GTP-binding proteins couple cardiac muscarinic receptors to a K channel

Nature. 1985 Oct 10-16;317(6037):536-8. doi: 10.1038/317536a0.


Binding of acetylcholine (ACh) to cardiac muscarinic ACh receptors (mAChR) activates a potassium channel that slows pacemaker activity. Although the time course of this activation suggests a multi-step process with intrinsic delays of 30-100 ms, no second-messenger system has been demonstrated to link the mAChR to the channel. Changes in cyclic nucleotide levels (cyclic AMP and cyclic GMP) do not affect this K channel or its response to muscarinic agonists. Indeed, electrophysiological experiments argue against the involvement of any second messenger that diffuses through the cytoplasm. We report here that coupling of the mAChR in embryonic chick atrial cells to this inward rectifying K channel requires intracellular GTP. Furthermore, pretreatment of cells with IAP (islet-activating protein from the bacterium Bordetella pertussis) eliminates the ACh-induced inward rectification. As IAP specifically ADP-ribosylates two GTP-binding proteins, Ni and No, that can interact with mAChRs, we conclude that a guanyl nucleotide-binding protein couples ACh binding to channel activation. This represents the first demonstration that a GTP-binding protein can regulate the function of an ionic channel without acting through cyclic nucleotide second messengers.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylcholine / metabolism
  • Animals
  • Chick Embryo
  • Electrophysiology
  • GTP-Binding Proteins / metabolism*
  • Guanosine Triphosphate / metabolism
  • Ion Channels / physiology*
  • Pertussis Toxin
  • Potassium / metabolism*
  • Receptors, Muscarinic / metabolism*
  • Virulence Factors, Bordetella / metabolism


  • Ion Channels
  • Receptors, Muscarinic
  • Virulence Factors, Bordetella
  • Guanosine Triphosphate
  • Pertussis Toxin
  • GTP-Binding Proteins
  • Acetylcholine
  • Potassium