Mammalian axons express a rich repertoire of various K channel subtypes who
se distribution is profoundly affected by myelination. In the past two deca
des, functional analysis of axonal K channels has been approached primarily
through pharmacology. Recently, gene knockout techniques have been used to
specifically delete a particular K channel subtype from axons. This is sig
nificant since the bulk of K channels in a myelinated nerve are covered by
the myelin, making functional analysis of specific K channel subtypes by tr
aditional means difficult. This review summarizes the first mutational anal
ysis of this sort performed on an axonal fast K channel termed Kv1.1. This
K channel is concealed by the myelin loops in the paranodes of all major my
elinated fiber tracts, and exhibits highly heterogeneous distribution even
in certain non-myelinated CNS axons. Physiological analysis of Kv1.1 null m
utants suggest novel functions for this axonal K channel subtype, including
modulation of conduction failures at branch points and stabilization of tr
ansition zones in myelinated nerves.