Abstract
Using single-beam, oscillating optical tweezers we can trap and rotate rod-shaped bacterial cells with respect to the optical axis. This technique allows imaging fluorescently labeled three-dimensional sub-cellular structures from different, optimized viewpoints. To illustrate our method we measure D, the radial width of the Z-ring in unconstricted Escherichia coli. We use cells that express FtsZ-GFP and have their cytoplasmic membrane stained with FM4-64. In a vertically oriented cell, both the Z-ring and the cytoplasmic membrane images appear as symmetric circular structures that lend themselves to quantitative analysis. We found that D ≅ 100 nm, much larger than expected. © 2014 IOP Publishing and Deutsche Physikalische Gesellschaft.
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CITATION STYLE
Carmon, G., Kumar, P., & Feingold, M. (2014). Optical tweezers assisted imaging of the Z-ring in Escherichia coli: Measuring its radial width. New Journal of Physics, 16. https://doi.org/10.1088/1367-2630/16/1/013043
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