Localized light-induced protein dimerization in living cells using a photocaged dimerizer

Regulated protein localization is critical for many cellular processes. Several techniques have been developed for experimental control over protein localization, including chemically induced and light-induced dimerization, which both provide temporal control. Light-induced dimerization offers the d...

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Veröffentlicht in:Nature communications 2014-11, Vol.5 (1), p.5475-5475, Article 5475
Hauptverfasser: Ballister, Edward R., Aonbangkhen, Chanat, Mayo, Alyssa M., Lampson, Michael A., Chenoweth, David M.
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Sprache:eng
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Zusammenfassung:Regulated protein localization is critical for many cellular processes. Several techniques have been developed for experimental control over protein localization, including chemically induced and light-induced dimerization, which both provide temporal control. Light-induced dimerization offers the distinct advantage of spatial precision within subcellular length scales. A number of elegant systems have been reported that utilize natural light-sensitive proteins to induce dimerization via direct protein–protein binding interactions, but the application of these systems at cellular locations beyond the plasma membrane has been limited. Here we present a new technique to rapidly and reversibly control protein localization in living cells with subcellular spatial resolution using a cell-permeable, photoactivatable chemical inducer of dimerization. We demonstrate light-induced recruitment of a cytosolic protein to individual centromeres, kinetochores, mitochondria and centrosomes in human cells, indicating that our system is widely applicable to many cellular locations. Protein localization in cells can yield much information about the spatial arrangement of cellular processes and the participating groups. Here, the authors present a membrane-permeable and photoactive agent for localized protein dimerization in cells.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms6475