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Gating charge displacement in voltage-gated ion channels involves limited transmembrane movement

Author

Listed:
  • Baron Chanda

    (David Geffen School of Medicine, UCLA)

  • Osei Kwame Asamoah

    (David Geffen School of Medicine, UCLA
    University of New Mexico Health Sciences Campus)

  • Rikard Blunck

    (David Geffen School of Medicine, UCLA)

  • Benoît Roux

    (Cornell University)

  • Francisco Bezanilla

    (David Geffen School of Medicine, UCLA
    Centro de Estudios Cientificos)

Abstract

Voltage-gated ion channels are responsible for generating electrical impulses in nerves and other excitable cells. The fourth transmembrane helix (S4) in voltage-gated channels is the primary voltage-sensing unit that mediates the response to a changing membrane electric field1,2. The molecular mechanism of voltage sensing, particularly with respect to the magnitude of the transmembrane movement of S4, remains controversial3,4,5. To determine the extent of this transmembrane movement, we use fluorescent resonance energy transfer between the S4 domain and a reference point in the lipid bilayer. The lipophilic ion dipicrylamine distributes on either side of the lipid bilayer depending on the membrane potential, and is used here as a resonance-energy-transfer acceptor from donor molecules attached to several positions in the Shaker K+ channel. A voltage-driven transmembrane movement of the donor should produce a transient fluorescence change because the acceptor also translocates as a function of voltage. In Shaker K+ channels no such transient fluorescence is observed, indicating that the S4 segment does not translocate across the lipid bilayer. Based on these observations, we propose a molecular model of voltage gating that can account for the observed 13e gating charge with limited transmembrane S4 movement.

Suggested Citation

  • Baron Chanda & Osei Kwame Asamoah & Rikard Blunck & Benoît Roux & Francisco Bezanilla, 2005. "Gating charge displacement in voltage-gated ion channels involves limited transmembrane movement," Nature, Nature, vol. 436(7052), pages 852-856, August.
  • Handle: RePEc:nat:nature:v:436:y:2005:i:7052:d:10.1038_nature03888
    DOI: 10.1038/nature03888
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    Cited by:

    1. Kazuki Obashi & Kem A. Sochacki & Marie-Paule Strub & Justin W. Taraska, 2023. "A conformational switch in clathrin light chain regulates lattice structure and endocytosis at the plasma membrane of mammalian cells," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

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