Actin modifies Ca2+ block of epithelial Na+ channels in planar lipid bilayers

Biophys J. 2001 May;80(5):2176-86. doi: 10.1016/S0006-3495(01)76190-5.


The mechanism by which the cytoskeletal protein actin affects the conductance of amiloride-sensitive epithelial sodium channels (ENaC) was studied in planar lipid bilayers. In the presence of monomeric actin, we found a decrease in the single-channel conductance of alpha-ENaC that did not occur when the internal [Ca2+]free was buffered to <10 nM. An analysis of single-channel kinetics demonstrated that Ca2+ induced the appearance of long-lived closed intervals separating bursts of channel activity, both in the presence and in the absence of actin. In the absence of actin, the duration of these bursts and the time spent by the channel in its open, but not in its short-lived closed state, were inversely proportional to [Ca2+]. This, together with a lengthening of the interburst intervals, translated into a dose-dependent decrease in the single-channel open probability. In contrast, a [Ca2+]-dependent decrease in alpha-ENaC conductance in the presence of actin was accompanied by lengthening of the burst intervals with no significant changes in the open or closed (both short- and long-lived) times. We conclude that Ca2+ acts as a "fast-to-intermediate" blocker when monomeric actin is present, producing a subsequent attenuation of the apparent unitary conductance of the channel.

Publication types

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

MeSH terms

  • Actins / chemistry*
  • Actins / metabolism
  • Animals
  • Biophysical Phenomena
  • Biophysics
  • Calcium / chemistry
  • Calcium / metabolism*
  • Dose-Response Relationship, Drug
  • Epithelial Sodium Channels
  • Kinetics
  • Lipid Bilayers / chemistry*
  • Models, Chemical
  • Muscles / metabolism
  • Protein Conformation
  • Proteolipids / chemistry
  • Rabbits
  • Sodium Channels / chemistry
  • Sodium Channels / metabolism*


  • Actins
  • Epithelial Sodium Channels
  • Lipid Bilayers
  • Proteolipids
  • Sodium Channels
  • proteoliposomes
  • Calcium