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.