Open AccessCompletely functional double-barreled chloride channel expressed from a single Torpedo cDNA.
Author(s) -
Christiane K. Bauer,
Klaus Steinmeyer,
J. R. Schwarz,
Thomas J. Jentsch
Publication year - 1991
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.88.24.11052
Subject(s) - torpedo , xenopus , complementary dna , chloride channel , biophysics , electrophysiology , biology , microbiology and biotechnology , chemistry , biochemistry , gene , acetylcholine receptor , neuroscience , receptor
We have performed an electrophysiological analysis of the recently cloned Torpedo marmorata Cl- channel. Functional expression of Cl- channels in oocytes of Xenopus laevis previously injected with cRNA yielded an outward-rectifying current activated by hyperpolarization. Replacement of Cl- with other anions significantly reduced or inhibited the current. Single-channel recordings from cell-attached patches exhibited burst-like Cl- channel activity with rapid fluctuations between three equally spaced substates (0 pS, 9 pS, and 18 pS). The properties of the cloned Cl- channel were almost identical to those of the reconstituted native T. californica Cl- channel and were in full agreement with the predictions of the double-barreled channel model [Hanke, W. & Miller, C. (1983) J. Gen. Physiol. 82, 25-45]. Our results imply that the cloned cDNA codes for the completely functional Torpedo electroplax Cl- channel.
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