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Biophys J, November 2000, p. 2475-2493, Vol. 79, No. 5
Scuola Internazionale Superiore di Studi Avanzati & Instituto Nationale di Fiscia del la Materia-Unita' di Trieste, 34014 Trieste, Italy
The permeability ratio between K+ and
Na+ ions in cyclic nucleotide-gated channels is close to 1, and the single channel conductance has almost the same value in the
presence of K+ or Na+. Therefore,
K+ and Na+ ions are thought to permeate with
identical properties. In the
-subunit from bovine rods there is a
loop of three prolines at positions 365 to 367. When proline 365 is
mutated to a threonine, a cysteine, or an alanine, mutant channels
exhibit a complex interaction between K+ and
Na+ ions. Indeed K+, Rb+ and
Cs+ ions do not carry any significant macroscopic current
through mutant channels P365T, P365C and P365A and block the current
carried by Na+ ions. Moreover in mutant P365T the presence
of K+ in the intracellular (or extracellular) medium caused
the appearance of a large transient inward (or outward) current carried
by Na+ when the voltage command was quickly stepped to
large negative (or positive) membrane voltages. This transient current
is caused by a transient potentiation, i.e., an increase of the open
probability. The permeation of organic cations through these mutant
channels is almost identical to that through the wild type
(w.t.) channel. Also in the w.t. channel a similar but smaller
transient current is observed, associated to a slowing down of the
channel gating evident when intracellular Na+ is replaced
with K+. As a consequence, a rather simple mechanism can
explain the complex behavior here described: when a K+ ion
is occupying the pore there is a profound blockage of the channel and a
potentiation of gating immediately after the K+ ion is
driven out. Potentiation occurs because K+ ions slow down
the rate constant Koff controlling channel closure. These
results indicate that K+ and Na+ ions do not
permeate through CNG channels in the same way and that K+
ions influence the channel gating.
Biophys J, November 2000, p. 2475-2493, Vol. 79, No. 5
© 2000 by the Biophysical Society 0006-3495/00/11/2475/19 $2.00
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