Fluorescence resonance energy transfer (FRET) measurement by gradual acceptor photobleaching
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E. V. van Munster | T. Gadella | M. Adjobo-Hermans | E B Van Munster | G J Kremers | M J W Adjobo-Hermans | T W J Gadella | G. Kremers
[1] Gaudenz Danuser,et al. FRET or no FRET: a quantitative comparison. , 2003, Biophysical journal.
[2] R. Young,et al. Quantitation of fluorescence energy transfer between cell surface proteins via fluorescence donor photobleaching kinetics. , 1994, Biophysical journal.
[3] P. Bastiaens,et al. Three dimensional image restoration in fluorescence lifetime imaging microscopy , 1999, Journal of microscopy.
[4] Kees Jalink,et al. Correcting confocal acquisition to optimize imaging of fluorescence resonance energy transfer by sensitized emission. , 2004, Biophysical journal.
[5] P. Verveer,et al. Red-edge anisotropy microscopy enables dynamic imaging of homo-FRET between green fluorescent proteins in cells. , 2004, Journal of structural biology.
[6] E. Nice,et al. Dual-channel photobleaching FRET microscopy for improved resolution of protein association states in living cells , 2005, European Biophysics Journal.
[7] T M Jovin,et al. Distribution of type I Fc epsilon-receptors on the surface of mast cells probed by fluorescence resonance energy transfer. , 1993, Biophysical journal.
[8] G. Patterson,et al. Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy. , 1997, Biophysical journal.
[9] I. T. Young,et al. Influence of fluorochrome labeling density on the photobleaching kinetics of fluorescein in microscopy. , 1997, Cytometry.
[10] John A. Nelder,et al. A Simplex Method for Function Minimization , 1965, Comput. J..
[11] T M Jovin,et al. FRET microscopy demonstrates molecular association of non‐specific lipid transfer protein (nsL‐TP) with fatty acid oxidation enzymes in peroxisomes , 1998, The EMBO journal.
[12] Y. Liu,et al. Reliable and global measurement of fluorescence resonance energy transfer using fluorescence microscopes. , 2001, Biophysical journal.
[13] R. Tsien,et al. green fluorescent protein , 2020, Catalysis from A to Z.
[14] I. T. Young,et al. Photobleaching kinetics of fluorescein in quantitative fluorescence microscopy. , 1995, Biophysical journal.
[15] R. Tsien,et al. Fluorescent indicators for Ca2+based on green fluorescent proteins and calmodulin , 1997, Nature.
[16] A Miyawaki,et al. Dynamic and quantitative Ca2+ measurements using improved cameleons. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[17] Stephen J. Lockett,et al. Intensity-based energy transfer measurements in digital imaging microscopy , 1998, European Biophysics Journal.
[18] E. V. van Munster,et al. φFLIM: a new method to avoid aliasing in frequency‐domain fluorescence lifetime imaging microscopy , 2004, Journal of microscopy.
[19] V. Subramaniam,et al. Photophysics of green and red fluorescent proteins: implications for quantitative microscopy. , 2003, Methods in enzymology.
[20] J. Swanson,et al. Fluorescence resonance energy transfer-based stoichiometry in living cells. , 2002, Biophysical journal.
[21] .. C.N.Fokunang,et al. Advancement in Genetic Modification Technologies Towards Disease Resistance and Food Crop Production , 2004 .
[22] Z. Derewenda,et al. Overcoming expression and purification problems of RhoGDI using a family of "parallel" expression vectors. , 1999, Protein Expression and Purification.
[23] Mark A Rizzo,et al. An improved cyan fluorescent protein variant useful for FRET , 2004, Nature Biotechnology.
[24] Thomas M. Jovin,et al. FRET Microscopy: Digital Imaging of Fluorescence Resonance Energy Transfer. Application in Cell Biology , 1989 .
[25] E. V. van Munster,et al. Fluorescence lifetime imaging microscopy (FLIM). , 2005, Advances in biochemical engineering/biotechnology.
[26] T M Jovin,et al. Luminescence digital imaging microscopy. , 1989, Annual review of biophysics and biophysical chemistry.
[27] A. Miyawaki,et al. Spatio-temporal images of growth-factor-induced activation of Ras and Rap1 , 2001, Nature.
[28] R. Tsien,et al. On/off blinking and switching behaviour of single molecules of green fluorescent protein , 1997, Nature.
[29] P J Verveer,et al. Evaluation of global analysis algorithms for single frequency fluorescence lifetime imaging microscopy data , 2003, Journal of microscopy.
[30] V. Mekler,et al. Fluorescence energy transfer-sensitized photobleaching of a fluorescent label as a tool to study donor-acceptor distance distributions and dynamics in protein assemblies: studies of a complex of biotinylated IgM with streptavidin and aggregates of concanavalin A. , 1997, Journal of photochemistry and photobiology. B, Biology.
[31] Robert M. Clegg,et al. Fluorescence lifetime imaging microscopy (FLIM): Spatial resolution of microstructures on the nanosecond time scale , 1993 .
[32] Konstantin A Lukyanov,et al. Photoswitchable cyan fluorescent protein for protein tracking , 2004, Nature Biotechnology.
[33] Y. Umezawa,et al. Fluorescent indicators for imaging protein phosphorylation in single living cells , 2002, Nature Biotechnology.
[34] V. Mekler. A PHOTOCHEMICAL TECHNIQUE TO ENHANCE SENSITIVITY OF DETECTION OF FLUORESCENCE RESONANCE ENERGY TRANSFER , 1994 .
[35] A. Kenworthy,et al. Imaging protein-protein interactions using fluorescence resonance energy transfer microscopy. , 2001, Methods.
[36] R. Pepperkok,et al. Spectral imaging and its applications in live cell microscopy , 2003, FEBS letters.
[37] J. Post,et al. Imaging molecular interactions in cells by dynamic and static fluorescence anisotropy (rFLIM and emFRET). , 2003, Biochemical Society transactions.
[38] E. V. van Munster,et al. Suppression of photobleaching‐induced artifacts in frequency‐domain FLIM by permutation of the recording order , 2004, Cytometry. Part A : the journal of the International Society for Analytical Cytology.
[39] Th. Förster. Zwischenmolekulare Energiewanderung und Fluoreszenz , 1948 .
[40] Christian Blum,et al. Room temperature spectrally resolved single-molecule spectroscopy reveals new spectral forms and photophysical versatility of aequorea green fluorescent protein variants. , 2004, Biophysical journal.
[41] Squire,et al. Multiple frequency fluorescence lifetime imaging microscopy , 2000, Journal of microscopy.
[42] T. Jovin,et al. FRET imaging , 2003, Nature Biotechnology.
[43] Marcus J. Grote,et al. The Collection, Processing, and Display of Digital Three-Dimensional Images of Biological Specimens , 1995 .
[44] William H. Press,et al. Numerical recipes in C , 2002 .
[45] R. Tsien,et al. Fluorescence resonance energy transfer analysis of cell surface receptor interactions and signaling using spectral variants of the green fluorescent protein. , 2001, Cytometry.
[46] B. Herman,et al. Quantitative fluorescence resonance energy transfer measurements using fluorescence microscopy. , 1998, Biophysical journal.
[47] R. Tsien,et al. Ligand-dependent interactions of coactivators steroid receptor coactivator-1 and peroxisome proliferator-activated receptor binding protein with nuclear hormone receptors can be imaged in live cells and are required for transcription. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[48] Takeharu Nagai,et al. Crystal Structure of Venus, a Yellow Fluorescent Protein with Improved Maturation and Reduced Environmental Sensitivity* , 2002, The Journal of Biological Chemistry.
[49] D Zicha,et al. Quantitative fluorescence resonance energy transfer (FRET) measurement with acceptor photobleaching and spectral unmixing , 2004, Journal of microscopy.
[50] Thomas M. Jovin,et al. Fluorescence Resonance Energy Transfer Microscopy , 1998 .