1 May 2008 Robust single-molecule approach for counting autofluorescent proteins
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Using single-molecule microscopy, we present a method to quantify the number of single autofluorescent proteins when they cannot be optically resolved. This method relies on the measurement of the total intensity emitted by each aggregate until it photobleaches. This strategy overcomes the inherent problem of blinking of green fluorescent proteins. In the case of small protein aggregates, our method permits us to describe the mean composition with a precision of one protein. For aggregates containing a large number of proteins, it gives access to the average number of proteins gathered and a signature of the inhomogeneity of the aggregates' population. We applied this methodology to the quantification of small purified citrine multimers.
© (2008) Society of Photo-Optical Instrumentation Engineers (SPIE)
Laurent Cognet, Laurent Cognet, Catherine Tardin, Catherine Tardin, Marie-Laure Martin Negrier, Marie-Laure Martin Negrier, Christelle Breillat, Christelle Breillat, Francoise Coussen, Francoise Coussen, Daniel Choquet, Daniel Choquet, Brahim Lounis, Brahim Lounis, } "Robust single-molecule approach for counting autofluorescent proteins," Journal of Biomedical Optics 13(3), 031216 (1 May 2008). https://doi.org/10.1117/1.2940600 . Submission:

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