Literature DB >> 26095399

Förster resonance energy transfer-based cholesterolysis assay identifies a novel hedgehog inhibitor.

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.
Copyright © 2015 Elsevier Inc. All rights reserved.

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


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