Ion channel targeting within neuronal and muscle membranes is an important
determinant of electrical excitability, Recent evidence suggests that there
exists within the membrane specialized microdomains commonly referred to a
s lipid rafts. These domains are enriched in cholesterol and sphingolipids
and concentrate a number of signal transduction proteins such as nitric-oxi
de synthase, ligand-gated receptors, and multiple protein kinases, Here, we
demonstrate that the voltage-gated K+ channel Kv2.1, but not Kv4.2, target
s to lipid rafts in both heterologous expression sg systems and rat brain.
The Kv2.1 association with lipid rafts does not appear to involve caveolin.
Depletion of cellular cholesterol alters the buoyancy of the Kv2.1 associa
ted rafts and shifts the midpoint of Kv2.1 inactivation by nearly 40 mV wit
hout affecting peak current density or channel activation. The differential
targeting of K+ channels to lipid rafts represents a novel mechanism both
for the subcellular sorting of K+ channels to regions of the membrane rich
in signaling complexes and for modulating channel properties via alteration
s in lipid content.