Highly versatile confocal microscopy system based on a tunable femtosecond Er:fiber source

The performance of a confocal microscopy setup based on a single femtosecond fiber system is explored over a broad range of pump wavelengths for both linear and nonlinear imaging techniques. First, the benefits of a laser source in linear fluorescence excitation that is continuously tunable over most of the visible spectrum are demonstrated. The influences of subpicosecond pulse durations on the bleaching behavior of typical fluorophores are discussed. We then utilize the tunable near-infrared output of the femtosecond system in connection with a specially designed prism compressor for dispersion control. Pulses as short as 33 fs are measured in the confocal region. As a consequence, 2 mW of average power are sufficient for two-photon microscopy in an organotypic sample from the mouse brain. This result shows great prospect for deep-tissue imaging in the optimum transparency window around 1100 nm. In a third experiment, we prove that our compact setup is powerful enough to exploit even higher-order nonlinearities such as three-photon absorption that we use to induce spatially localized photodamage in DNA.

[1]  Rongqing Hui,et al.  Two-photon microscopy with wavelength switchable fiber laser excitation. , 2006, Optics express.

[2]  K R Wilson,et al.  Third-harmonic generation microscopy by use of a compact, femtosecond fiber laser source. , 1999, Applied optics.

[3]  W. Denk,et al.  Deep tissue two-photon microscopy , 2005, Nature Methods.

[4]  Thomas Feurer,et al.  Characterization and optimization of a laser-scanning microscope in the femtosecond regime , 1998 .

[5]  Z. Bor,et al.  Distortion of femtosecond laser pulses in lenses and lens systems. , 1988 .

[6]  H. Gerritsen,et al.  Short-wavelength two-photon excitation fluorescence microscopy of tryptophan with a photonic crystal fiber based light source. , 2005, Optics express.

[7]  D. Johnston,et al.  A modified Sindbis vector for prolonged gene expression in neurons. , 2003, Journal of neurophysiology.

[8]  Christian Eggeling,et al.  Major signal increase in fluorescence microscopy through dark-state relaxation , 2007, Nature Methods.

[9]  G McConnell,et al.  Nonlinear optical microscopy at wavelengths exceeding 1.4 µm using a synchronously pumped femtosecond-pulsed optical parametric oscillator , 2007, Physics in medicine and biology.

[10]  Chi-Kuang Sun,et al.  In vivo optical biopsy of hamster oral cavity with epi-third-harmonic-generation microscopy. , 2006, Optics express.

[11]  Yaron Silberberg,et al.  Nonlinear scanning laser microscopy by third harmonic generation , 1997 .

[12]  S. Chu,et al.  Nonlinear bio‐photonic crystal effects revealed with multimodal nonlinear microscopy , 2002, Journal of microscopy.

[13]  Chi‐Kuang Sun,et al.  Multiphoton confocal microscopy using a femtosecond Cr:Forsterite laser , 2006 .

[14]  A. Bürkle Physiology and pathophysiology of poly(ADP‐ribosyl)ation * , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.

[15]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[16]  C. Limoli,et al.  A new method for introducing double-strand breaks into cellular DNA. , 1993, Radiation research.

[17]  Andrew G. Glen,et al.  APPL , 2001 .

[18]  Alfred Leitenstorfer,et al.  Widely tunable sub-30-fs pulses from a compact erbium-doped fiber source. , 2004, Optics letters.

[19]  A. Leitenstorfer,et al.  Highly efficient second, third and fourth harmonic generation from a two- branch femtosecond erbium fiber source. , 2006, Optics express.

[20]  W. Webb,et al.  Nonlinear magic: multiphoton microscopy in the biosciences , 2003, Nature Biotechnology.

[21]  Eric Mottay,et al.  Novel diode‐pumped infrared tunable laser system for multi‐photon microscopy , 2004, Microscopy research and technique.

[22]  H Goncalves,et al.  Scanning , 2004, IEEE Trans. Autom. Control..

[23]  R. Anderson,et al.  The optics of human skin. , 1981, The Journal of investigative dermatology.

[24]  D. Shcherbo,et al.  Bright far-red fluorescent protein for whole-body imaging , 2007, Nature Methods.

[25]  C. Dunsby,et al.  An electronically tunable ultrafast laser source applied to fluorescence imaging and fluorescence lifetime imaging microscopy , 2004, (CLEO). Conference on Lasers and Electro-Optics, 2005..

[26]  Ingo Rimke,et al.  Infrared multiphoton microscopy beyond 1 micron: system design and biomedical applications , 2007, SPIE BiOS.

[27]  R. Meldrum,et al.  Nanoscale spatial induction of ultraviolet photoproducts in cellular DNA by three‐photon near‐infrared absorption , 2003, EMBO reports.

[28]  Harald Giessen,et al.  Diode-pumped, ultrafast, multi-octave supercontinuum source at repetition rates between 500 kHz and 20 MHz using Yb:glass lasers and tapered fibers. , 2005, Optics express.

[29]  Miss A.O. Penney (b) , 1974, The New Yale Book of Quotations.

[30]  Alfred Leitenstorfer,et al.  Amplified femtosecond pulses from an Er:fiber system: Nonlinear pulse shortening and selfreferencing detection of the carrier-envelope phase evolution. , 2003, Optics express.

[31]  D. Träutlein,et al.  Multimilliwatt ultrashort pulses continuously tunable in the visible from a compact fiber source. , 2006, Optics letters.

[32]  Gail McConnell,et al.  Confocal laser scanning fluorescence microscopy with a visible continuum source. , 2004, Optics express.

[33]  Andreas Volkmer,et al.  Molecular photobleaching kinetics of Rhodamine 6G by one- and two-photon induced confocal fluorescence microscopy. , 2005, Chemphyschem : a European journal of chemical physics and physical chemistry.

[34]  R. Tsien,et al.  Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein , 2004, Nature Biotechnology.

[35]  G J Brakenhoff,et al.  Measurement of femtosecond pulses in the focal point of a high-numerical-aperture lens by two-photon absorption. , 1995, Optics letters.

[36]  J. Käs,et al.  Excitation beyond the monochromatic laser limit: simultaneous 3-D confocal and multiphoton microscopy with a tapered fiber as white-light laser source. , 2005, Journal of biomedical optics.