Visible-wavelength two-photon excitation microscopy for fluorescent protein imaging
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Satoshi Kawata | Takeharu Nagai | Yasuo Yonemaru | Masahito Yamanaka | Katsumasa Fujita | Yoshiyuki Arai | Nicholas I Smith | Kenta Saito | Kentaro Mochizuki | Kumiko Uegaki | S. Kawata | T. Nagai | Y. Arai | Kenta Mochizuki | K. Fujita | N. Smith | M. Yamanaka | Kenta Saito | Y. Yonemaru | K. Uegaki | K. Mochizuki
[1] P. Schwille,et al. Simultaneous two-photon excitation of distinct labels for dual-color fluorescence crosscorrelation analysis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[2] Liisa M. Hirvonen,et al. DEEP-UV CONFOCAL FLUORESCENCE IMAGING AND SUPER-RESOLUTION OPTICAL MICROSCOPY OF BIOLOGICAL SAMPLES , 2012 .
[3] Fu-Jen Kao,et al. The use of optical parametric oscillator for harmonic generation and two‐photon UV fluorescence microscopy , 2004, Microscopy research and technique.
[4] J. Lakowicz. Principles of fluorescence spectroscopy , 1983 .
[5] Arie van Hoek,et al. Direct observation of resonance tryptophan-to-chromophore energy transfer in visible fluorescent proteins. , 2005, Biophysical chemistry.
[6] Takeharu Nagai,et al. An ultramarine fluorescent protein with increased photostability and pH insensitivity , 2009, Nature Methods.
[7] M. Drobizhev,et al. Resonance enhancement of two-photon absorption in fluorescent proteins. , 2007, The journal of physical chemistry. B.
[8] G. J. Brakenhoff,et al. 3‐D image formation in high‐aperture fluorescence confocal microscopy: a numerical analysis , 1990 .
[9] Michael W. Davidson,et al. The fluorescent protein palette: tools for cellular imaging. , 2009, Chemical Society reviews.
[10] S. Hell,et al. Aberrations in confocal fluorescence microscopy induced by mismatches in refractive index , 1993 .
[11] R. Pepperkok,et al. Spectral imaging and linear un‐mixing enables improved FRET efficiency with a novel GFP2–YFP FRET pair , 2002, FEBS letters.
[12] W. Webb,et al. Nonlinear magic: multiphoton microscopy in the biosciences , 2003, Nature Biotechnology.
[13] G. McConnell,et al. Increased signals from short-wavelength-excited fluorescent molecules using sub-Ti:Sapphire wavelengths , 2012, Journal of microscopy.
[14] Robert E Campbell,et al. Directed evolution of a monomeric, bright and photostable version of Clavularia cyan fluorescent protein: structural characterization and applications in fluorescence imaging. , 2006, The Biochemical journal.
[15] James B. Pawley,et al. Confocal and two‐photon microscopy: Foundations, applications and advances , 2002 .
[16] Charles P. Lin,et al. Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy , 2012, Biomedical optics express.
[17] R. Tsien,et al. Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein , 2004, Nature Biotechnology.
[18] Aleksander Rebane,et al. Simultaneous multiple-excitation multiphoton microscopy yields increased imaging sensitivity and specificity , 2011, BMC biotechnology.
[19] M. Chalfie. GREEN FLUORESCENT PROTEIN , 1995, Photochemistry and photobiology.
[20] O. Nakamura,et al. Three-dimensional imaging characteristics of laser scan fluorescence microscopy--Two-photon excitation vs.single-photon excitation , 1993 .
[21] Tony Wilson,et al. Principles of Three-Dimensional Imaging in Confocal Microscopes. , 1999 .
[22] M. Drobizhev,et al. Two-photon absorption properties of fluorescent proteins , 2011, Nature Methods.
[23] M. Gu,et al. Principles Of Three-Dimensional Imaging In Confocal Microscopes , 1996 .
[24] S. Lukyanov,et al. Fluorescent proteins from nonbioluminescent Anthozoa species , 1999, Nature Biotechnology.
[25] Colin J. R. Sheppard,et al. Image formation in two-photon fluorescence microscopy , 1990 .
[26] P. So,et al. Two‐photon excited lifetime imaging of autofluorescence in cells during UV A and NIR photostress , 1996, Journal of microscopy.
[27] W. Webb,et al. Measuring Serotonin Distribution in Live Cells with Three-Photon Excitation , 1997, Science.
[28] Shou-Ping Jiang,et al. Two-photon excitation of proteins , 1984 .
[29] W. Denk,et al. Deep tissue two-photon microscopy , 2005, Nature Methods.
[30] N. Omenetto,et al. Fluorescence behavior of 7-hydroxycoumarine excited by one-photon and two-photon absorption by means of a tunable dye laser , 1978 .
[31] O Nakamura. A two-photon scanning fluorescence microscope with deep UV excitation and near UV detection , 1995 .
[32] W. Denk,et al. Two-photon laser scanning fluorescence microscopy. , 1990, Science.
[33] S. Hell,et al. Multifocal multiphoton microscopy. , 1998, Optics letters.
[34] Atsushi Miyawaki,et al. Fluorescence imaging using a fluorescent protein with a large Stokes shift. , 2008, Methods.
[35] Guillaume Labroille,et al. Multicolor two-photon tissue imaging by wavelength mixing , 2012, Nature Methods.
[36] Stefan Engelhardt,et al. Analysis of receptor oligomerization by FRAP microscopy , 2009, Nature Methods.
[37] Greg Norris,et al. A promising new wavelength region for three-photon fluorescence microscopy of live cells , 2012, Journal of microscopy.
[38] Robert R. Alfano,et al. Noninvasive two-photon-excitation imaging of tryptophan distribution in highly scattering biological tissues , 1998 .
[39] T Wilson,et al. Full spectrum filterless fluorescence microscopy , 2010, Journal of microscopy.
[40] Satoshi Kawata,et al. High-resolution confocal microscopy by saturated excitation of fluorescence. , 2007, Physical review letters.
[41] W. Webb,et al. Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[42] Takeharu Nagai,et al. Shift anticipated in DNA microarray market , 2002, Nature Biotechnology.
[43] S. Hell,et al. Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy. , 1994, Optics letters.
[44] Robert E Campbell,et al. Exploration of new chromophore structures leads to the identification of improved blue fluorescent proteins. , 2007, Biochemistry.
[45] Satoshi Kawata,et al. Confocal multipoint multiphoton excitation microscope with microlens and pinhole arrays , 2000 .
[46] Mikhail Drobizhev,et al. A new approach to dual-color two-photon microscopy with fluorescent proteins , 2010, BMC biotechnology.
[47] Shigeo Hayashi,et al. Improving spinning disk confocal microscopy by preventing pinhole cross-talk for intravital imaging , 2013, Proceedings of the National Academy of Sciences.
[48] K. Gericke,et al. Two-Color Two-Photon Fluorescence Laser Scanning Microscopy , 2009, Journal of Fluorescence.
[49] Atsushi Miyawaki,et al. A fluorescent variant of a protein from the stony coral Montipora facilitates dual-color single-laser fluorescence cross-correlation spectroscopy , 2006, Nature Biotechnology.
[50] Takeharu Nagai,et al. Direct measurement of protein dynamics inside cells using a rationally designed photoconvertible protein , 2008, Nature Methods.
[51] S. Maiti,et al. Live cell ultraviolet microscopy: A comparison between two‐ and three‐photon excitation , 2004, Microscopy research and technique.
[52] W. Webb,et al. Multiphoton fluorescence excitation: new spectral windows for biological nonlinear microscopy. , 1996, Proceedings of the National Academy of Sciences of the United States of America.