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000842811 1001_ $$0P:(DE-Juel1)131971$$aKatranidis, Alexandros$$b0$$eCorresponding author
000842811 245__ $$aCo-translational incorporation into proteins of a fluorophore suitable for smFRET studies
000842811 260__ $$aWashington, DC$$bACS$$c2018
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000842811 520__ $$aSingle-molecule FRET (smFRET) is a powerful tool to investigate conformational changes of biological molecules. In general, smFRET studies require protein samples that are site-specifically double-labeled with a pair of donor and acceptor fluorophores. The common approaches to produce such samples cannot be applied when studying the synthesis and folding of the polypeptide chain on the ribosome. The best strategy is to incorporate two fluorescent amino acids cotranslationally using cell-free protein synthesis systems. Here, we demonstrate the cotranslational site-specific incorporation into a model protein of Atto633, a dye with excellent photophysical properties, suitable for single molecule spectroscopy, together with a second dye using a combination of the sense cysteine and the nonsense amber codon. In this work we show that cotranslational incorporation of good fluorophores into proteins is a viable strategy to produce suitable samples for smFRET studies.
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000842811 7001_ $$0P:(DE-Juel1)166013$$aSadoine, Mayuri$$b1
000842811 7001_ $$0P:(DE-HGF)0$$aCerminara, M.$$b2
000842811 7001_ $$0P:(DE-HGF)0$$aGerrits, M.$$b3
000842811 7001_ $$0P:(DE-Juel1)131961$$aFitter, Jörg$$b4$$eCorresponding author
000842811 773__ $$0PERI:(DE-600)2644383-1$$a10.1021/acssynbio.7b00433$$gp. acssynbio.7b00433$$n2$$p405–411$$tACS synthetic biology$$v7$$x2161-5063$$y2018
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