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Remote control of ion channels and neurons through magnetic-field heating of nanoparticles

Nature Nanotechnology volume 5, pages 602606 (2010) | Download Citation

Abstract

Recently, optical stimulation1,2,3 has begun to unravel the neuronal processing that controls certain animal behaviours4,5. However, optical approaches are limited by the inability of visible light to penetrate deep into tissues. Here, we show an approach based on radio-frequency magnetic-field heating of nanoparticles to remotely activate temperature-sensitive cation channels in cells. Superparamagnetic ferrite nanoparticles were targeted to specific proteins on the plasma membrane of cells expressing TRPV1, and heated by a radio-frequency magnetic field. Using fluorophores as molecular thermometers, we show that the induced temperature increase is highly localized. Thermal activation of the channels triggers action potentials in cultured neurons without observable toxic effects. This approach can be adapted to stimulate other cell types and, moreover, may be used to remotely manipulate other cellular machinery for novel therapeutics.

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Acknowledgements

The authors thank F. Qin for the TRPV1 plasmid and initial assistance, A. Ting for the biotin acceptor peptide-cyan fluorescent protein-transmembrane (AP-CFP-TM) and BirA constructs, and O. Griesbeck for the TN-XL plasmid. J. Pazik is acknowledged for technical assistance, and Y. Hsu, V. Rana, M.J. Ezak and M. Zugravu for valuable discussions.

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Affiliations

  1. Department of Physics, University at Buffalo, the State University of New York, Buffalo, New York 14260, USA

    • Heng Huang
    • , Savas Delikanli
    • , Hao Zeng
    •  & Arnd Pralle
  2. Department of Biological Sciences, University at Buffalo, the State University of New York, Buffalo, New York 14260, USA

    • Denise M. Ferkey

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Contributions

A.P. designed the study. H.H. carried out nanoparticle coating and cellular measurements. S.D. and H.Z. were responsible for nanoparticle synthesis and characterization, and D.M.F. for the C. elegans experiments. A.P. and H.H. wrote the manuscript. All authors discussed the results and commented on the manuscript. The work was supported by NSF DMR-0547036, UB IRDF, RF and INSIF.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Arnd Pralle.

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DOI

https://doi.org/10.1038/nnano.2010.125

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