Tracking of single fluorescent particles in three dimensions: use of cylindrical optics to encode particle position Export

@misc{DOI - 10.1016/S0006-3495(94)80601-0, abstract = {We present a novel optical technique for three-dimensional tracking of single fluorescent particles using a modified epifluorescence microscope containing a weak cylindrical lens in the detection optics and a microstepper-controlled fine focus. Images of small, fluorescent particles were circular in focus but ellipsoidal above and below focus; the major axis of the ellipsoid shifted by 90 degrees in going through focus. Particle z position was determined from the image shape and orientation by applying a peak detection algorithm to image projections along the x and y axes; x, y position was determined from the centroid of the particle image. Typical spatial resolution was 12 nm along the optical axis and 5 nm in the image plane with a maximum sampling rate of 34 Hz. The method was applied to track fluorescent particles in artificial solutions and living cells. In a solution of viscosity 30 cP, the mean squared distance (MSD) traveled by a 264 nm diameter rhodamine-labeled bead was linear with time to 20 s. The measured diffusion coefficient, 0.0558 +/- 0.001 micron2/s (SE, n = 4), agreed with the theoretical value of 0.0556 micron2/s. Statistical variability of MSD curves for a freely diffusing bead was in quantitative agreement with Monte Carlo simulations of three-dimensional random walks. In a porous glass matrix, the MSD data was curvilinear and showed reduced bead diffusion. In cytoplasm of Swiss 3T3 fibroblasts, bead diffusion was restricted. The water permeability in individual Chinese Hamster Ovary cells was measured from the z movement of a fluorescent bead fixed at the cell surface in response osmotic gradients; water permeability was increased by > threefold in cells expressing CHIP28 water channels. The simplicity and precision of this tracking method may be useful to quantify the complex trajectories of fluorescent particles in living cells.}, author = {Kao, H. P. and Verkman, A. S.}, citeulike-article-id = {4860372}, citeulike-linkout-0 = {http://linkinghub.elsevier.com/retrieve/pii/S0006349594806010}, day = {1}, issn = {0006-3495}, keywords = {3d, microscopy, tracking-diffusion}, month = {September}, number = {3}, pages = {1291--1300}, posted-at = {2009-06-15 15:44:33}, priority = {2}, title = {Tracking of single fluorescent particles in three dimensions: use of cylindrical optics to encode particle position}, url = {http://linkinghub.elsevier.com/retrieve/pii/S0006349594806010}, volume = {67}, year = {1994} }

TY - ABST ID - DOI - 10.1016/S0006-3495(94)80601-0 L3 - citeulike-article-id:4860372 N2 - We present a novel optical technique for three-dimensional tracking of single fluorescent particles using a modified epifluorescence microscope containing a weak cylindrical lens in the detection optics and a microstepper-controlled fine focus. Images of small, fluorescent particles were circular in focus but ellipsoidal above and below focus; the major axis of the ellipsoid shifted by 90 degrees in going through focus. Particle z position was determined from the image shape and orientation by applying a peak detection algorithm to image projections along the x and y axes; x, y position was determined from the centroid of the particle image. Typical spatial resolution was 12 nm along the optical axis and 5 nm in the image plane with a maximum sampling rate of 34 Hz. The method was applied to track fluorescent particles in artificial solutions and living cells. In a solution of viscosity 30 cP, the mean squared distance (MSD) traveled by a 264 nm diameter rhodamine-labeled bead was linear with time to 20 s. The measured diffusion coefficient, 0.0558 +/- 0.001 micron2/s (SE, n = 4), agreed with the theoretical value of 0.0556 micron2/s. Statistical variability of MSD curves for a freely diffusing bead was in quantitative agreement with Monte Carlo simulations of three-dimensional random walks. In a porous glass matrix, the MSD data was curvilinear and showed reduced bead diffusion. In cytoplasm of Swiss 3T3 fibroblasts, bead diffusion was restricted. The water permeability in individual Chinese Hamster Ovary cells was measured from the z movement of a fluorescent bead fixed at the cell surface in response osmotic gradients; water permeability was increased by > threefold in cells expressing CHIP28 water channels. The simplicity and precision of this tracking method may be useful to quantify the complex trajectories of fluorescent particles in living cells. IS - 3 SN - 0006-3495 EP - 1300 TI - Tracking of single fluorescent particles in three dimensions: use of cylindrical optics to encode particle position VL - 67 SP - 1291 KW - 3d KW - microscopy KW - tracking-diffusion AU - Kao, HP AU - Verkman, AS PY - 1994/09/01/ UR - http://linkinghub.elsevier.com/retrieve/pii/S0006349594806010 ER -