Spherical nanosized focal spot unravels the interior of cells.

@article{citeulike:2837703, abstract = {The resolution of any linear imaging system is given by its point spread function (PSF) that quantifies the blur of an object point in the image. The sharper the PSF, the better the resolution is. In standard fluorescence microscopy, however, diffraction dictates a PSF with a cigar-shaped main maximum, called the focal spot, which extends over at least half the wavelength of light (lambda = 400-700 nm) in the focal plane and >lambda along the optical axis (z). Although concepts have been developed to sharpen the focal spot both laterally and axially, none of them has reached their ultimate goal: a spherical spot that can be arbitrarily downscaled in size. Here we introduce a fluorescence microscope that creates nearly spherical focal spots of 40-45 nm (lambda/16) in diameter. Fully relying on focused light, this lens-based fluorescence nanoscope unravels the interior of cells noninvasively, uniquely dissecting their sub-lambda-sized organelles.}, address = {Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37077 G\"{o}ttingen, Germany.}, author = {Schmidt, Roman and Wurm, Christian A A. and Jakobs, Stefan and Engelhardt, Johann and Egner, Alexander and Hell, Stefan W W. }, citeulike-article-id = {2837703}, doi = {http://dx.doi.org/10.1038/nmeth.1214}, issn = {1548-7105}, journal = {Nature methods}, keywords = {super-resolution}, month = {May}, posted-at = {2008-05-29 23:54:00}, priority = {2}, title = {Spherical nanosized focal spot unravels the interior of cells.}, url = {http://dx.doi.org/10.1038/nmeth.1214}, year = {2008} }

TY - JOUR ID - citeulike:2837703 L3 - citeulike-article-id:2837703 TI - Spherical nanosized focal spot unravels the interior of cells. JF - Nature methods AD - Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37077 Göttingen, Germany. SN - 1548-7105 N2 - The resolution of any linear imaging system is given by its point spread function (PSF) that quantifies the blur of an object point in the image. The sharper the PSF, the better the resolution is. In standard fluorescence microscopy, however, diffraction dictates a PSF with a cigar-shaped main maximum, called the focal spot, which extends over at least half the wavelength of light (lambda = 400-700 nm) in the focal plane and >lambda along the optical axis (z). Although concepts have been developed to sharpen the focal spot both laterally and axially, none of them has reached their ultimate goal: a spherical spot that can be arbitrarily downscaled in size. Here we introduce a fluorescence microscope that creates nearly spherical focal spots of 40-45 nm (lambda/16) in diameter. Fully relying on focused light, this lens-based fluorescence nanoscope unravels the interior of cells noninvasively, uniquely dissecting their sub-lambda-sized organelles. KW - super-resolution AU - Schmidt, Roman AU - Wurm, Christian A AU - Jakobs, Stefan AU - Engelhardt, Johann AU - Egner, Alexander AU - Hell, Stefan W PY - 2008/05/18/ UR - http://dx.doi.org/10.1038/nmeth.1214 ER -