TY - JOUR
T1 - Optical tweezers assisted imaging of the Z-ring in Escherichia coli
T2 - Measuring its radial width
AU - Carmon, G.
AU - Kumar, P.
AU - Feingold, M.
PY - 2014/1
Y1 - 2014/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84894155212&partnerID=8YFLogxK
U2 - 10.1088/1367-2630/16/1/013043
DO - 10.1088/1367-2630/16/1/013043
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AN - SCOPUS:84894155212
SN - 1367-2630
VL - 16
JO - New Journal of Physics
JF - New Journal of Physics
M1 - 013043
ER -