Conductance mutations of the nicotinic acetylcholine receptor do not act by a simple electrostatic mechanism

Biophys J. 1994 Feb;66(2 Pt 1):325-34. doi: 10.1016/s0006-3495(94)80781-7.

Abstract

Fixed negative charges in many cation channels raise the single-channel conductance, apparently by an electrostatic mechanism: their effects are accentuated in solutions of low ionic strength and attenuated at high ionic strength. The charges of specific amino acids near the ends of the proposed pore-lining M2 segment of the nicotinic acetylcholine receptor, termed the extracellular and cytoplasmic rings, have recently been shown to influence the single-channel K+ conductance (Imoto, K., C. Busch, B. Sakmann, M. Mishina, T. Konno, J. Nakai, H. Bujo, Y. Mori, K. Fukuda and S. Numa. 1988. Nature 335:645-648). We examined whether these charges might act by a direct electrostatic effect on the energy of ions in the pore, rather than indirectly by inducing a structural change. To this end, we measured the conductances of charge mutants over a range of K+ concentrations (ionic strengths). As expected, we found that negative charge mutations raise the conductance, and positive charge mutations lower it. The effects of cytoplasmic-ring mutations are accentuated at low ionic strength, but they are not completely attenuated at high ionic strength. The effects of extracellular-ring mutations are independent of ionic strength. These results are inconsistent with the simplest electrostatic model. We suggest a modified model that qualitatively accounts for the data.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Biophysical Phenomena
  • Biophysics
  • Electric Conductivity
  • Electrochemistry
  • Female
  • In Vitro Techniques
  • Kinetics
  • Magnesium / pharmacology
  • Mice
  • Models, Chemical
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Osmolar Concentration
  • Potassium / metabolism
  • Receptors, Nicotinic / chemistry*
  • Receptors, Nicotinic / genetics*
  • Receptors, Nicotinic / metabolism
  • Thermodynamics
  • Xenopus laevis

Substances

  • Receptors, Nicotinic
  • Magnesium
  • Potassium