Electrophysiological studies of neurons reveal different Ca2+ currents desi
gnated L-, N-, P-, Q-, R-, and T-type. High-voltage-activated neuronal Ca2 channels are complexes of a pore-forming al subunit of about 190-250 kDa,
a transmembrane, disulfide-linked complex of alpha 2 and delta subunits, an
d an intracellular beta subunit, similar to the alpha 1, alpha 2 delta, and
beta subunits previously described for skeletal muscle Ca2+ channels. The
primary structures of these subunits have all been determined by homology c
DNA cloning using the corresponding subunits of skeletal muscle Ca2+ channe
ls as probes. In most neurons, L-type channels contain alpha(1C) or alpha(1
D) subunits, N-type contain alpha(1B) subunits, P- and Q-types contain alte
rnatively spliced forms of alpha(1A) subunits, R-type contain alpha(1E) sub
units, and T-type contain alpha(1G) or alpha(1H) subunits. Association with
different beta subunits also influences Ca2+ channel gating substantially,
yielding a remarkable diversity of functionally distinct molecular species
of Ca2+ channels in neurons.