TY - JOUR
T1 - Gating charge displacement in voltage-gated ion channels involves limited transmembrane movement
AU - Chanda, Baron
AU - Asamoah, Osei Kwame
AU - Blunck, Rikard
AU - Roux, Benoît
AU - Bezanilla, Francisco
N1 - Funding Information:
Acknowledgements We thank M. J. Hahn for technical assistance, M. Holmgren for the cysteine-less Shaker clone, W. Hubell for the gift of dipicrylamine and the members of Bezanilla and Correa laboratories for their comments. This work was supported by funds from an AHA postdoctoral fellowship to B.C., NRSA funding to O.K.A, DFG funding to R.B. and an NIH grant to F.B.
PY - 2005/8/11
Y1 - 2005/8/11
N2 - 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 field. The molecular mechanism of voltage sensing, particularly with respect to the magnitude of the transmembrane movement of S4, remains controversial. 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.
AB - 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 field. The molecular mechanism of voltage sensing, particularly with respect to the magnitude of the transmembrane movement of S4, remains controversial. 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.
UR - https://www.scopus.com/pages/publications/23844459909
U2 - 10.1038/nature03888
DO - 10.1038/nature03888
M3 - Article
C2 - 16094369
AN - SCOPUS:23844459909
SN - 0028-0836
VL - 436
SP - 852
EP - 856
JO - Nature
JF - Nature
IS - 7052
ER -