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Photoswitchable fatty acids enable optical control of TRPV1

Author

Listed:
  • James Allen Frank

    (Ludwig Maximilians University Munich)

  • Mirko Moroni

    (Molecular Physiology of Somatic Sensation, Max Delbrück Center for Molecular Medicine)

  • Rabih Moshourab

    (Molecular Physiology of Somatic Sensation, Max Delbrück Center for Molecular Medicine
    Campus Charité Mitte und Virchow Klinikum, Charité Universitätsmedizin Berlin)

  • Martin Sumser

    (Ludwig Maximilians University Munich)

  • Gary R. Lewin

    (Molecular Physiology of Somatic Sensation, Max Delbrück Center for Molecular Medicine)

  • Dirk Trauner

    (Ludwig Maximilians University Munich)

Abstract

Fatty acids (FAs) are not only essential components of cellular energy storage and structure, but play crucial roles in signalling. Here we present a toolkit of photoswitchable FA analogues (FAAzos) that incorporate an azobenzene photoswitch along the FA chain. By modifying the FAAzos to resemble capsaicin, we prepare a series of photolipids targeting the Vanilloid Receptor 1 (TRPV1), a non-selective cation channel known for its role in nociception. Several azo-capsaicin derivatives (AzCAs) emerge as photoswitchable agonists of TRPV1 that are relatively inactive in the dark and become active on irradiation with ultraviolet-A light. This effect can be rapidly reversed by irradiation with blue light and permits the robust optical control of dorsal root ganglion neurons and C-fibre nociceptors with precision timing and kinetics not available with any other technique. More generally, we expect that photolipids will find many applications in controlling biological pathways that rely on protein–lipid interactions.

Suggested Citation

  • James Allen Frank & Mirko Moroni & Rabih Moshourab & Martin Sumser & Gary R. Lewin & Dirk Trauner, 2015. "Photoswitchable fatty acids enable optical control of TRPV1," Nature Communications, Nature, vol. 6(1), pages 1-11, November.
    • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8118
    DOI: 10.1038/ncomms8118
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