Quantitative imaging of protein-protein interactions by multiphoton fluorescence lifetime imaging microscopy using a streak camera

Fluorescence lifetime imaging microscopy (FLIM) using multiphoton excitation techniques is now finding an important place in quantitative imaging of protein-protein interactions and intracellular physiology. Recent developments in multiphoton FLIM methods are reviewed and a novel multiphoton FLIM sy...

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Veröffentlicht in:Journal of Biomedical Optics 2003-07, Vol.8 (3), p.362-367
Hauptverfasser: Krishnan, R. V, Masuda, A, Centonze, V. E, Herman, B
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container_title Journal of Biomedical Optics
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creator Krishnan, R. V
Masuda, A
Centonze, V. E
Herman, B
description Fluorescence lifetime imaging microscopy (FLIM) using multiphoton excitation techniques is now finding an important place in quantitative imaging of protein-protein interactions and intracellular physiology. Recent developments in multiphoton FLIM methods are reviewed and a novel multiphoton FLIM system using a streak camera is described. An example of a typical application of the system is provided in which the fluorescence resonance energy transfer between a donor-acceptor pair of fluorescent proteins within a cellular specimen is measured. ©
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subjects Animals
Bacterial Proteins
Caspase 2
Caspases - drug effects
Caspases - metabolism
Cells, Cultured
Cricetinae
Equipment Design
Equipment Failure Analysis
Feasibility Studies
fluorescence lifetime imaging microscopy
Fluorescence Resonance Energy Transfer - instrumentation
Fluorescence Resonance Energy Transfer - methods
Green Fluorescent Proteins
Kidney - cytology
Kidney - drug effects
Kidney - enzymology
Kidney - metabolism
Luminescent Proteins
Macromolecular Substances
Microscopy, Fluorescence, Multiphoton - instrumentation
Microscopy, Fluorescence, Multiphoton - methods
Microscopy, Video - instrumentation
Microscopy, Video - methods
Protein Binding
Recombinant Fusion Proteins - metabolism
tert-Butylhydroperoxide - pharmacology
Time Factors
title Quantitative imaging of protein-protein interactions by multiphoton fluorescence lifetime imaging microscopy using a streak camera
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