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Biophys J, September 2001, p. 1406-1418, Vol. 81, No. 3


and
*Krannert Institute of Cardiology, Indiana University,
Indianapolis, Indiana 46202;
Department of Pediatrics,
University of Chicago, Chicago, Illinois 60637; and
Department of Pharmacology, State University of New York
Upstate Medical University, Syracuse, New York USA
Immunohistochemical co-localization of distinct connexins
(Cxs) in junctional areas suggests the formation of heteromultimeric channels. To determine the docking effects of the heterotypic combination of Cx43 and Cx45 on the voltage-gating properties of their
channels, we transfected DNA encoding Cx43 or Cx45 into N2A
neuroblastoma or HeLa cells. Using a double whole-cell voltage-clamp technique, we determined macroscopic and single-channel gating properties of the intercellular channels formed. Cx43-Cx45 heterotypic channels had rectifying properties where Cx45 connexons inactivated rapidly upon hyperpolarizing voltage pulses applied to the
Cx45-expressing cell. During depolarizing pulses to the Cx45-expressing
cell, Cx43 connexons inactivated with substantially reduced kinetics as
compared with homotypic Cx43 channels. Similar slow kinetics was
observed for homotypic Cx43M257 (truncation mutant). Heterotypic channels had a main conductance whose value was predicted by the sum of
corresponding homomeric connexon conductances; it was not voltage
dependent and had no detectable residual conductance. The
voltage-gating kinetics of heterotypic channels and their single-channel behavior implicate a role for the Cx43 carboxyl-terminal domain in the fast gating mechanism and in the establishment of residual conductance. Our results also suggest that heterotypic docking
may lead to conformational changes that inhibit this action of the Cx43
carboxyl-terminal domain.
Biophys J, September 2001, p. 1406-1418, Vol. 81, No. 3
© 2001 by the Biophysical Society 0006-3495/01/09/1406/13 $2.00
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