Quasi-isotropic 3-D resolution in two-photon scanning microscopy.

One of the main challenges in three-dimensional microscopy is to overcome the lack of isotropy of the spatial resolution, which results from the axially-elongated shape of the point spread function. Such anisotropy gives rise to images in which significant axially-oriented structures of the sample are not resolved. In this paper we achieve an important improvement in z resolution in two-photon excitation microscopy through spatial modulation of the incident beam. Specifically, we demonstrate that the design and implementation of a simple shaded ring performs quasi-isotropic threedimensional imaging and that the corresponding loss in luminosity can be easily compensated by most available femtosecond lasers. The outcome looks particularly relevant to nano-fabrication and optical manipulation.

[1]  Tasso R. M. Sales,et al.  Smallest Focal Spot , 1998 .

[2]  S. Hell,et al.  Focal spots of size lambda/23 open up far-field fluorescence microscopy at 33 nm axial resolution. , 2002, Physical review letters.

[3]  Genaro Saavedra,et al.  Optical‐sectioning improvement in two‐color excitation scanning microscopy , 2004, Microscopy research and technique.

[4]  F. Del Bene,et al.  Optical Sectioning Deep Inside Live Embryos by Selective Plane Illumination Microscopy , 2004, Science.

[5]  Jianwei Miao,et al.  High resolution 3-D X-ray diffraction microscopy and its potential of imaging single biomolecules , 2002 .

[6]  Gilbert Boyer,et al.  New class of axially apodizing filters for confocal scanning microscopy. , 2002, Journal of the Optical Society of America. A, Optics, image science, and vision.

[7]  S. Hell,et al.  Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[8]  K. Fujita [Two-photon laser scanning fluorescence microscopy]. , 2007, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[9]  Jim Swoger,et al.  Tailoring the axial shape of the point spread function using the Toraldo concept. , 2002, Optics express.

[10]  T Wilson,et al.  Optimized pupil-plane filters for confocal microscope point-spread function engineering. , 2000, Optics letters.

[11]  Sherif S. Sherif,et al.  Pupil plane masks for super-resolution in high-numerical-aperture focusing , 2004 .

[12]  D. Grier A revolution in optical manipulation , 2003, Nature.

[13]  C J Sheppard Binary optics and confocal imaging. , 1999, Optics letters.

[14]  Satoshi Kawata,et al.  Finer features for functional microdevices , 2001, Nature.

[15]  J. Swoger,et al.  Single-lens theta microscopy: Resolution, efficiency and working distance , 1999 .

[16]  G Saavedra,et al.  Axial gain resolution in optical sectioning fluorescence microscopy by shaded-ring filters. , 2003, Optics express.

[17]  J. Miao,et al.  Atomic resolution three-dimensional electron diffraction microscopy. , 2002, Physical review letters.

[18]  Stefan W. Hell,et al.  Single sharp spot in fluorescence microscopy of two opposing lenses. , 2001 .

[19]  J. Pawley,et al.  Handbook of Biological Confocal Microscopy , 1990, Springer US.

[20]  Stefan Hell,et al.  Axial superresolution with ultrahigh aperture lenses. , 2002, Optics express.