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Development of an HTS-compatible assay for the discovery of ASK1 signalosome inhibitors using alphascreen technology.

Assay and drug development technologies (2014-05-17)
Emmanuel Sturchler, Weimin Chen, Timothy Spicer, Peter Hodder, Patricia McDonald, Derek Duckett
RESUMEN

Genetic target validation studies have demonstrated that the apoptosis signal-regulating kinase 1 (ASK1) represents an important target for the treatment of rheumatoid arthritis, cardiac diseases, and several neurodegenerative disorders. To identify small-molecule inhibitors of ASK1, we have developed a high-throughput screening-compatible, homogenous, biochemical assay using AlphaScreen technology. This novel assay design utilizes purified stress-activated ASK1 signalosome complex, and it monitors phosphorylation of its full-length native substrate, MKK6. The assay has been optimized in a 384-well format and validated by screening the Sigma LOPAC library. The results presented here demonstrate that the assay is sensitive and robust with a Z' factor value of 0.88±0.04 and a signal-to-background ratio of 11, indicating that this assay can be used to screen large chemical libraries to discover novel inhibitors of ASK1.

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Sigma-Aldrich
ANTI-FLAG® M2 monoclonal antibody produced in mouse, clone M2, purified immunoglobulin (Purified IgG1 subclass), buffered aqueous solution (10 mM sodium phosphate, 150 mM NaCl, pH 7.4, containing 0.02% sodium azide)
Sigma-Aldrich
LOPAC®1280
Sigma-Aldrich
LOPAC®1280 - pequeña escala
Sigma-Aldrich
LOPAC®1280 - pequeña escala, International Version
Sigma-Aldrich
LOPAC®1280 (International Version)
Sigma-Aldrich
MKK6/SKK3 Protein, inactive, 50 g, Unactive, recombinant human MKK6, amino acids 4-end, fused at the N-terminus to a Mal-E tag, for use in Kinase Assays.