Quantifying the influence of yellow fluorescent protein photoconversion on acceptor photobleaching–based fluorescence resonance energy transfer measurements
Arne Seitz, Stefan Terjung, Timo Zimmermann, Rainer Pepperkok
Abstract
Open-access reader
Arne Seitz, Stefan Terjung, Timo Zimmermann, Rainer Pepperkok
Abstract
Open-access reader
Fluorescence resonance energy transfer (FRET) efficiency measurements based on acceptor photobleaching of yellow fluorescent protein (YFP) are affected by the fact that bleaching of YFP produces a fluorescent species that is detectable in cyan fluorescent protein (CFP) image channels. The presented quantitative measurement of this conversion makes it possible to correct the obtained FRET signal to increase the accuracy of intensity based CFP/YFP FRET measurements. The described method can additionally be used to compare samples with very different fluorescence levels.
OpenAlex reports 9 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Fluorescence resonance energy transfer (FRET) efficiency measurements based on acceptor photobleaching of yellow fluorescent protein (YFP) are affected by the fact that bleaching of YFP produces a fluorescent species that is detectable in cyan fluorescent protein (CFP) image channels. The presented quantitative measurement of this conversion makes it possible to correct the obtained FRET signal to increase the accuracy of intensity based CFP/YFP FRET measurements. The described method can additionally be used to compare samples with very different fluorescence levels.
Key concepts: Förster resonance energy transfer, Photobleaching, Fluorescence, Yellow fluorescent protein, Acceptor, Green fluorescent protein, Fluorescence recovery after photobleaching, Fluorescent protein