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Binding of an α scorpion toxin to insect sodium channels is not dependent on membrane potential
Author(s) -
Gordon Dalia,
Zlotkin Eliahu
Publication year - 1993
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(93)81147-r
Subject(s) - scorpion , sodium channel , scorpion toxin , insect , toxin , membrane potential , chemistry , sodium , scorpion venoms , biophysics , biology , venom , biochemistry , botany , organic chemistry
The insect‐specific LqhαIT toxin resembles α scorpion toxins affecting mammals by its amino acid sequence and effects on sodium conductance. The present study reveals that LqhαIT does not bind to rat brain membranes and possesses in locust neuronal membranes a single class of high affinity ( K d = 1.06 ± 0.15 nM) and low capacity ( B max = 0.7 ± 0.19 protein) binding sites. The latter are: (1) distinct from binding sites of other sodium channel neurotoxins; (2) inhibited by sea anemone toxin II; (3) cooperatively interacting with veratridine; (4) not dependent on membrane potential, in contrast to the binding sites of α toxins in vertebrate systems. These data suggest the occurrence of (a) conformational‐structural differences between insect and mammal sodium channels and (b) the animal group specificity and pharmacological importance of the α scorpion toxins.