Abstract
The ability to observe the dynamic localization of a protein in living cells can provide critical insight to its mode of action and functional molecular interactions. To this purpose, green fluorescent protein (GFP) has served as a powerful tool to tag STAT proteins for microscopic visualization. Live cell imaging with STAT-GFP proteins has contributed to our understanding of signal transduction and the complexities of nuclear transport of STAT proteins. In this report we summarize recent approaches that use GFP-based techniques with live cell imaging to study the mechanisms of STAT nuclear import and export: photoactivation, fluorescence recovery after photobleaching (FRAP), and fluorescence loss in photobleaching (FLIP).
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Acknowledgments
This work was supported by grants from NIH (R56AI095268 and RO1CA122910) and a Carol M. Baldwin Breast Cancer Research Award to NCR.
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Cimica, V., Reich, N.C. (2013). Nuclear Trafficking of STAT Proteins Visualized by Live Cell Imaging. In: Nicholson, S., Nicola, N. (eds) JAK-STAT Signalling. Methods in Molecular Biology, vol 967. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-242-1_14
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DOI: https://doi.org/10.1007/978-1-62703-242-1_14
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