Literature DB >> 21034069

High-performance time-resolved fluorescence by direct waveform recording.

Joseph M Muretta1, Alexander Kyrychenko, Alexey S Ladokhin, David J Kast, Gregory D Gillispie, David D Thomas.   

Abstract

We describe a high-performance time-resolved fluorescence (HPTRF) spectrometer that dramatically increases the rate at which precise and accurate subnanosecond-resolved fluorescence emission waveforms can be acquired in response to pulsed excitation. The key features of this instrument are an intense (1 μJ/pulse), high-repetition rate (10 kHz), and short (1 ns full width at half maximum) laser excitation source and a transient digitizer (0.125 ns per time point) that records a complete and accurate fluorescence decay curve for every laser pulse. For a typical fluorescent sample containing a few nanomoles of dye, a waveform with a signal/noise of about 100 can be acquired in response to a single laser pulse every 0.1 ms, at least 10(5) times faster than the conventional method of time-correlated single photon counting, with equal accuracy and precision in lifetime determination for lifetimes as short as 100 ps. Using standard single-lifetime samples, the detected signals are extremely reproducible, with waveform precision and linearity to within 1% error for single-pulse experiments. Waveforms acquired in 0.1 s (1000 pulses) with the HPTRF instrument were of sufficient precision to analyze two samples having different lifetimes, resolving minor components with high accuracy with respect to both lifetime and mole fraction. The instrument makes possible a new class of high-throughput time-resolved fluorescence experiments that should be especially powerful for biological applications, including transient kinetics, multidimensional fluorescence, and microplate formats.

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Year:  2010        PMID: 21034069      PMCID: PMC2980540          DOI: 10.1063/1.3480647

Source DB:  PubMed          Journal:  Rev Sci Instrum        ISSN: 0034-6748            Impact factor:   1.523


  8 in total

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5.  Structural dynamics of the myosin relay helix by time-resolved EPR and FRET.

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6.  The use of standards in the analysis of fluorescence decay data.

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  8 in total
  32 in total

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Authors:  Simon J Gruber; Suzanne Haydon; David D Thomas
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9.  A Novel Fluorescence Resonance Energy Transfer-Based Screen in High-Throughput Format To Identify Inhibitors of Malarial and Human Glucose Transporters.

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10.  Discovery of enzyme modulators via high-throughput time-resolved FRET in living cells.

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