We present the development and first application of a novel dual-color total internal reflection (TIR) fluorescence system for single-molecule coincidence analysis and fluorescence cross-correlation spectroscopy (FCCS). As a performance analysis, we measured a synthetic DNA-binding assay, demonstrating this dual-color TIR-FCCS approach to be a suitable method for measuring coincidence assays such as biochemical binding, fusion, or signal transduction at solid/liquid interfaces. Due to the very high numerical aperture of the epi-illumination configuration, our setup provides a very high fluorescence collection efficiency resulting in a two- to three-fold increase in molecular brightness compared to conventional confocal FCCS. Further improvements have been achieved through global analysis of the spectroscopic data. © 2006 Society of Photo-Optical Instrumentation Engineers.
CITATION STYLE
Leutenegger, M., Blom, H., Widengren, J., Eggeling, C., Gösch, M., Leitgeb, R. A., & Lasser, T. (2006). Dual-color total internal reflection fluorescence cross-correlation spectroscopy. Journal of Biomedical Optics, 11(4), 040502. https://doi.org/10.1117/1.2221714
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