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Construction and characterization of a frequency-domain fluorescence lifetime imaging microscopy system
Authors:Theodorus W. J. Gadella  Arie van Hoek  Antonie J. W. G. Visser
Affiliation:(1) MicroSpectroscopy Center (MSC) Wageningen, Department of Biochemistry, Wageningen Agricultural University, The Netherlands;(2) MSC Wageningen, Department of Molecular Physics, Wageningen Agricultural University, Wageningen, The Netherlands;(3) MSC Wageningen, Department of Molecular Biology, Wageningen Agricultural University, Dreijenlaan 3, NL-6703 HA Wageningen, The Netherlands
Abstract:The construction of a homodyne frequency domain fluorescence lifetime imaging microscope is described. The system consists of (i) an intensity-modulated laser excitation source, (ii) an epifluorescence microscope, (iii) a gain-modulated microchannel plate (MCP) image intensifier, and (iv) a slow-scan CCD camera. The phase and modulation homogeneity of the MCP image intensifier were determined at frequencies of 40, 100, 160, and 240 MHz. The detected modulation depths were 65, 52, 32, and 23%, respectively, and were highly homogeneously distributed. The phasedistribution image revealed iris effects at frequencies of 160 and 240 MHz but was homogeneous at lower frequencies. Lifetime imaging of a solution of the fluorescent flavoprotein lipoamide dehydrogenase demonstrated (i) the accuracy of the determined lifetimes (< 60 ps), (ii) the time resolution of the instrument (< 50 ps), and (iii) the average precision for single pixel fluorescence lifetimes (50 ps is feasible). The imaging of tiny fluorescent microspheres revealed that even in a volume of 0.3 x 10-15 L, the standard error in the lifetimes can be as low as 79 ps. The spatial resolution of the instrument is estimated to be < 400 nm in the object plane at a 100 x magnification.
Keywords:Time-resolved fluorescence  image intensifier  modulation  image processing
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