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Tracking a complete voltage-sensor cycle with metal-ion bridges.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2012 May 29; Vol. 109 (22), pp. 8552-7. Date of Electronic Publication: 2012 Apr 25. - Publication Year :
- 2012
-
Abstract
- Voltage-gated ion channels open and close in response to changes in membrane potential, thereby enabling electrical signaling in excitable cells. The voltage sensitivity is conferred through four voltage-sensor domains (VSDs) where positively charged residues in the fourth transmembrane segment (S4) sense the potential. While an open state is known from the Kv1.2/2.1 X-ray structure, the conformational changes underlying voltage sensing have not been resolved. We present 20 additional interactions in one open and four different closed conformations based on metal-ion bridges between all four segments of the VSD in the voltage-gated Shaker K channel. A subset of the experimental constraints was used to generate Rosetta models of the conformations that were subjected to molecular simulation and tested against the remaining constraints. This achieves a detailed model of intermediate conformations during VSD gating. The results provide molecular insight into the transition, suggesting that S4 slides at least 12 Å along its axis to open the channel with a 3(10) helix region present that moves in sequence in S4 in order to occupy the same position in space opposite F290 from open through the three first closed states.
- Subjects :
- Animals
Binding Sites genetics
Cadmium chemistry
Cadmium metabolism
Chelating Agents pharmacology
Computer Simulation
Drosophila Proteins chemistry
Drosophila Proteins genetics
Drosophila melanogaster genetics
Drosophila melanogaster metabolism
Egtazic Acid pharmacology
Female
Ion Channel Gating genetics
Kinetics
Membrane Potentials drug effects
Membrane Potentials physiology
Metals chemistry
Models, Molecular
Mutation
Oocytes drug effects
Oocytes metabolism
Oocytes physiology
Patch-Clamp Techniques
Protein Binding
Protein Structure, Tertiary
Shaker Superfamily of Potassium Channels chemistry
Shaker Superfamily of Potassium Channels genetics
Xenopus laevis
Drosophila Proteins metabolism
Ion Channel Gating physiology
Metals metabolism
Shaker Superfamily of Potassium Channels metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 109
- Issue :
- 22
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 22538811
- Full Text :
- https://doi.org/10.1073/pnas.1116938109