Contact-mediated quenching for RNA imaging in bacteria with a fluorophore-binding aptamer

Bind and shine: Sulforhodamine B was converted into a very efficient fluorescence turn-on probe exclusively by contact quenching. The fluorescence of the probe increases more than 100-fold upon binding to a sulforhodamine-binding RNA aptamer (SRB-2). The probe and the SRB-2 aptamer were used to moni...

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Bibliographic Details
Main Authors: Sünbül, Murat (Author) , Jäschke, Andres (Author)
Format: Article (Journal)
Language:English
Published: October 16, 2013
In: Angewandte Chemie. International edition
Year: 2013, Volume: 52, Issue: 50, Pages: 13401-13404
ISSN:1521-3773
DOI:10.1002/anie.201306622
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/anie.201306622
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201306622
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Author Notes:Murat Sunbul and Andres Jäschke
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Summary:Bind and shine: Sulforhodamine B was converted into a very efficient fluorescence turn-on probe exclusively by contact quenching. The fluorescence of the probe increases more than 100-fold upon binding to a sulforhodamine-binding RNA aptamer (SRB-2). The probe and the SRB-2 aptamer were used to monitor transcriptions in real-time and to image RNA in live bacteria.
Item Description:Gesehen am 27.01.2022
Physical Description:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.201306622