Title of article
Fluorescence microscopy of single autofluorescent proteins for cellular biology
Author/Authors
Cognet، نويسنده , , Laurent and Coussen، نويسنده , , Françoise and Choquet، نويسنده , , Daniel and Lounis، نويسنده , , Brahim، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2002
Pages
12
From page
645
To page
656
Abstract
In this paper we review the applicability of autofluorescent proteins for single-molecule imaging in biology. The photophysical characteristics of several mutants of the Green Fluorescent Protein (GFP) and those of DsRed are compared and critically discussed for their use in cellular biology. The alternative use of two-photon excitation at the single-molecule level or Fluorescence Correlation Spectroscopy is envisaged for the study of individual autofluorescent proteins. Single-molecule experiments performed in live cells using eGFP and preferably eYFP fusion proteins are reviewed. Finally, the first use at the single-molecule level of citrine, a more photostable variant of the eYFP is reported when fused to a receptor for neurotransmitter in live cells. To cite this article: L. Cognet et al., C. R. Physique 3 (2002) 645–656.
Keywords
GFP , GFP , fluorescence microscopy , two-photon excitation , fluorescence correlation spectroscopy , DsRed , DsRed , single-molecule , détection de molécules uniques , microscopie de fluorescence , excitation à deux photons , spectroscopie par corrélation de fluorescence
Journal title
Comptes Rendus Physique
Serial Year
2002
Journal title
Comptes Rendus Physique
Record number
2283073
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