| Literature DB >> 26095399 |
Timothy S Owen1, George Ngoje1, Travis J Lageman1, Brandon M Bordeau1, Marlene Belfort2, Brian P Callahan3.
Abstract
Hedgehog (Hh) proteins function in cell/cell signaling processes linked to human embryo development and the progression of several types of cancer. Here, we describe an optical assay of hedgehog cholesterolysis, a unique autoprocessing event critical for Hh function. The assay uses a recombinant Förster resonance energy transfer (FRET)-active Hh precursor whose cholesterolysis can be monitored continuously in multi-well plates (dynamic range=4, Z'=0.7), offering advantages in throughput over conventional sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) assays. Application of the optical assay in a pilot small molecule screen produced a novel cholesterolysis inhibitor (apparent IC50=5×10(-6)M) that appears to inactivate hedgehog covalently by a substitution nucleophilic aromatic (SNAr) mechanism.Entities:
Keywords: Cancer; FRET; Fluorescence; Hedgehog protein; Protein engineering; Small molecule screening
Mesh:
Substances:
Year: 2015 PMID: 26095399 PMCID: PMC4591182 DOI: 10.1016/j.ab.2015.06.021
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365