Solution-based single-molecule fluorescence spectroscopy is a powerful new experimental approach with applications in all fields of natural sciences. The basic concept of this technique is to excite and collect light from a very small volume (typically femtoliter) and work in a concentration regime resulting in rare burst-like events corresponding to the transit of a single-molecule. Those events are accumulated over time to achieve proper statistical accuracy. Therefore the advantage of extreme sensitivity is somewhat counterbalanced by a very long acquisition time. One way to speed up data acquisition is parallelization. Here we will discuss a general approach to address this issue, using a multispot excitation and detection geometry that can accommodate different types of novel highly-parallel detector arrays. We will illustrate the potential of this approach with fluorescence correlation spectroscopy (FCS) and single-molecule fluorescence measurements obtained with different novel multipixel single-photon counting detectors.

High-throughput single-molecule fluorescence spectroscopyusing parallel detection

GUERRIERI, FABRIZIO;RECH, IVAN;RESNATI, DANIELE;MARANGONI, STEFANO;GULINATTI, ANGELO;GHIONI, MASSIMO ANTONIO;TISA, SIMONE;ZAPPA, FRANCO;COVA, SERGIO;
2010-01-01

Abstract

Solution-based single-molecule fluorescence spectroscopy is a powerful new experimental approach with applications in all fields of natural sciences. The basic concept of this technique is to excite and collect light from a very small volume (typically femtoliter) and work in a concentration regime resulting in rare burst-like events corresponding to the transit of a single-molecule. Those events are accumulated over time to achieve proper statistical accuracy. Therefore the advantage of extreme sensitivity is somewhat counterbalanced by a very long acquisition time. One way to speed up data acquisition is parallelization. Here we will discuss a general approach to address this issue, using a multispot excitation and detection geometry that can accommodate different types of novel highly-parallel detector arrays. We will illustrate the potential of this approach with fluorescence correlation spectroscopy (FCS) and single-molecule fluorescence measurements obtained with different novel multipixel single-photon counting detectors.
2010
Quantum Sensing and Nanophotonic Devices VII
9780819480040
sezele; single-molecule; fluorescence; spectroscopy; photon-counting; FRET; FCS; SPAD; array
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/570181
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