Gating of the voltage-dependent chloride channel CIC-0 by the permeant anion
- 1 February 1995
- journal article
- Published by Springer Nature in Nature
- Vol. 373 (6514) , 527-531
- https://doi.org/10.1038/373527a0
Abstract
Chloride channels of the ClC family are important for the control of membrane excitability, cell volume regulation, and possibly transepithelial transport. Although lacking the typical voltage-sensor found in cation channels, gating of ClC channels is clearly voltage-dependent. For the prototype Torpedo channel ClC-0 (refs 11-15) we now show that channel opening is strongly facilitated by external chloride. Other less permeable anions can substitute for chloride with less efficiency. ClC-0 conductance shows an anomalous mole fraction behaviour with Cl-/NO3- mixtures, suggesting a multi-ion pore. Gating shows a similar anomalous behaviour, tightly linking permeation to gating. Eliminating a positive charge at the cytoplasmic end of domain D12 changes kinetics, concentration dependence and halide selectivity of gating, and alters pore properties such as ion selectivity, single-channel conductance and rectification. Taken together, our results strongly suggest that in these channels voltage-dependent gating is conferred by the permeating ion itself, acting as the gating charge.Keywords
This publication has 29 references indexed in Scilit:
- Two highly homologous members of the ClC chloride channel family in both rat and human kidney.Proceedings of the National Academy of Sciences, 1994
- Voltage gating of ion channelsQuarterly Reviews of Biophysics, 1994
- Regions involved in the opening of CIC-2 chloride channel by voltage and cell volumeNature, 1992
- The Skeletal Muscle Chloride Channel in Dominant and Recessive Human MyotoniaScience, 1992
- A chloride channel widely expressed in epithelial and non-epithelial cellsNature, 1992
- Inactivation of muscle chloride channel by transposon insertion in myotonic miceNature, 1991
- Alteration of voltage-dependence of Shaker potassium channel by mutations in the S4 sequenceNature, 1991
- Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytesNature, 1990
- Structural parts involved in activation and inactivation of the sodium channelNature, 1989
- Single chloride channels from Torpedo electroplax. Activation by protons.The Journal of general physiology, 1983