophysiological measurements, functioning as autonomous sensors and capable of producing nanowatts of electric power. This represents a further step towards the future development of groundbreaking, cell-based technologies, such as bionic sensory systems or miniaturized energy sources to power various devices, or even “intelligent implants”, constantly refueled by their surrounding nutrients.

Highlights

  • We demonstrate the “symbionic” union, allowing for electrophysiological measurements, functioning as autonomous sensors and capable of producing nanowatts of electric power

  • Monocrystalline gold (Au) nanowires in parallel arrangement featuring homogenous, low defect and parallel-oriented crystal planes were produced by electrodeposition as previously described [1]

  • This view is corroborated by our own (Supporting Information File 1, Figure S1a) as well as other various electrophysiology studies, observing rapid ejection of intracellular glass microelectrodes from Physarum p. [10]. This is presumably due to its pronounced membrane regenerative ability. In line with this notion, the observed voltage drop was accelerated when nanoelectrode interfaces (NEIs) measurements were performed without additional pressure applied to the electrode (Supporting Information File 1, Figure S1c)

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Summary

Functional fusion of living systems with synthetic electrode interfaces

Address: 1Max-Planck Institute for Intelligent Systems, Department of New Materials and Biosystems, Heisenbergstraße 3, D-70569 Stuttgart, Germany, 2German Cancer Research Center, DKFZ Life Science Lab, Im Neuenheimer Feld 581, D-69120 Heidelberg, Germany, 3Bachelor Program Molecular Biotechnology, University of Heidelberg, Institute of Pharmacy and Molecular Biotechnology, Im Neuenheimer Feld 364, D-69120 Heidelberg, Germany, 4Department of Neurobiology, Interdisciplinary Centre for Neurosciences (IZN), University of Heidelberg, Im Neuenheimer Feld 364, D-69120 Heidelberg, Germany, and 5University of Heidelberg, Department of Biophysical Chemistry, Im Neuenheimer Feld 253, D-69120 Heidelberg, Germany

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