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

Author:

Wang Yong12,Liu Yanxin12,DeBerg Hannah A12,Nomura Takeshi3,Hoffman Melinda Tonks12,Rohde Paul R3,Schulten Klaus12,Martinac Boris34,Selvin Paul R125

Affiliation:

1. Department of Physics, University of Illinois at Urbana-Champaign, Urbana, United States

2. Center for the Physics of Living Cells, University of Illinois at Urbana-Champaign, Urbana, United States

3. Molecular Cardiology and Biophysics Division, Victor Chang Cardiac Research Institute, Sydney, Australia

4. St Vincent’s Clinical School, Faculty of Medicine, University of New South Wales, Sydney, Australia

5. Center for Biophysics and Computational Biology, University of Illinois at Urbana-Champaign, Urbana, United States

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.

Funder

National Institutes of Health

National Science Foundation

National Health and Medical Research Council

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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