Pocket delipidation induced by membrane tension or modification leads to a structurally analogous mechanosensitive channel state

Structure. 2022 Apr 7;30(4):608-622.e5. doi: 10.1016/j.str.2021.12.004. Epub 2022 Jan 4.

Abstract

The mechanosensitive ion channel of large conductance MscL gates in response to membrane tension changes. Lipid removal from transmembrane pockets leads to a concerted structural and functional MscL response, but it remains unknown whether there is a correlation between the tension-mediated state and the state derived by pocket delipidation in the absence of tension. Here, we combined pulsed electron paramagnetic resonance spectroscopy and hydrogen-deuterium exchange mass spectrometry, coupled with molecular dynamics simulations under membrane tension, to investigate the structural changes associated with the distinctively derived states. Whether it is tension- or modification-mediated pocket delipidation, we find that MscL samples a similar expanded subconducting state. This is the final step of the delipidation pathway, but only an intermediate stop on the tension-mediated path, with additional tension triggering further channel opening. Our findings hint at synergistic modes of regulation by lipid molecules in membrane tension-activated mechanosensitive channels.

Keywords: EPR spectroscopy; ESSEM; HDX; MD; MscL; MscS; force-from-lipid; lipids; mass spectrometry; mechanosensitive channels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Escherichia coli / metabolism
  • Escherichia coli Proteins* / chemistry
  • Ion Channels / chemistry
  • Lipid Bilayers / metabolism
  • Molecular Dynamics Simulation

Substances

  • Escherichia coli Proteins
  • Ion Channels
  • Lipid Bilayers
  • MscL protein, E coli