Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel

Elife. 2014 Feb 18:3:e01834. doi: 10.7554/eLife.01834.

Abstract

The mechanosensitive channel of large conductance, which serves as a model system for mechanosensitive channels, has previously been crystallized in the closed form, but not in the open form. Ensemble measurements and electrophysiological sieving experiments show that the open-diameter of the channel pore is >25 Å, but the exact size and whether the conformational change follows a helix-tilt or barrel-stave model are unclear. Here we report measurements of the distance changes on liposome-reconstituted MscL transmembrane α-helices, using a 'virtual sorting' single-molecule fluorescence energy transfer. We observed directly that the channel opens via the helix-tilt model and the open pore reaches 2.8 nm in diameter. In addition, based on the measurements, we developed a molecular dynamics model of the channel structure in the open state which confirms our direct observations. DOI: http://dx.doi.org/10.7554/eLife.01834.001.

Keywords: MscL; barrel-stave model; helix-tilt model.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cloning, Molecular
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism*
  • Fluorescence Resonance Energy Transfer / methods*
  • Fluorescent Dyes / metabolism
  • Ion Channel Gating*
  • Ion Channels / chemistry
  • Ion Channels / genetics
  • Ion Channels / metabolism*
  • Kinetics
  • Liposomes
  • Mechanotransduction, Cellular*
  • Membrane Potentials
  • Molecular Dynamics Simulation
  • Mutation
  • Porosity
  • Protein Structure, Secondary
  • Structure-Activity Relationship

Substances

  • Escherichia coli Proteins
  • Fluorescent Dyes
  • Ion Channels
  • Liposomes
  • MscL protein, E coli