Stimulated Emission Depletion (STED) Microscopy Literature References
STED is based on non-linear optical effects that typically require the application of multiple high-intensity pulsed lasers with specialized modulation filters to control the excitation beam geometry (a technique commonly termed point-spread function engineering). The excessively high cost of pulsed lasers has been addressed with the introduction of CW-STED systems that implement lower cost continuous wave lasers. Even though point-spread function modifying schemes are capable of achieving lateral resolution measured in the tens of nanometers, these methods can potentially damage specimens with high levels of excitation light and require fluorescent probes that are resistant to photobleaching. Furthermore, they rely on highly complex and specialized microscope configurations that are difficult for the average cell biologist to assemble.
Recommended Literature
- Donnert, G., Keller, J., Wurm, C. A., Rizzoli, S. O., Westphal, V., Schonle, A., Jahn, R., Jakobs, S., Eggeling, C. and Hell, S. W. Two-color far-field fluorescence nanoscopy. Biophysical Journal 92: L67-L69 (2007).
- Dyba, M. and Hell, S. W. Focal spots of size wavelength/23 open up far-field florescence microscopy at 33 nm axial resolution. Physical Review Letters 88: 163901-4 (2002).
- Dyba, M., Jakobs, S. and Hell, S. W. Immunofluorescence stimulated emission depletion microscopy. Nature Biotechnology 21: 1303-1304 (2003).
- Folling, J., Belov, V., Riedel, D., Schonle, A., Egner, A., Eggeling, C., Bossi, M. and Hell, S. W. Fluorescence nanoscopy with optical sectioning by two-photon induced molecular switching using continuous-wave lasers. ChemPhysChem 9: 321-326 (2008).
- Hein, B., Willig, K. L. and Hell, S. W. Stimulated emission depletion (STED) nanoscopy of a fluorescent protein-labeled organelle inside a living cell. Proceedings of the National Academy of Sciences (USA) 105: 14271-14276 (2008).
- Hell, S. W. Increasing the resolution of far-field fluorescence light microscopy by point-spread-function engineering. Topics in Fluorescence Spectroscopy 5: 361-426 (2002).
- Hell, S. W. and Wichmann, J. Breaking the diffraction resolution limit by stimulated emission: Stimulated-emission-depletion fluorescence microscopy. Optics Letters 19:780-782 (1994).
- Hoffman, M., Eggeling, C., Jakobs, S. and Hell, S. W. Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins. Proceedings of the National Academy of Sciences (USA) 102: 17565-17569 (2005).
- Kasper, R., Harke, B., Forthmann, C., Tinnefeld, P., Hell, S. W. and Sauer, M. Single-molecule STED microscopy with photostable organic fluorophores. Small 6: 1379-1384 (2010).
- Klar, T. A., Engel, E. and Hell, S. W. Breaking Abbe's diffraction resolution limit in fluorescence microscopy with stimulated emission depletion beams of various shapes.Physical Review E 64: 066613-9 (2001).
- Klar, T. A., Jakobs, S., Dyba, M., Egner, A. and Hell, S. Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission. Proceedings of the National Academy of Sciences (USA) 97: 8206-8210 (2000).
- Meyer, L., Wildanger, D., Medda, R., Punge, A., Rizzoli, S. O., Donnert, G. and Hell, S. W. Dual-color STED microscopy at 30-nm focal-plane resolution. Small 4: 1095-1100 (2008).
- Moneron, G. and Hell, S. W. Two-photon excitation STED microscopy. Optics Express 17:14567-14573 (2009).
- Nagerl, U. V., Willig, K. I., Hein, B., Hell, S. W. and Bonhoeffer, T. Live-cell imaging of dendritic spines by STED microscopy. Proceedings of the National Academy of Sciences (USA)105: 18982-18987 (2008).
- Schmidt, R., Wurm, C. A., Jakobs, S., Engelhardt, J., Egner, A. and Hell, S. W. Spherical nanosized focal spot unravels the interior of cells. Nature Methods 5: 539-544 (2008).
- Schmidt, R., Wurm, C. A., Punge, A., Egner, A., Jakobs, S. and Hell, S. W. Mitochondrial cristae revealed with focused light. Nano Letters 9: 2508-2510 (2009).
- Westphal, V. and Hell, S. W. Nanoscale resolution in the focal plane of an optical microscope. Physical Review Letters 94: 143903-4 (2005).
- Westphal, V., Rizzoli, S. O., Lauterbach, M. A., Kamin, D., Jahn, R. and Hell, S.W. Video-rate far-field optical nanoscopy dissects synaptic vesicle movement. Science 320: 246-249 (2008).
- Wildanger, D., Medda, R., Kastrup, L. and Hell, S. W. A compact STED microscope providing 3D nanoscale resolution. Journal of Microscopy 236: 35-43 (2009).
- Wildanger, D., Rittweger, E., Kastrup, L. and Hell, S. W. STED microscopy with a supercontinuum laser source. Optics Express 16: 9614-9621 (2008).
- Willig, K. I., Harke, B., Medda, R. and Hell, S. W. STED microscopy with continuous wave beams. Nature Methods 4: 915-918 (2007).
- Willig, K. I., Keller, J., Bossi, M. and Hell, S. W. STED microscopy resolves nanoparticle assemblies. New Journal of Physics 8: 106 (2006).
- Willig, K. I., Kellner, R. R., Medda, R., Hein, B., Jakobs, S. and Hell, S. W. Nanoscale resolution in GFP-based microscopy. Nature Methods 3: 721-723 (2006).
- Willig, K. I., Rizzoli, S. O., Westphal, V., Jahn, R. and Hell, S. W. STED microscopy reveals that synaptotagmin remains clustered after synaptic vesicle exocytosis. Nature 440: 935-939 (2006).
Additional Literature Sources
- Avidan, A. and Oron, D. Sub-diffraction limited imaging with fluorophores exhibiting emission depletion upon saturation. Optics Express 17: 963-969 (2009).
- Belfield, K. D., Bondar, M. V., Yanez, C. O., Hernandez, F. E. and Przhonska, O. V. One- and two-photon stimulated emission depletion of a sulfonyl-containing fluorene derivative.Journal of Physical Chemistry B 113: 7101-7106 (2009).
- Cseresnyes, Z., Schwarz, U. and Green, C. M. Analysis of replication factories in human cells by super-resolution light microscopy. BMC Cell Biology 10: 88 (2009).
- Dedecker, P., Hotta, J., Flors, C., Sliwa, M., Uji-i, H., Roeffaers, M. B. J., Ando, R., Mizuno, H., Miyawaki, A. and Hofkens, J. Subdiffraction imaging through the selective donut-mode depletion of thermally stable photoswitchable fluorophores: Numerical analysis and application to the fluorescent protein Dronpa. Journal of the American Chemical Society129: 16132-16141 (2007).
- Deng, Y. and Shaevitz, J. W. Effect of aberration on height calibration in three-dimensional localization-based microscopy and particle tracking. Applied Optics 48: 1886-1890 (2009).
- Ding, J. B., Takasaki, K. T. and Sabatini, B. L. Supraresolution imaging in brain slices using stimulated-emission depletion two-photon laser scanning microscopy. Neuron 63: 429-437 (2009).
- Dyba, M. and Hell, S. W. Photostability of a fluorescent marker under pulsed excited-state depletion through stimulated emission. Applied Optics 42: 5123-5129 (2003).
- Eggeling, C., Ringemann, C., Medda, R., Schwarzmann, G., Sandhoff, K., Polyakova, S., Belov, V. N., Hein, B., von Middendorff, C., Schonle, A. and Hell, S. W. Direct observation of the nanoscale dynamics of membrane lipids in a living cell. Nature 457: 1159-1162 (2009).
- Evanko, D. STEDy progress. Nature Methods 3: 661 (2006).
- Fitzpatrick, J. A. J., Yan, Q., Sieber, J. J., Dyba, M., Schwarz, U., Szent-Gyorgyi, C., Woolford, C. A., Berget, P. B., Waggoner, A. S. and Bruchez, M. P. STED nanoscopy in living cells using fluorogen activating proteins. Bioconjugate Chemistry 20: 1843-1847 (2009).
- Flors, C. Photoswitching of monomeric and dimeric DNA-intercalating cyanine dyes for super-resolution microscopy applications. Photochemical and Photobiological Sciences9: 643-648 (2010).
- Flors, C., Ravarani, C. N. J. and Dryden, D. T. F. Super-resolution imaging of DNA labelled with intercalating dyes. ChemPhysChem 10: 2201-2204 (2009).
- Han, K. Y., Willig, K. I., Rittweger, E., Jelezko, F., Eggeling, C. and Hell, S. W. Three-dimensional stimulated emission depletion microscopy of nitrogen-vacancy centers in diamond using continuous-wave light. Nano Letters 9: 3323-3329 (2009).
- Harke, B., Keller, J., Ullal, C. K., Westphal, V., Schonle, A. and Hell, S. W. Resolution scaling in STED microscopy. Optics Express 16: 4154-4162 (2008).
- Harke, B., Ullal, C. K., Keller, J. and Hell, S. W. Three-dimensional nanoscopy of colloidal crystals. Nano Letters 8: 1309-1313 (2008).
- Hein, B., Willig, K. L., Wurm, C. A., Westphal, V., Jakobs, S. and Hell, S. W. Stimulated emission depletion nanoscopy of living cells using SNAP-tag fusion proteins. Biophysical Journal 98: 158-163 (2010).
- Hell, S. W. Improvement of lateral resolution in far-field fluorescence light microscopy by using two-photon excitation with offset beams. Optics Communications 106: 19-24 (1994).
- Hotta, J., Fron, E., Dedecker, P., Janssen, K. P. F., Li, C., Mullen, K., Harke, B., Buckers, J., Hell, S. W. and Hofkens, J. Spectroscopic rationale for efficient stimulated-emission depletion microscopy fluorophores. Journal of the American Chemical Society 132: 5021-5023 (2010).
- Kamin, D., Lauterbach, M. A., Westphal, V., Keller, J., Schonle, A., Hell, S. W. and Rizzoli, S. O.High- and low-mobility stages in the synaptic vesicle cycle. Biophysical Journal 99: 675-684 (2010).
- Kellner, R. R., Baier, C. J., Willig, K. I., Hell, S. W. and Barrantes, F. J. Nanoscale organization of nicotinic acetylcholine receptors revealed by stimulated emission depletion microscopy. Neuroscience 144: 135-143 (2007).
- Kittel, R. J., Wichmann, C., Rasse, T. M., Fouquet, W., Schmidt, M., Schmid, A., Wagh, D. A., Pawlu, C., Kellner, R. R., Willig, K. I., Hell, S. W., Buchner, E., Heckmann, M. and Sigrist, S. J. Bruchpilot promotes active zone assembly, Ca2+ channel clustering, and vesicle release.Science 312: 1051-1054 (2006).
- Kuang, C., Zhao, W. and Wang, G. Far-field optical nanoscopy based on continuous wave laser stimulated emission depletion. Review of Scientific Instruments 81: 053709-4 (2010).
- Lauterbach, M. A., Keller, J., Schonle, A., Kamin, D., Westphal, V., Rizzoli, S. O. and Hell, S. W.Comparing video-rate STED nanoscopy and confocal microscopy of living neurons.Journal of Biophotonics 3: 417-424 (2010).
- Li, Q., Wu, S. S. H. and Chou, K. C. Subdiffraction-limit two-photon fluorescence microscopy for GFP-tagged cell imaging. Biophysical Journal 97: 3224-3228 (2009).
- Moneron, G., Medda, R., Hein, B., Giske, A., Westphal, V. and Hell, S. W. Fast STED microscopy with continuous wave fiber lasers. Optics Express 18: 1302-1309 (2010).
- Neumann, D., Buckers, J., Kastrup, L., Hell, S. W. and Jakobs, S. Two-color STED microscopy reveals different degrees of colocalization between hexokinase-I and the three human VDAC isoforms. BMC Biophysics 3: 4 (2010).
- Punge, A., Rizzoli, S. O., Jahn, R., Wildanger, J. D., Meyer, L., Schonle, A., Kastrup, L. and Hell, S. W. 3D reconstruction of high-resolution STED microscope images. Microscopy Research and Technique 71: 644-650 (2008).
- Rankin, B. R. and Hell, S. W. STED microscopy with a MHz pulsed stimulated-Raman-scattering source. Optics Express 17: 15679-15684 (2009).
- Reuss, M., Engelhardt, J. and Hell, S. W. Birefringent device converts a standard scanning microscope into a STED microscope that also maps molecular orientation. Optics Express18: 1049-1058 (2010).
- Sahl, S. J., Leutenegger, M., Hilbert, M., Hell, S. W. and Eggeling, C. Fast molecular tracking maps nanoscale dynamics of plasma membrane lipids. Proceedings of the National Academy of Science of the United States of America 107: 6829-6834 (2010).
- Schneider, A., Rajendran, L., Honsho, M., Gralle, M., Donnert, G., Wouters, F., Hell, S. W. and Simons, M. Flotillin-dependent clustering of the amyloid precursor protein regulates its endocytosis and amyloidogenic processing in neurons. Journal of Neuroscience 28: 2874-2882 (2008).
- Schroder, J., Benink, H., Dyba, M. and Los, G. V. In vivo labeling method using a genetic construct for nanoscale resolution microscopy. Biophysical Journal 96: L1-L3 (2009).
- Sieber, J. J., Willig, K. I., Heintzmann, R., Hell, S. W. and Lang, T. The SNARE motif is essential for the formation of syntaxin clusters in the plasma membrane. Biophysical Journal 90: 2843-2851 (2006).
- Sieber, J. J., Willig, K. I., Kutzner, C., Gerding-Reimers, C., Harke, B., Donnert, G., Rammner, B., Eggeling, C., Hell, S. W., Grubmuller, H. and Lang, T. Anatomy and dynamics of a supramolecular membrane protein cluster. Science 317: 1072-1076 (2007).
- Torok, P. and Munro, P. The use of Gauss-Laguerre vector beams in STED microscopy.Optics Express 12: 3605-3617 (2004).
- Ullal, C. K., Schmidt, R., Hell, S. W. and Egner, A. Block copolymer nanostructures mapped by far-field optics. Nano Letters 9: 2497-2500 (2009).
- Watanabe, T., Iketaki, Y., Omatsu, T., Yamamoto, K., Ishiuchi, S. I., Sakai, M. and Fujii, M. Two-color far-field super-resolution microscope using a doughnut beam. Chemical Physics Letters 371: 634-639 (2003).
- Westphal, V., Blanca, C. M., Dyba, M., Kastrup, L. and Hell, S. W. Laser-diode-stimulated emission depletion microscopy. Applied Physics Letters 82: 3125-3127 (2003).
- Westphal, V., Kastrup, L. and Hell, S. W. Lateral resolution of 28 nm (wavelength/25) in far-field fluorescence microscopy. Applied Physics B Lasers and Optics 77: 377-380 (2003).
- Wildanger, D., Buckers, J., Westphal, V., Hell, S. W. and Kastrup, L. A STED microscope aligned by design. Optics Express 17: 16100-16110 (2009).