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JBC, Vol. 254, Issue 22, 11199-11201, Nov, 1979
V. A. Rhoden and S. M. Goldin
Saturable, high affinity binding of tritium-labeled saxitoxin ([3H]STX) to
axolemma-enriched membranes from white matter of bovine brain was
identified. The apparent [3H]STX equilibrium dissociation constant (Kd*)
was strongly affected by the cationic environment:choline ion had little
effect; cesium ion increased the mammalian axolemma Kd* in a simple
competitive manner. In contrast, sodium ion more dramatically increased the
Kd*--this effect was highly cooperative between 75 and 200 mM sodium (Hill
coefficient of 2.85). The cooperativity is most pronounced at the normally
expected [sodium] external to the axon in the mammalian central nervous
system. This sodium-specific cooperative modification of the STX binding
site (the hypothetical "ion selectivity filter" of the axonal Na+ gate) may
be indicative of some as yet undefined regulatory mechanism of the Na+ gate
in mammalian myelinated axons.
The binding of saxitoxin to axolemma of mammalian brain. Cooperative competition between saxitoxin and sodium ion
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