S4-based voltage sensors have three major conformations
ORCiD
0000-0002-6489-4651
Document Type
Article
Publication Title
Proceedings of the National Academy of Sciences of the United States of America
ISSN
1091-6490
Volume
105
Issue
46
DOI
10.1073/pnas.0807387105
First Page
17600
Last Page
17607
Publication Date
11-18-2008
Abstract
Voltage sensors containing the charged S4 membrane segment display a gating charge vs. voltage (Q-V) curve that depends on the initial voltage. The voltage-dependent phosphatase (Ci-VSP), which does not have a conducting pore, shows the same phenomenon and the Q-V recorded with a depolarized initial voltage is more stable by at least 3RT. The leftward shift of the Q-V curve under prolonged depolarization was studied in the Ci-VSP by using electrophysiological and site-directed fluorescence measurements. The fluorescence shows two components: one that traces the time course of the charge movement between the resting and active states and a slower component that traces the transition between the active state and a more stable state we call the relaxed state. Temperature dependence shows a large negative enthalpic change when going from the active to the relaxed state that is almost compensated by a large negative entropic change. The Q-V curve midpoint measured for pulses that move the sensor between the resting and active states, but not long enough to evolve into the relaxed states, show a periodicity of 120 degrees, indicating a 3(10) secondary structure of the S4 segment when determined under histidine scanning. We hypothesize that the S4 segment moves as a 3(10) helix between the resting and active states and that it converts to an alpha-helix when evolving into the relaxed state, which is most likely to be the state captured in the crystal structures.
Recommended Citation
Villalba-Galea, C. A.,
Sandtner, W.,
Starace, D. M.,
&
Bezanilla, F.
(2008).
S4-based voltage sensors have three major conformations.
Proceedings of the National Academy of Sciences of the United States of America, 105(46), 17600–17607.
DOI: 10.1073/pnas.0807387105
https://scholarlycommons.pacific.edu/phs-facarticles/307