3.9 Article

Development of LC/MS/MS, High-Throughput Enzymatic and Cellular Assays for the Characterization of Compounds That Inhibit Kynurenine Monooxygenase (KMO)

期刊

JOURNAL OF BIOMOLECULAR SCREENING
卷 18, 期 8, 页码 879-889

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/1087057113489731

关键词

kynurenine; 3-hydroxykynurenine; kynurenine 3-monooxygenase; LC/MS/MS; microglia; human PBMCs

资金

  1. CHDI Foundation

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Kynurenine monooxygenase (KMO) catalyzes the conversion of kynurenine to 3-hydroxykynurenine. Modulation of KMO activity has been implicated in several neurodegenerative diseases, including Huntington disease. Our goal is to develop potent and selective small-molecule KMO inhibitors with suitable pharmacokinetic characteristics for in vivo proof-of-concept studies and subsequent clinical development. We developed a comprehensive panel of biochemical and cell-based assays that use liquid chromatography/tandem mass spectrometry to quantify unlabeled kynurenine and 3-hydroxykynurenine. We describe assays to measure KMO inhibition in cell and tissue extracts, as well as cellular assays including heterologous cell lines and primary rat microglia and human peripheral blood mononuclear cells.

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