One Assay for All: Exploring Small Molecule Phosphorylation Using Amylose–Polyiodide Complexes

We present a generic method for screening small molecule kinases for their acceptor specificity. The release of the reaction byproduct adenosine diphosphate (ADP) triggers a concentration-dependent formation of amylose from sucrose, by using the combined enzymatic action of sucrose synthase and glyc...

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Veröffentlicht in:Analytical chemistry (Washington) 2015-10, Vol.87 (19), p.9546-9550
Hauptverfasser: Duan, Xu C., Chen, Huan, Liu, Fang F., Conway, Louis, Wei, Shuang, Cai, Zhi P., Liu, Li, Voglmeir, Josef
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Sprache:eng
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Zusammenfassung:We present a generic method for screening small molecule kinases for their acceptor specificity. The release of the reaction byproduct adenosine diphosphate (ADP) triggers a concentration-dependent formation of amylose from sucrose, by using the combined enzymatic action of sucrose synthase and glycogen synthase. Kinase activities could be quantified photometrically after the formation of a dark-blue amylose–polyiodide complex. We demonstrate that this method can be used to profile both known and novel nucleotide- and sugar-kinases for their substrate specificity. Using a facile and widely available methodology, the amylose–polyiodide small-molecule kinase assay presented herein has the potential to perform substrate screenings of small molecule kinases in a high-throughput manner.
ISSN:0003-2700
1520-6882
DOI:10.1021/acs.analchem.5b02247