| Literature DB >> 27009944 |
Franca-Maria Klingler1, Markus Wolf2, Sandra Wittmann1, Philip Gribbon2, Ewgenij Proschak3.
Abstract
Soluble epoxide hydrolase (sEH) is a bifunctional enzyme that possesses an epoxide hydrolase and lipid phosphatase activity (sEH-P) at two distinct catalytic domains. While the physiological role of the epoxide hydrolase domain is well understood, the consequences of the phosphatase activity remain unclear. Herein we describe the bacterial expression of the recombinant N-terminal domain of sEH-P and the development of a high-throughput screening protocol using a sensitive and commercially available substrate fluorescein diphosphate. The usability of the assay system was demonstrated and novel inhibitors of sEH-P were identified.Entities:
Keywords: enzyme assay; high-throughput screening; phosphatase; soluble epoxide hydrolase
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Year: 2016 PMID: 27009944 DOI: 10.1177/1087057116637609
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571