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Cross-linking of cardiac gap junction connexons by thiol/disulfide exchanges.

Authors
  • Dupont, E
  • el Aoumari, A
  • Briand, J P
  • Fromaget, C
  • Gros, D
Type
Published Article
Journal
The Journal of membrane biology
Publication Date
Jun 01, 1989
Volume
108
Issue
3
Pages
247–252
Identifiers
PMID: 2550652
Source
Medline
License
Unknown

Abstract

SDS-polyacrylamide gel electrophoresis and immunoblotting were used to investigate inter- and intramolecular disulfide bonds to connexin 43 (the cardiac gap junctional protein) in isolated rat heart gap junctions and in whole heart fractions. In gap junctions isolated in the absence of alkylating agent, connexin 43 molecules are cross-linked by disulfide bonds. The use of iodoacetamide (100 mM) for the first steps of isolation procedure prevents the formation of these artifactual linkages. Investigation of connexin 43 in whole heart fractions by means of antibodies confirms the results obtained with isolated gap junctions; that is, connexin 43 molecules are not interconnected with disulfide bridges. In whole heart fractions treated with alkylating agents, a 38 kD protein, immunologically related to connexin 43, and containing intramolecular disulfide bonds is detected. It is hypothesized that this protein might be a folded form of connexin 43, a precursory form of the molecules embedded in the gap junctions.

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