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Biophys J, February 1998, p. 722-730, Vol. 74, No. 2
*Department of Animal Physiology, Institute of Zoology, University of Salzburg, A-5020 Salzburg, Austria, and #Institute of Pharmaceutical Chemistry, University of Innsbruck, A-6020 Innsbruck, Austria
In this study we compared polyamines to various diamines,
and we modeled flexibility as well as hydrophobicity properties of
these molecules to examine possible structural differences that could
explain their external effects on the channels. The natural polyamines
(putrescine, cadaverine, spermidine, spermine) and diamines increasing
in CH2 chain length from C2 to C12 were used to probe maxi
calcium-activated potassium (BK) channels in GH3 pituitary tumor cells
when applied extracellularly. In single-channel recordings we found
polyamines as well as diamines up to 1,10-diaminodecane to be
ineffective in altering channel current amplitudes or kinetics. In
contrast, 1,12-diamino dodecane (1,12-DD) was found to be a reversible
blocker, with a blocking site at an electrical distance (z
) of 0.72 within the channel. It reduced
single-channel current amplitude, mean channel open time, and channel
open probability. In computer simulations structural data, such as
flexibility, hydration, and log D values, were
calculated. 1,12-DD showed the largest flexibility of all diamines
(minimum N-N distance 9.9 Å) combined with a marked hydrophobicity due
to a 4-5 Å hydrophobic intersegment between hydrophilic ends in the
molecule, as confirmed by GRID water probe maps and a log
D value of
1.82 at pH 7.2. We propose that the amount
of hydration of the molecule, more than its flexibility, constitutes an
essential parameter for its ability to act as a channel blocker.
Biophys J, February 1998, p. 722-730, Vol. 74, No. 2
© 1998 by the Biophysical Society 0006-3495/98/02/722/09 $2.00
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