Data di Pubblicazione:
2014
Abstract:
Solution-based single-molecule fluorescence spectroscopy
is a powerful experimental tool with applications in cell
biology, biochemistry, and biophysics. The basic feature of this
technique is to excite and collect light from a very small volume
and work in a low concentration regime resulting in rare burstlike
events corresponding to the transit of a single molecule. Detecting
photon bursts is a challenging task: the small number of
emitted photons in each burst calls for high detector sensitivity.
Bursts are very brief, requiring detectors with fast response time
and capable of sustaining high count rates. Finally, many bursts
need to be accumulated to achieve proper statistical accuracy, resulting
in long measurement time unless parallelization strategies
are implemented to speed up data acquisition. In this paper, we
will show that silicon single-photon avalanche diodes (SPADs) best
meet the needs of single-molecule detection. We will review the
key SPAD parameters and highlight the issues to be addressed in
their design, fabrication, and operation. After surveying the stateof-
the-art SPAD technologies, we will describe our recent progress
toward increasing the throughput of single-molecule fluorescence
spectroscopy in solution using parallel arrays of SPADs. The potential
of this approach is illustrated with single-molecule F¨orster
resonance energy transfer measurements.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Single-molecule; Fluorescence; FRET; FCS; single-photon avalanche diode; detector array.
Elenco autori:
Maccagnani, Piera
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