Three-dimensional structure of I(to): Kv4.2-KChIP2 ion channels by electron microscopy at 21 Angstrom resolution
Publication Type
Journal Article
Year of Publication
2004
Refereed Designation
Refereed
Journal
Neuron
Volume
41
Pagination
513-9
Date Published
Feb 19
ISSN
0896-6273 (Print)
Accession Number
14980201
Citation Key
66
Number
4
Keywords
"*Potassium Channels, Voltage-Gated", Animals, Calcium-Binding Proteins/chemistry/metabolism/*ultrastructure, Cell Membrane/metabolism/*ultrastructure, COS Cells, Humans, "Image Processing, Computer-Assisted", Kv Channel-Interacting Proteins, Membrane Pot
Abstract
Regulatory KChIP2 subunits assemble with pore-forming Kv4.2 subunits in 4:4 complexes to produce native voltage-gated potassium (Kv) channels like cardiac I(to) and neuronal I(A) subtypes. Here, negative stain electron microscopy (EM) and single particle averaging reveal KChIP2 to create a novel approximately 35 x 115 x 115 Angstrom, intracellular fenestrated rotunda: four peripheral columns that extend down from the membrane-embedded portion of the channel to enclose the Kv4.2 "hanging gondola" (a platform held beneath the transmembrane conduction pore by four internal columns). To reach the pore from the cytosol, ions traverse one of four external fenestrae to enter the rotundal vestibule and then cross one of four internal windows in the gondola.