| Literature DB >> 27468728 |
Annette Buntz1, Sarah Wallrodt2, Eva Gwosch3, Michael Schmalz4, Sascha Beneke3, Elisa Ferrando-May3, Andreas Marx5, Andreas Zumbusch6.
Abstract
Poly(ADP-ribos)ylation (PARylation) is an important posttranslational protein modification, and is involved in major cellular processes such as gene regulation and DNA repair. Its dysregulation has been linked to several diseases, including cancer. Despite its importance, methods to observe PARylation dynamics within cells are rare. By following a chemical biology approach, we developed a fluorescent NAD(+) analogue that proved to be a competitive building block for protein PARylation in vitro and in cells. This allowed us to directly monitor the turnover of PAR in living cells at DNA damage sites after near-infrared (NIR) microirradiation. Additionally, covalent and noncovalent interactions of selected target proteins with PAR chains were visualized in cells by using FLIM-FRET microscopy. Our results open up new opportunities for the study of protein PARylation in real time and in live cells, and will thus contribute to a better understanding of its significance in a cellular context.Entities:
Keywords: DNA repair; FRET; NAD+; poly(ADP-ribose); posttranslational modifications
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Year: 2016 PMID: 27468728 DOI: 10.1002/anie.201605282
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336