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Super-resolution photon-efficient imaging by nanometric double-helix point spread function localization of emitters (SPINDLE)Ginni Grover, Keith DeLuca, Sean Quirin, Jennifer DeLuca, and Rafael Piestun »View Author Affiliations
Ginni Grover,1,*
Keith DeLuca,2
Sean Quirin,1
Jennifer DeLuca,2
and Rafael Piestun1
1Department of Electrical, Computer and Energy Engineering, University of Colorado, Boulder, Colorado, 80309, USA 2Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado, 80523, USA *Corresponding author: Ginni.Grover@colorado.edu |
Optics Express, Vol. 20, Issue 24, pp. 26681-26695 (2012)
http://dx.doi.org/10.1364/OE.20.026681
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Abstract
Super-resolution imaging with photo-activatable or photo-switchable probes is a promising tool in biological applications to reveal previously unresolved intra-cellular details with visible light. This field benefits from developments in the areas of molecular probes, optical systems, and computational post-processing of the data. The joint design of optics and reconstruction processes using double-helix point spread functions (DH-PSF) provides high resolution three-dimensional (3D) imaging over a long depth-of-field. We demonstrate for the first time a method integrating a Fisher information efficient DH-PSF design, a surface relief optical phase mask, and an optimal 3D localization estimator. 3D super-resolution imaging using photo-switchable dyes reveals the 3D microtubule network in mammalian cells with localization precision approaching the information theoretical limit over a depth of 1.2 µm.
© 2012 OSA
OCIS Codes
(110.4850) Imaging systems : Optical transfer functions
(170.3880) Medical optics and biotechnology : Medical and biological imaging
(180.2520) Microscopy : Fluorescence microscopy
(180.6900) Microscopy : Three-dimensional microscopy
(110.1758) Imaging systems : Computational imaging
(050.4865) Diffraction and gratings : Optical vortices
ToC Category:
Imaging Systems
History
Original Manuscript: August 6, 2012
Revised Manuscript: October 16, 2012
Manuscript Accepted: November 5, 2012
Published: November 12, 2012
Virtual Issues
Vol. 7, Iss. 12 Virtual Journal for Biomedical Optics
Citation
Ginni Grover, Keith DeLuca, Sean Quirin, Jennifer DeLuca, and Rafael Piestun, "Super-resolution photon-efficient imaging by nanometric double-helix point spread function localization of emitters (SPINDLE)," Opt. Express 20, 26681-26695 (2012)
http://www.opticsinfobase.org/vjbo/abstract.cfm?URI=oe-20-24-26681
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References
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- K. I. Mortensen, L. S. Churchman, J. A. Spudich, and H. Flyvbjerg, “Optimized localization analysis for single-molecule tracking and super-resolution microscopy,” Nat. Methods 7(5), 377–381 (2010). [CrossRef] [PubMed]
- J. Fölling, M. Bossi, H. Bock, R. Medda, C. A. Wurm, B. Hein, S. Jakobs, C. Eggeling, and S. W. Hell, “Fluorescence nanoscopy by ground-state depletion and single-molecule return,” Nat. Methods 5(11), 943–945 (2008). [CrossRef] [PubMed]
- F. Cella Zanacchi, Z. Lavagnino, M. Perrone Donnorso, A. Del Bue, L. Furia, M. Faretta, and A. Diaspro, “Live-cell 3D super-resolution imaging in thick biological samples,” Nat. Methods 8(12), 1047–1049 (2011). [CrossRef] [PubMed]
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- G. Shtengel, J. A. Galbraith, C. G. Galbraith, J. Lippincott-Schwartz, J. M. Gillette, S. Manley, R. Sougrat, C. M. Waterman, P. Kanchanawong, M. W. Davidson, R. D. Fetter, and H. F. Hess, “Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure,” Proc. Natl. Acad. Sci. U.S.A. 106(9), 3125–3130 (2009). [CrossRef] [PubMed]
- D. Aquino, A. Schönle, C. Geisler, C. V. Middendorff, C. A. Wurm, Y. Okamura, T. Lang, S. W. Hell, and A. Egner, “Two-color nanoscopy of three-dimensional volumes by 4Pi detection of stochastically switched fluorophores,” Nat. Methods 8(4), 353–359 (2011). [CrossRef] [PubMed]
- G. Shtengel, J. A. Galbraith, C. G. Galbraith, J. Lippincott-Schwartz, J. M. Gillette, S. Manley, R. Sougrat, C. M. Waterman, P. Kanchanawong, M. W. Davidson, R. D. Fetter, and H. F. Hess, “Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure,” Proc. Natl. Acad. Sci. U.S.A. 106(9), 3125–3130 (2009). [CrossRef] [PubMed]
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- M. F. Juette, T. J. Gould, M. D. Lessard, M. J. Mlodzianoski, B. S. Nagpure, B. T. Bennett, S. T. Hess, and J. Bewersdorf, “Three-dimensional sub-100 nm resolution fluorescence microscopy of thick samples,” Nat. Methods 5(6), 527–529 (2008). [CrossRef] [PubMed]
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Nano Research
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Proc. SPIE
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