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Semi-Automated High-Throughput Substrate Screening Assay for Nucleoside Kinases.
Hellendahl, Katja F; Fehlau, Maryke; Hans, Sebastian; Neubauer, Peter; Kurreck, Anke.
  • Hellendahl KF; Chair of Bioprocess Engineering, Faculty III Process Sciences, Institute of Biotechnology, Technische Universität Berlin, Ackerstraße 76, 13355 Berlin, Germany.
  • Fehlau M; Chair of Bioprocess Engineering, Faculty III Process Sciences, Institute of Biotechnology, Technische Universität Berlin, Ackerstraße 76, 13355 Berlin, Germany.
  • Hans S; BioNukleo GmbH, Ackerstraße 76, 13355 Berlin, Germany.
  • Neubauer P; Chair of Bioprocess Engineering, Faculty III Process Sciences, Institute of Biotechnology, Technische Universität Berlin, Ackerstraße 76, 13355 Berlin, Germany.
  • Kurreck A; Chair of Bioprocess Engineering, Faculty III Process Sciences, Institute of Biotechnology, Technische Universität Berlin, Ackerstraße 76, 13355 Berlin, Germany.
Int J Mol Sci ; 22(21)2021 Oct 26.
Article in English | MEDLINE | ID: covidwho-1512374
ABSTRACT
Nucleoside kinases (NKs) are key enzymes involved in the in vivo phosphorylation of nucleoside analogues used as drugs to treat cancer or viral infections. Having different specificities, the characterization of NKs is essential for drug design and nucleotide analogue production in an in vitro enzymatic process. Therefore, a fast and reliable substrate screening method for NKs is of great importance. Here, we report on the validation of a well-known luciferase-based assay for the detection of NK activity in a 96-well plate format. The assay was semi-automated using a liquid handling robot. Good linearity was demonstrated (r² > 0.98) in the range of 0-500 µM ATP, and it was shown that alternative phosphate donors like dATP or CTP were also accepted by the luciferase. The developed high-throughput assay revealed comparable results to HPLC analysis. The assay was exemplarily used for the comparison of the substrate spectra of four NKs using 20 (8 natural, 12 modified) substrates. The screening results correlated well with literature data, and additionally, previously unknown substrates were identified for three of the NKs studied. Our results demonstrate that the developed semi-automated high-throughput assay is suitable to identify best performing NKs for a wide range of substrates.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Phosphotransferases / Nucleosides Type of study: Diagnostic study / Prognostic study Topics: Traditional medicine Limits: Animals / Humans Language: English Year: 2021 Document Type: Article Affiliation country: Ijms222111558

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Phosphotransferases / Nucleosides Type of study: Diagnostic study / Prognostic study Topics: Traditional medicine Limits: Animals / Humans Language: English Year: 2021 Document Type: Article Affiliation country: Ijms222111558