Modulation of membrane channel currents by gap junction protein mimetic peptides: Size matters

Junjie Wang, Meiyun Ma, Silviu Locovei, Robert Keane, Gerhard Dahl

Research output: Contribution to journalArticle

145 Citations (Scopus)

Abstract

Connexin mimetic peptides are widely used to assess the contribution of nonjunctional connexin channels in several processes, including ATP release. These peptides are derived from various connexin sequences and have been shown to attenuate processes downstream of the putative channel activity. Yet so far, no documentation of effects of peptides on connexin channels has been presented. We tested several connexin and pannexin mimetic peptides and observed attenuation of channel currents that is not compatible with sequence specific actions of the peptides. Connexin mimetic peptides inhibited pannexin channel currents but not the currents of the channel formed by connexins from which the sequence was derived. Pannexin mimetic peptides did inhibit pannexin channel currents but also the channels formed by connexin 46. The same pattern of effects was observed for dye transfer, except that the inhibition levels were more pronounced than for the currents. The channel inhibition by peptides shares commonalities with channel effects of polyethylene glycol (PEG), suggesting a steric block as a mechanism. PEG accessibility is in the size range expected for the pore of innexin gap junction channels, consistent with a functional relatedness of innexin and pannexin channels.

Original languageEnglish
JournalAmerican Journal of Physiology - Cell Physiology
Volume293
Issue number3
DOIs
StatePublished - Sep 1 2007

Fingerprint

Connexins
Ion Channels
Modulation
Peptides
Gap Junctions
Documentation
Coloring Agents
Adenosine Triphosphate

Keywords

  • Calcium wave
  • Mimetic peptide
  • Polyethylene glycol

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Cell Biology
  • Physiology

Cite this

Modulation of membrane channel currents by gap junction protein mimetic peptides : Size matters. / Wang, Junjie; Ma, Meiyun; Locovei, Silviu; Keane, Robert; Dahl, Gerhard.

In: American Journal of Physiology - Cell Physiology, Vol. 293, No. 3, 01.09.2007.

Research output: Contribution to journalArticle

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