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Published March 13, 2012 | Published + Supplemental Material
Journal Article Open

Single-Cell Census of Mechanosensitive Channels in Living Bacteria

Abstract

Bacteria are subjected to a host of different environmental stresses. One such insult occurs when cells encounter changes in the osmolarity of the surrounding media resulting in an osmotic shock. In recent years, a great deal has been learned about mechanosensitive (MS) channels which are thought to provide osmoprotection in these circumstances by opening emergency release valves in response to membrane tension. However, even the most elementary physiological parameters such as the number of MS channels per cell, how MS channel expression levels influence the physiological response of the cells, and how this mean number of channels varies from cell to cell remain unanswered. In this paper, we make a detailed quantitative study of the expression of the mechanosensitive channel of large conductance (MscL) in different media and at various stages in the growth history of bacterial cultures. Using both quantitative fluorescence microscopy and quantitative Western blots our study complements earlier electrophysiology-based estimates and results in the following key insights: i) the mean number of channels per cell is much higher than previously estimated, ii) measurement of the single-cell distributions of such channels reveals marked variability from cell to cell and iii) the mean number of channels varies under different environmental conditions. The regulation of MscL expression displays rich behaviors that depend strongly on culturing conditions and stress factors, which may give clues to the physiological role of MscL. The number of stress-induced MscL channels and the associated variability have far reaching implications for the in vivo response of the channels and for modeling of this response. As shown by numerous biophysical models, both the number of such channels and their variability can impact many physiological processes including osmoprotection, channel gating probability, and channel clustering.

Additional Information

© 2012 Bialecka-Fornal et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Received August 5, 2011; Accepted February 9, 2012; Published March 13, 2012. Editor: Arnold Driessen, University of Groningen, Netherlands. Funding: RP, MBF, and HJL were supported by National Institutes of Health (NIH) grant R01 GM084211 and NIH Director's Pioneer Award grant DP1 OD000217. MBF was supported by a Caltech Provost's office fellowship. HAD was supported by a National Science Foundation graduate research fellowship and the physiology course at the Marine Biology Laboratory in Woods Hole, Massachusetts. CSG was supported by NIH grant R01 GM084211. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We would like to thank Doug Rees, Ian R. Booth, KC Huang, Liz Haswell, Rob Brewster, Troy Walton, Hernan Garcia, Paul Wiggins, Zhenfeng Liu, Tristan Ursell, and Kira Veley for many helpful comments and discussions; the physiology course and its attendees at the Marine Biology Laboratory in Woods Hole, MA for providing the equipment and overall intellectual environment that was the inspiration for this work; Akiko Rasmussen for performing valuable electrophysiology measurements; and Samantha Miller, Susan Black, Troy Walton, Hernan Garcia, and the CGSC at Yale University for materials and technical expertise. Author Contributions: Conceived and designed the experiments: MBF HJL HAD CSG RP. Performed the experiments: MBF HJL HAD . Analyzed the data: MBF HJL HAD . Contributed reagents/materials/analysis tools: MBF HJL HAD CSG RP. Wrote the paper: MBF HJL HAD CSG RP.

Attached Files

Published - BialeckaFornal2012p18154PLoS_ONE.pdf

Supplemental Material - FigS1.tif

Supplemental Material - FigS10.tif

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Supplemental Material - SupportingInfoS1.doc

Supplemental Material - TableS1.doc

Supplemental Material - TableS2.doc

Supplemental Material - TableS3.doc

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Additional details

Created:
August 19, 2023
Modified:
October 17, 2023