Functional expression of Drosophila para sodium channels. Modulation by the membrane protein TipE and toxin pharmacology.

ABSTRACT: The Drosophila para sodium channel alpha subunit was expressed in Xenopus oocytes alone and in combination with tipE, a putative Drosophila sodium channel accessory subunit. Coexpression of tipE with para results in elevated levels of sodium currents and accelerated current decay. Para/TipE sodium channels have biophysical and pharmacological properties similar to those of native channels. However, the pharmacology of these channels differs from that of vertebrate sodium channels: (a) toxin II from Anemonia sulcata, which slows inactivation, binds to Para and some mammalian sodium channels with similar affinity (Kd congruent with 10 nM), but this toxin causes a 100-fold greater decrease in the rate of inactivation of Para/TipE than of mammalian channels; (b) Para sodium channels are >10-fo

SUBMITTER: Warmke JW 

PROVIDER: S-EPMC2233785 | biostudies-literature | 1997 Aug

REPOSITORIES: biostudies-literature